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Previous release (v1)
2024-04-30 20:48:44, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_017893 4489 bp mRNA linear PRI 27-JUN-2023
DEFINITION Homo sapiens semaphorin 4G (SEMA4G), transcript variant 1, mRNA.
ACCESSION NM_017893
VERSION NM_017893.4
KEYWORDS RefSeq; MANE Select.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1 (bases 1 to 4489)
AUTHORS Shen Z, Sun Y and Niu G.
TITLE Variants in TPO rs2048722, PTCSC2 rs925489 and SEMA4G rs4919510
affect thyroid carcinoma susceptibility risk
JOURNAL BMC Med Genomics 16 (1), 19 (2023)
PUBMED 36737753
REMARK GeneRIF: Variants in TPO rs2048722, PTCSC2 rs925489 and SEMA4G
rs4919510 affect thyroid carcinoma susceptibility risk.
Publication Status: Online-Only
REFERENCE 2 (bases 1 to 4489)
AUTHORS Wu S, Yuan W, Shen Y, Lu X, Li Y, Tian T, Jiang L, Zhuang X, Wu J
and Chu M.
TITLE The miR-608 rs4919510 polymorphism may modify cancer susceptibility
based on type
JOURNAL Tumour Biol 39 (6), 1010428317703819 (2017)
PUBMED 28653886
REMARK GeneRIF: These findings provide evidence that the miR-608 rs4919510
polymorphism may modify cancer susceptibility in a type-specific
manner. Furthermore, SEMA4G may function as an oncogene or tumour
suppressor to regulate tumour development in a type-specific
manner. Further studies with experimental evaluations are
warranted.
REFERENCE 3 (bases 1 to 4489)
AUTHORS Horikawa Y, Wood CG, Yang H, Zhao H, Ye Y, Gu J, Lin J, Habuchi T
and Wu X.
TITLE Single nucleotide polymorphisms of microRNA machinery genes modify
the risk of renal cell carcinoma
JOURNAL Clin Cancer Res 14 (23), 7956-7962 (2008)
PUBMED 19047128
REMARK GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
REFERENCE 4 (bases 1 to 4489)
AUTHORS Grupe A, Li Y, Rowland C, Nowotny P, Hinrichs AL, Smemo S, Kauwe
JS, Maxwell TJ, Cherny S, Doil L, Tacey K, van Luchene R, Myers A,
Wavrant-De Vrieze F, Kaleem M, Hollingworth P, Jehu L, Foy C,
Archer N, Hamilton G, Holmans P, Morris CM, Catanese J, Sninsky J,
White TJ, Powell J, Hardy J, O'Donovan M, Lovestone S, Jones L,
Morris JC, Thal L, Owen M, Williams J and Goate A.
TITLE A scan of chromosome 10 identifies a novel locus showing strong
association with late-onset Alzheimer disease
JOURNAL Am J Hum Genet 78 (1), 78-88 (2006)
PUBMED 16385451
REMARK GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
REFERENCE 5 (bases 1 to 4489)
AUTHORS Deloukas P, Earthrowl ME, Grafham DV, Rubenfield M, French L,
Steward CA, Sims SK, Jones MC, Searle S, Scott C, Howe K, Hunt SE,
Andrews TD, Gilbert JG, Swarbreck D, Ashurst JL, Taylor A, Battles
J, Bird CP, Ainscough R, Almeida JP, Ashwell RI, Ambrose KD,
Babbage AK, Bagguley CL, Bailey J, Banerjee R, Bates K, Beasley H,
Bray-Allen S, Brown AJ, Brown JY, Burford DC, Burrill W, Burton J,
Cahill P, Camire D, Carter NP, Chapman JC, Clark SY, Clarke G, Clee
CM, Clegg S, Corby N, Coulson A, Dhami P, Dutta I, Dunn M, Faulkner
L, Frankish A, Frankland JA, Garner P, Garnett J, Gribble S,
Griffiths C, Grocock R, Gustafson E, Hammond S, Harley JL, Hart E,
Heath PD, Ho TP, Hopkins B, Horne J, Howden PJ, Huckle E, Hynds C,
Johnson C, Johnson D, Kana A, Kay M, Kimberley AM, Kershaw JK,
Kokkinaki M, Laird GK, Lawlor S, Lee HM, Leongamornlert DA, Laird
G, Lloyd C, Lloyd DM, Loveland J, Lovell J, McLaren S, McLay KE,
McMurray A, Mashreghi-Mohammadi M, Matthews L, Milne S, Nickerson
T, Nguyen M, Overton-Larty E, Palmer SA, Pearce AV, Peck AI, Pelan
S, Phillimore B, Porter K, Rice CM, Rogosin A, Ross MT, Sarafidou
T, Sehra HK, Shownkeen R, Skuce CD, Smith M, Standring L, Sycamore
N, Tester J, Thorpe A, Torcasso W, Tracey A, Tromans A, Tsolas J,
Wall M, Walsh J, Wang H, Weinstock K, West AP, Willey DL, Whitehead
SL, Wilming L, Wray PW, Young L, Chen Y, Lovering RC, Moschonas NK,
Siebert R, Fechtel K, Bentley D, Durbin R, Hubbard T,
Doucette-Stamm L, Beck S, Smith DR and Rogers J.
TITLE The DNA sequence and comparative analysis of human chromosome 10
JOURNAL Nature 429 (6990), 375-381 (2004)
PUBMED 15164054
REFERENCE 6 (bases 1 to 4489)
AUTHORS Pasterkamp RJ and Kolodkin AL.
TITLE Semaphorin junction: making tracks toward neural connectivity
JOURNAL Curr Opin Neurobiol 13 (1), 79-89 (2003)
PUBMED 12593985
REMARK Review article
REFERENCE 7 (bases 1 to 4489)
AUTHORS Dickson BJ.
TITLE Molecular mechanisms of axon guidance
JOURNAL Science 298 (5600), 1959-1964 (2002)
PUBMED 12471249
REMARK Review article
Erratum:[Science. 2003 Jan 24;299(5606):515]
REFERENCE 8 (bases 1 to 4489)
AUTHORS Holtmaat AJ, De Winter F, De Wit J, Gorter JA, da Silva FH and
Verhaagen J.
TITLE Semaphorins: contributors to structural stability of hippocampal
networks?
JOURNAL Prog Brain Res 138, 17-38 (2002)
PUBMED 12432760
REMARK Review article
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from AL133215.17.
On Mar 23, 2021 this sequence version replaced NM_017893.3.
Summary: Semaphorins are a large family of conserved secreted and
membrane associated proteins which possess a semaphorin (Sema)
domain and a PSI domain (found in plexins, semaphorins and
integrins) in the N-terminal extracellular portion. Based on
sequence and structural similarities, semaphorins are put into
eight classes: invertebrates contain classes 1 and 2, viruses have
class V, and vertebrates contain classes 3-7. Semaphorins serve as
axon guidance ligands via multimeric receptor complexes, some (if
not all) containing plexin proteins. Multiple transcript variants
encoding different isoforms have been found for this gene.
[provided by RefSeq, Feb 2011].
Transcript Variant: This variant (1) encodes the longest isoform
(1).
##Evidence-Data-START##
Transcript exon combination :: SRR14038191.1499729.1,
SRR14038195.2065170.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
SAMEA1968540, SAMEA1968832
[ECO:0000348]
##Evidence-Data-END##
##RefSeq-Attributes-START##
MANE Ensembl match :: ENST00000210633.4/ ENSP00000210633.3
RefSeq Select criteria :: based on manual assertion, conservation,
longest protein
##RefSeq-Attributes-END##
COMPLETENESS: full length.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-88 AL133215.17 52328-52415
89-596 AL133215.17 55353-55860
597-745 AL133215.17 55953-56101
746-808 AL133215.17 56371-56433
809-907 AL133215.17 60456-60554
908-1001 AL133215.17 61119-61212
1002-1115 AL133215.17 61351-61464
1116-1285 AL133215.17 61673-61842
1286-1455 AL133215.17 61926-62095
1456-1600 AL133215.17 62672-62816
1601-1823 AL133215.17 62946-63168
1824-1939 AL133215.17 63402-63517
1940-2115 AL133215.17 63646-63821
2116-2177 AL133215.17 63992-64053
2178-4489 AL133215.17 66129-68440
FEATURES Location/Qualifiers
source 1..4489
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="10"
/map="10q24.31"
gene 1..4489
/gene="SEMA4G"
/note="semaphorin 4G"
/db_xref="GeneID:57715"
/db_xref="HGNC:HGNC:10735"
/db_xref="MIM:618991"
exon 1..88
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 1..2
/gene="SEMA4G"
/replace=""
/replace="ag"
/db_xref="dbSNP:1467940472"
variation 1
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1194222240"
variation 2
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1253674040"
variation 3
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1375312685"
variation 4
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850567705"
variation 5
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1479078047"
variation 6
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1296202088"
variation 7
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:991345198"
variation 8
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133849907"
variation 10
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1408262006"
variation 11
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850567967"
variation 12
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1370130694"
variation 13..14
/gene="SEMA4G"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1589975880"
variation 13
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1589975877"
variation 14
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133849925"
variation 17
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1174345519"
variation 22..29
/gene="SEMA4G"
/replace="cagctggt"
/replace="cagctggtcagctggt"
/db_xref="dbSNP:1419154452"
variation 26
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850568268"
variation 27
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1410747126"
variation 28
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:866504226"
variation 30
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1436737403"
variation 32
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1393334579"
variation 33..41
/gene="SEMA4G"
/replace="gtggggccg"
/replace="gtggggccgtggggccg"
/db_xref="dbSNP:1850568583"
variation 35..38
/gene="SEMA4G"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:2133849963"
variation 39
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1005296035"
variation 42
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850568737"
variation 44
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850568792"
variation 45
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133849980"
variation 46
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850568859"
variation 47
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850568916"
variation 48..53
/gene="SEMA4G"
/replace="cg"
/replace="cgcgcg"
/db_xref="dbSNP:1850569061"
variation 48
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:917174896"
variation 50
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1175789338"
variation 53
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1392762963"
variation 63
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1461341188"
variation 64
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850569329"
variation 65
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1212560086"
variation 66
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850569479"
variation 68
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1589975902"
variation 71
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850569628"
variation 72
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850569699"
variation 73
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:546087970"
variation 75
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1254875583"
variation 78
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:982522207"
variation 79
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1332295021"
variation 80
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133850056"
variation 81
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850570085"
variation 82
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850570148"
variation 83
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:557633516"
variation 84
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850570281"
variation 85
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:374064553"
variation 86
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:922120937"
variation 87
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133850081"
exon 89..596
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 93
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1030762196"
variation 94
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850663596"
variation 98
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850663843"
variation 100
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850663913"
variation 101
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:557949623"
variation 113
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1335694004"
variation 116
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1457386306"
variation 117
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850664129"
variation 124
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1365050521"
variation 125
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850664254"
variation 126
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:892265119"
variation 127
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:570166640"
variation 128
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1414497874"
variation 129
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:867026643"
variation 130
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1394108765"
variation 131
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850664603"
variation 132
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:943019392"
variation 133
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:761543704"
variation 137
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1589978234"
variation 142
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:537435528"
variation 148
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:60278872"
variation 150
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:111933864"
variation 152
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1262698358"
variation 153
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850665019"
variation 154
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850665075"
variation 159
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1850665124"
variation 166
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1213813489"
variation 171
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850665221"
variation 178
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1316377096"
variation 181
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:980739677"
variation 185
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:182450988"
variation 186
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850665375"
variation 187
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850665422"
variation 188
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1589978258"
variation 190
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1034747287"
variation 192
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1449004233"
variation 195
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1589978265"
variation 200
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850665683"
variation 203
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1381078635"
variation 207
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850665781"
variation 209
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:934446804"
variation 211
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:960088474"
variation 216
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850665939"
variation 218..219
/gene="SEMA4G"
/replace=""
/replace="gtg"
/db_xref="dbSNP:1850666070"
variation 218
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:115583289"
variation 219
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850666120"
variation 220
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1386772616"
variation 223
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1850666516"
variation 234..238
/gene="SEMA4G"
/replace="ct"
/replace="cttct"
/db_xref="dbSNP:1330691442"
variation 242
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850666602"
variation 246
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850666651"
variation 251..254
/gene="SEMA4G"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:771249674"
variation 254
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1286727183"
variation 257
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1234279287"
variation 259
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850666856"
variation 261
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850666906"
variation 267
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:747642385"
variation 269
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1850667028"
variation 272..274
/gene="SEMA4G"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1365607676"
variation 281
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1850667141"
variation 282
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:553501059"
variation 285
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850667233"
variation 288..293
/gene="SEMA4G"
/replace="ccccc"
/replace="cccccc"
/replace="ccccccc"
/db_xref="dbSNP:1276939230"
variation 288
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850667277"
variation 289
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:578092859"
variation 293
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:949932767"
variation 294
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1044290858"
variation 298
/gene="SEMA4G"
/replace="c"
/replace="ctgc"
/db_xref="dbSNP:1850667555"
variation 304..309
/gene="SEMA4G"
/replace="cccccc"
/replace="ccccccc"
/db_xref="dbSNP:1198554590"
variation 304
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1259348483"
variation 305
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1485595178"
variation 307
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:186703368"
variation 310
/gene="SEMA4G"
/replace=""
/replace="a"
/db_xref="dbSNP:1850667867"
variation 310
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:973566758"
variation 311
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1207497990"
variation 313
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1358003866"
variation 318
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850668057"
variation 319
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1807570131"
variation 319
/gene="SEMA4G"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1807570306"
variation 325
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850668128"
variation 326
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850668209"
variation 329
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850668271"
variation 332
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1266084809"
variation 338
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1451781054"
variation 343
/gene="SEMA4G"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1328543428"
variation 343
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1293029193"
misc_feature 344..346
/gene="SEMA4G"
/note="upstream in-frame stop codon"
variation 345
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1381265281"
variation 347
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1345600213"
variation 349
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850668683"
variation 350
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850668734"
variation 351
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1304369840"
variation 354
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:905793660"
variation 355
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850668844"
variation 364
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:560469443"
variation 369
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850668946"
variation 370
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:563225955"
variation 373
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850669047"
variation 379
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850669092"
variation 381
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1364956082"
variation 384
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1168394557"
variation 386
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:1850669406"
variation 386
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:771649939"
variation 391
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1371109660"
variation 393
/gene="SEMA4G"
/replace=""
/replace="g"
/db_xref="dbSNP:1850669696"
variation 395
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1191340004"
variation 396
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1050718409"
variation 401
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1477407403"
variation 405
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:890089013"
variation 406
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850670117"
variation 408
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1016975985"
variation 409
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1442004696"
variation 410
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1269856612"
variation 411
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850670356"
variation 414
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:897234872"
variation 416
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:944394849"
variation 417
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1268862242"
variation 418
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1052574006"
variation 426
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:192621867"
variation 428
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:752393071"
variation 430
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1564791838"
variation 431
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850671019"
variation 433
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850671101"
variation 434..436
/gene="SEMA4G"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1850671316"
variation 434
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1224898784"
variation 436
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:867629405"
variation 438
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1250557337"
variation 440..444
/gene="SEMA4G"
/replace="ggggg"
/replace="gggggg"
/db_xref="dbSNP:1345238361"
variation 440
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:758309995"
variation 441
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:777690359"
variation 443..445
/gene="SEMA4G"
/replace="ggt"
/replace="ggtggt"
/db_xref="dbSNP:1850671886"
variation 444
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:746967585"
variation 446
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:770865272"
variation 447..448
/gene="SEMA4G"
/replace=""
/replace="tt"
/db_xref="dbSNP:1850672187"
variation 447
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:781140045"
variation 454
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1010644581"
variation 460
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1430821467"
variation 464
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850672377"
variation 469
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1402602510"
CDS 473..3004
/gene="SEMA4G"
/note="isoform 1 precursor is encoded by transcript
variant 1; sema domain, immunoglobulin domain (Ig),
transmembrane domain (TM) and short cytoplasmic domain,
(semaphorin) 4G"
/codon_start=1
/product="semaphorin-4G isoform 1 precursor"
/protein_id="NP_060363.2"
/db_xref="CCDS:CCDS7501.1"
/db_xref="GeneID:57715"
/db_xref="HGNC:HGNC:10735"
/db_xref="MIM:618991"
/translation="
MWGRLWPLLLSILTATAVPGPSLRRPSRELDATPRMTIPYEELSGTRHFKGQAQNYSTLLLEEASARLLVGARGALFSLSANDIGDGAHKEIHWEASPEMQSKCHQKGKNNQTECFNHVRFLQRLNSTHLYACGTHAFQPLCAAIDAEAFTLPTSFEEGKEKCPYDPARGFTGLIIDGGLYTATRYEFRSIPDIRRSRHPHSLRTEETPMHWLNDAEFVFSVLVRESKASAVGDDDKVYYFFTERATEEGSGSFTQSRSSHRVARVARVCKGDLGGKKILQKKWTSFLKARLICHIPLYETLRGVCSLDAETSSRTHFYAAFTLSTQWKTLEASAICRYDLAEIQAVFAGPYMEYQDGSRRWGRYEGGVPEPRPGSCITDSLRSQGYNSSQDLPSLVLDFVKLHPLMARPVVPTRGRPLLLKRNIRYTHLTGTPVTTPAGPTYDLLFLGTADGWIHKAVVLGSGMHIIEETQVFRESQSVENLVISLLQHSLYVGAPSGVIQLPLSSCSRYRSCYDCILARDPYCGWDPGTHACAAATTIANRSQGSRTALIQDIERGNRGCESSRDTGPPPPLKTRSVLRGDDVLLPCDQPSNLARALWLLNGSMGLSDGQGGYRVGVDGLLVTDAQPEHSGNYGCYAEENGLRTLLASYSLTVRPATPAPAPKAPATPGAQLAPDVRLLYVLAIAALGGLCLILASSLLYVACLREGRRGRRRKYSLGRASRAGGSAVQLQTVSGQCPGEEDEGDDEGAGGLEGSCLQIIPGEGAPAPPPPPPPPPPAELTNGLVALPSRLRRMNGNSYVLLRQSNNGVPAGPCSFAEELSRILEKRKHTQLVEQLDESSV"
sig_peptide 473..523
/gene="SEMA4G"
/inference="COORDINATES: ab initio prediction:SignalP:4.0"
misc_feature 611..1990
/gene="SEMA4G"
/note="The Sema domain, a protein interacting module, of
semaphorin 4G (Sema4G); Region: Sema_4G; cd11262"
/db_xref="CDD:200523"
misc_feature 635..637
/gene="SEMA4G"
/note="N-linked (GlcNAc...) asparagine.
/evidence=ECO:0000255; propagated from
UniProtKB/Swiss-Prot (Q9NTN9.1); glycosylation site"
misc_feature order(788..796,965..967,1028..1030,1034..1042,1085..1087,
1094..1096,1100..1102,1115..1117,1211..1213,1301..1315,
1319..1321,1547..1552,1655..1657,1667..1669,1676..1678)
/gene="SEMA4G"
/note="plexin binding site [polypeptide binding]; other
site"
/db_xref="CDD:200523"
misc_feature 803..805
/gene="SEMA4G"
/note="N-linked (GlcNAc...) asparagine.
/evidence=ECO:0000255; propagated from
UniProtKB/Swiss-Prot (Q9NTN9.1); glycosylation site"
misc_feature 848..850
/gene="SEMA4G"
/note="N-linked (GlcNAc...) asparagine.
/evidence=ECO:0000255; propagated from
UniProtKB/Swiss-Prot (Q9NTN9.1); glycosylation site"
misc_feature order(1214..1219,1241..1243,1250..1258,1358..1360,
1367..1375,1379..1381,1385..1387,1442..1444,1451..1456,
1466..1471,1694..1696,1739..1741)
/gene="SEMA4G"
/note="putative homodimer interface [polypeptide binding];
other site"
/db_xref="CDD:200523"
misc_feature 1634..1636
/gene="SEMA4G"
/note="N-linked (GlcNAc...) asparagine.
/evidence=ECO:0000255; propagated from
UniProtKB/Swiss-Prot (Q9NTN9.1); glycosylation site"
misc_feature 1991..>2074
/gene="SEMA4G"
/note="Plexin repeat; Region: PSI; pfam01437"
/db_xref="CDD:396154"
misc_feature 2096..2098
/gene="SEMA4G"
/note="N-linked (GlcNAc...) asparagine.
/evidence=ECO:0000255; propagated from
UniProtKB/Swiss-Prot (Q9NTN9.1); glycosylation site"
misc_feature 2186..2437
/gene="SEMA4G"
/note="Immunoglobulin (Ig)-like domain of the class IV
semaphorin Sema4B; Region: Ig_Sema4B_like; cd05872"
/db_xref="CDD:409456"
misc_feature 2186..2206
/gene="SEMA4G"
/note="Ig strand A [structural motif]; Region: Ig strand
A"
/db_xref="CDD:409456"
misc_feature 2216..2242
/gene="SEMA4G"
/note="Ig strand B [structural motif]; Region: Ig strand
B"
/db_xref="CDD:409456"
misc_feature order(2222..2224,2345..2347)
/gene="SEMA4G"
/note="dimer interface [polypeptide binding]; other site"
/db_xref="CDD:409456"
misc_feature 2258..2278
/gene="SEMA4G"
/note="Ig strand C [structural motif]; Region: Ig strand
C"
/db_xref="CDD:409456"
misc_feature 2279..2281
/gene="SEMA4G"
/note="N-linked (GlcNAc...) asparagine.
/evidence=ECO:0000255; propagated from
UniProtKB/Swiss-Prot (Q9NTN9.1); glycosylation site"
misc_feature 2282..2293
/gene="SEMA4G"
/note="Ig strand C' [structural motif]; Region: Ig strand
C'"
/db_xref="CDD:409456"
misc_feature 2312..2326
/gene="SEMA4G"
/note="Ig strand D [structural motif]; Region: Ig strand
D"
/db_xref="CDD:409456"
misc_feature 2330..2353
/gene="SEMA4G"
/note="Ig strand E [structural motif]; Region: Ig strand
E"
/db_xref="CDD:409456"
misc_feature 2369..2398
/gene="SEMA4G"
/note="Ig strand F [structural motif]; Region: Ig strand
F"
/db_xref="CDD:409456"
misc_feature 2513..2575
/gene="SEMA4G"
/note="propagated from UniProtKB/Swiss-Prot (Q9NTN9.1);
transmembrane region"
misc_feature 2654..2818
/gene="SEMA4G"
/note="propagated from UniProtKB/Swiss-Prot (Q9NTN9.1);
Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite"
misc_feature 2870..2872
/gene="SEMA4G"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:23186163; propagated from
UniProtKB/Swiss-Prot (Q9NTN9.1); phosphorylation site"
misc_feature 2996..2998
/gene="SEMA4G"
/note="Phosphoserine.
/evidence=ECO:0000250|UniProtKB:Q9WUH7; propagated from
UniProtKB/Swiss-Prot (Q9NTN9.1); phosphorylation site"
variation 473
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1191397762"
variation 475
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1344292943"
variation 476..499
/gene="SEMA4G"
/replace=""
/replace="tgggggaggctctggcccctcctc"
/db_xref="dbSNP:1564791884"
variation 477..481
/gene="SEMA4G"
/replace="ggggg"
/replace="gggggg"
/db_xref="dbSNP:1850672932"
variation 477
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:745907076"
variation 478
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:769754047"
variation 481
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850673074"
variation 487
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1393022504"
variation 490
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:775751808"
variation 492
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1043525758"
variation 493
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1167174298"
variation 502
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850673445"
variation 507
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:1850673633"
variation 507
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:763127413"
variation 511
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:141766082"
variation 512
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1850673834"
variation 513
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1469347701"
variation 515
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:201769907"
variation 516
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1363910803"
variation 518
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850674227"
variation 519
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:762257142"
variation 521
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850674430"
variation 522
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:768000743"
variation 523
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:753300939"
variation 524
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:765633702"
variation 526
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:528334576"
variation 534
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:764810125"
variation 535
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1322465491"
variation 537
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:752448070"
variation 540
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1261974981"
variation 542
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:150563616"
variation 543
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:751304450"
variation 544
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133857417"
variation 545
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850675630"
variation 548
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1195652118"
variation 549
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:139918504"
variation 550
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:571547734"
variation 551
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850676089"
variation 554
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850676178"
variation 557
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1202124518"
variation 559
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133857469"
variation 562
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:532192623"
variation 563
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:780081656"
variation 565
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:2133857483"
variation 567
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:867204232"
variation 568
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1159955320"
variation 575
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:749532175"
variation 576
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:768824226"
variation 579
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1850677171"
variation 581
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850677263"
variation 584
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:774700812"
variation 587
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:369789414"
variation 590
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:962113918"
variation 591..594
/gene="SEMA4G"
/replace="a"
/replace="atga"
/db_xref="dbSNP:1406530664"
variation 591
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:772310279"
variation 592
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1344402684"
variation 593
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378220105"
variation 594
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133857555"
exon 597..745
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 603
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:369353258"
variation 610
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:144341151"
variation 611
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:372839640"
variation 612
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1370809407"
variation 614
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:780136613"
variation 620
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:913597081"
variation 623
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:749297787"
variation 626
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1441420061"
variation 630
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:755205395"
variation 631
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850682502"
variation 634
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1360751746"
variation 640
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850682665"
variation 642
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1248834281"
variation 644
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850682797"
variation 645
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850682873"
variation 646
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1284517077"
variation 647
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:779253360"
variation 650
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:748287481"
variation 652
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1205748549"
variation 655..662
/gene="SEMA4G"
/replace="ggagg"
/replace="ggaggagg"
/db_xref="dbSNP:1850683258"
variation 656
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1234802535"
variation 659
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:199970914"
variation 661
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:756103359"
variation 666
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:747581175"
variation 670
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850683769"
variation 673
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1029721556"
variation 677
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1243856800"
variation 679
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1446315165"
variation 684
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:376810147"
variation 685
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1384733681"
variation 686
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1384572205"
variation 689
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:750643700"
variation 690
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:202147105"
variation 693
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1007038634"
variation 694
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1589978805"
variation 696
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1352343381"
variation 697
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1402573417"
variation 702..709
/gene="SEMA4G"
/replace="tctctc"
/replace="tctctctc"
/db_xref="dbSNP:1441071018"
variation 704
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850685194"
variation 705
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:199688982"
variation 707
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850685355"
variation 711
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:762606692"
variation 718
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:146573432"
variation 719
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:140040145"
variation 727
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1445693261"
variation 730
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850685679"
variation 732
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:761353685"
variation 733
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1387484882"
variation 734
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1056746530"
variation 738
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:373053309"
variation 741
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:750147136"
variation 743
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:760612775"
exon 746..808
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 751
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:765388169"
variation 752
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1385079315"
variation 758
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:200094625"
variation 760
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:879452513"
variation 761
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:752650927"
variation 762..765
/gene="SEMA4G"
/replace="c"
/replace="cccc"
/db_xref="dbSNP:1589979126"
variation 763
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:149776999"
variation 766
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:891205288"
variation 769
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1423146487"
variation 773
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850694572"
variation 779..781
/gene="SEMA4G"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1457139894"
variation 779
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1257694646"
variation 784
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:751823274"
variation 787
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1224318002"
variation 789..793
/gene="SEMA4G"
/replace="aaaaa"
/replace="aaaaaa"
/db_xref="dbSNP:769978574"
variation 789
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:757731950"
variation 790
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:368462093"
variation 797
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1221941297"
variation 802
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1274539366"
variation 804
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:746403415"
variation 806
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1056293944"
exon 809..907
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 809
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1433192968"
variation 810
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:374837913"
variation 811..812
/gene="SEMA4G"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1564794259"
variation 811
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:368885285"
variation 814
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1488741560"
variation 817
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850858994"
variation 822
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:759972554"
variation 823
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1311071149"
variation 824
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:765790226"
variation 826
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:371741444"
variation 827
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:756797401"
variation 829
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:941992758"
variation 830
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:145690277"
variation 831
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:750061929"
variation 832
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850859667"
variation 833
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564794293"
variation 838
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850859891"
variation 840
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1259506525"
variation 841
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:560293126"
variation 842..852
/gene="SEMA4G"
/replace="c"
/replace="cggctcaattc"
/db_xref="dbSNP:1850860190"
variation 842
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:893274055"
variation 843
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:749056930"
variation 844
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1370695015"
variation 848
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:768561807"
variation 854
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:779061181"
variation 856
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1432659738"
variation 858
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1589984551"
variation 859
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:921297403"
variation 860
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850860820"
variation 862
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:748069351"
variation 865
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850860959"
variation 866
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:376189318"
variation 870
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:932716016"
variation 872
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:751439655"
variation 874
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:772327550"
variation 879
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:572662465"
variation 880
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:760573069"
variation 881
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1406589169"
variation 883
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850861612"
variation 885
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1300897600"
variation 887
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133871074"
variation 889
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850861780"
variation 890
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1295606625"
variation 892
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1413321602"
variation 893..896
/gene="SEMA4G"
/replace="ct"
/replace="ctct"
/db_xref="dbSNP:1438510738"
variation 893
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1366536028"
variation 895
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850862143"
variation 898
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1400263197"
variation 903
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1340182509"
variation 904..905
/gene="SEMA4G"
/replace="ca"
/replace="caca"
/db_xref="dbSNP:764948073"
variation 905
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850862460"
variation 906
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850862536"
exon 908..1001
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 908
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1004659697"
variation 910
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1205461904"
variation 916
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:746066448"
variation 917
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:770161568"
variation 918
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:149008935"
variation 924
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:764608308"
variation 928
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1446373763"
variation 933
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:887525390"
variation 935
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133873792"
variation 936
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:151095552"
variation 937
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:963256942"
variation 939
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:774709885"
variation 940
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:74154244"
variation 941
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:779530961"
variation 945
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:748582901"
variation 946
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:753596253"
variation 947
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1362954670"
variation 948
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1336829326"
variation 951..955
/gene="SEMA4G"
/replace="ag"
/replace="aggag"
/db_xref="dbSNP:768692347"
variation 952
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:374443024"
variation 953
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:752480989"
variation 955
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:758114685"
variation 957
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1215594471"
variation 959
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1564794890"
variation 960
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:758664453"
variation 965
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1326652882"
variation 967
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1316309086"
variation 968
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1198014436"
variation 975
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:746889193"
variation 977
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:140978394"
variation 978
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:201619012"
variation 980
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1589985904"
variation 981
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1236872889"
variation 984
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:934729093"
variation 989
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850892374"
variation 990
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850892457"
variation 994
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:746116241"
variation 995
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1420941687"
variation 996
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1477311108"
variation 998
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:769933802"
variation 1000
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:775849846"
exon 1002..1115
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 1002
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1242205501"
variation 1003
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850902998"
variation 1006
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:749483446"
variation 1007..1008
/gene="SEMA4G"
/replace="g"
/replace="gg"
/db_xref="dbSNP:750452775"
variation 1007
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:769114862"
variation 1008
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1444498751"
variation 1009
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:948989926"
variation 1010
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1352712085"
variation 1011
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1850903953"
variation 1016
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:202220509"
variation 1017
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:773841551"
variation 1018
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:759183570"
variation 1019
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:769395836"
variation 1026
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:775330142"
variation 1029
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:762461498"
variation 1037
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:370387075"
variation 1038
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:751241762"
variation 1041
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1419465318"
variation 1043..1045
/gene="SEMA4G"
/replace="att"
/replace="attatt"
/db_xref="dbSNP:760677059"
variation 1044
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564795185"
variation 1045
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1589986519"
variation 1052
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1393099586"
variation 1053
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1589986527"
variation 1054..1067
/gene="SEMA4G"
/replace="ccgcc"
/replace="ccgccggagccgcc"
/db_xref="dbSNP:1392548033"
variation 1055
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:188609242"
variation 1056
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:375357185"
variation 1058
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:200186312"
variation 1059
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:756229401"
variation 1061
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1375680753"
variation 1062
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850905942"
variation 1064
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:534321099"
variation 1065
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:780089392"
variation 1067
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:374506045"
variation 1069
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1850906271"
variation 1070
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1159156117"
variation 1073
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:759497574"
variation 1074
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1246356373"
variation 1075
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:554197284"
variation 1077
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:142527271"
variation 1079..1080
/gene="SEMA4G"
/replace=""
/replace="ct"
/db_xref="dbSNP:765930905"
variation 1081
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:192790321"
variation 1087
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:753223422"
variation 1087
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133875208"
variation 1088..1093
/gene="SEMA4G"
/replace="gag"
/replace="gaggag"
/db_xref="dbSNP:1439037196"
variation 1090
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:755117958"
variation 1098
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:779341258"
variation 1099
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1181223858"
variation 1100
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1439657511"
variation 1103
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:954618111"
variation 1105
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1184542680"
variation 1112
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:748404181"
exon 1116..1285
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 1117
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:374767509"
variation 1119
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:369471768"
variation 1120
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:145899563"
variation 1122
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1319299438"
variation 1123
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:768211235"
variation 1128
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1461931758"
variation 1129
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1392770440"
variation 1135
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:562278554"
variation 1136
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:138710515"
variation 1141
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:772951663"
variation 1142
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:528948930"
variation 1145
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:760610802"
variation 1146
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:371666695"
variation 1147
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1178341036"
variation 1148
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1303651661"
variation 1152
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1208157981"
variation 1153
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:907505061"
variation 1156
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1316488117"
variation 1157
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:759573797"
variation 1163
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1465509378"
variation 1165
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:765335147"
variation 1166
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1452714855"
variation 1169
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1292595629"
variation 1174
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:752884133"
variation 1175
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:758650850"
variation 1177
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:940372860"
variation 1178..1180
/gene="SEMA4G"
/replace=""
/replace="gac"
/db_xref="dbSNP:1850922975"
variation 1181
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1297186803"
variation 1183
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1037811860"
variation 1188
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1356018019"
variation 1190
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1387941598"
variation 1192..1198
/gene="SEMA4G"
/replace="cttc"
/replace="cttcttc"
/db_xref="dbSNP:1298602317"
variation 1194
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1329808982"
variation 1195
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1233131910"
variation 1198
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:751912530"
variation 1200
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:540792779"
variation 1201
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:781655724"
variation 1205
/gene="SEMA4G"
/replace=""
/replace="c"
/db_xref="dbSNP:781528969"
variation 1205
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:898907623"
variation 1206
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:775552640"
variation 1213
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:754499823"
variation 1217
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:199950454"
variation 1219
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:142733326"
variation 1221
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850925211"
variation 1225
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133876712"
variation 1227
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1179175680"
variation 1229
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:771647101"
variation 1237
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1382158574"
variation 1238
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850925617"
variation 1244
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:773006606"
variation 1245
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:201790937"
variation 1247
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850926055"
variation 1249
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:919007889"
variation 1255..1272
/gene="SEMA4G"
/replace="ccgtgtggc"
/replace="ccgtgtggcccgtgtggc"
/db_xref="dbSNP:746431273"
variation 1255
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:868505946"
variation 1256
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:770726629"
variation 1257
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:551004768"
variation 1259
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1389345205"
variation 1260
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:759469028"
variation 1265..1278
/gene="SEMA4G"
/replace="cgtgtggctcgtgt"
/replace="cgtgtggctcgtgtggctcgtgt"
/db_xref="dbSNP:1850927374"
variation 1265
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:765262844"
variation 1266
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:377151700"
variation 1267
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:763278051"
variation 1270
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:764466706"
variation 1271
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:751824969"
variation 1274
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:888912092"
variation 1275
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1224011022"
variation 1276
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:118166648"
variation 1278
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:767904665"
variation 1284
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1850928191"
variation 1285
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1199366181"
exon 1286..1455
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 1286
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:2133877724"
variation 1287
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:200202967"
variation 1289
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:762050264"
variation 1291
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1170863177"
variation 1292
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133877770"
variation 1293
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:137857983"
variation 1294..1296
/gene="SEMA4G"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1850933595"
variation 1296
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:866490784"
variation 1298
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133877805"
variation 1299
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133877813"
variation 1300
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850933809"
variation 1302
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133877834"
variation 1303
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1238045368"
variation 1304
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133877862"
variation 1306
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:961966703"
variation 1307
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133877885"
variation 1309
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133877896"
variation 1311
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:1850934122"
variation 1311
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133877909"
variation 1313
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133877929"
variation 1314..1321
/gene="SEMA4G"
/replace="agaag"
/replace="agaagaag"
/db_xref="dbSNP:1179910574"
variation 1314
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133877937"
variation 1315
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:750733650"
variation 1316
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133877972"
variation 1317
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1850934544"
variation 1318
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:149549143"
variation 1319
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1850934768"
variation 1320
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133878008"
variation 1321
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:766970037"
variation 1322
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133878023"
variation 1323
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133878031"
variation 1326
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133878041"
variation 1327
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:144136150"
variation 1328
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133878063"
variation 1330
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133878069"
variation 1331
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850935025"
variation 1332
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:2133878084"
variation 1334
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133878090"
variation 1337
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133878099"
variation 1340
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:2133878106"
variation 1341
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133878118"
variation 1343
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:954409603"
variation 1344
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:374601814"
variation 1346
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:908122906"
variation 1348
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133878155"
variation 1349
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1329807522"
variation 1353
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133878172"
variation 1354
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564795878"
variation 1355
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133878196"
variation 1356
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:777213392"
variation 1357
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:751242836"
variation 1359
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133878218"
variation 1360
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133878227"
variation 1362
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133878231"
variation 1363
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:188155769"
variation 1365
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:138709087"
variation 1367
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:780858350"
variation 1368
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:141723515"
variation 1372
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:2133878282"
variation 1373
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850935891"
variation 1374
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:201040570"
variation 1375
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:200499542"
variation 1378
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1372311283"
variation 1379
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:576159833"
variation 1380
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:376301016"
variation 1384
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1413942825"
variation 1389
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850936462"
variation 1395
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:774536639"
variation 1399
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1313882295"
variation 1402
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1207707838"
variation 1406
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:943187702"
variation 1412
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:767392247"
variation 1413
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1161933809"
variation 1414
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:761950373"
variation 1415
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:772280066"
variation 1416
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:749963260"
variation 1417
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1235341225"
variation 1419
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:761169377"
variation 1421
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:766701174"
variation 1423
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:754363609"
variation 1424
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850937754"
variation 1427
/gene="SEMA4G"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1426443730"
variation 1429
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:759995340"
variation 1430
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:370799129"
variation 1440
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:755545765"
variation 1441
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:374213077"
variation 1442
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1420759299"
variation 1444
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1313225853"
variation 1445
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133878596"
variation 1447
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133878605"
variation 1448
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133878615"
variation 1450
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:146235728"
variation 1454
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:767264493"
exon 1456..1600
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 1456
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1473090285"
variation 1458
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:184755985"
variation 1460
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1589989813"
variation 1461
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:142303289"
variation 1462
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413764190"
variation 1463
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:200241224"
variation 1467
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1850976356"
variation 1469
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:764921000"
variation 1470
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1216318709"
variation 1471
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:752708818"
variation 1476
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:758200614"
variation 1478
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1161211887"
variation 1482
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1201341797"
variation 1484
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:369063086"
variation 1485
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:751695050"
variation 1487
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850977775"
variation 1488
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1187494537"
variation 1490
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1589989912"
variation 1493
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850978202"
variation 1496
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1264248737"
variation 1497
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1589989925"
variation 1501
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:964354750"
variation 1502
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1850978747"
variation 1507
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:190271357"
variation 1508
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1372385660"
variation 1510
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:757320010"
variation 1512
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:376797424"
variation 1513
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850979346"
variation 1514
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:150824972"
variation 1515
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1240413142"
variation 1516
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1193173688"
variation 1518
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1399753855"
variation 1521
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850979819"
variation 1522
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1433937750"
variation 1523..1525
/gene="SEMA4G"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1452660752"
variation 1523
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:780443579"
variation 1525
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:367883776"
variation 1528
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:770163597"
variation 1530
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1342003827"
variation 1538
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1397546136"
variation 1539
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:372466257"
variation 1540
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850980546"
variation 1541
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:749809765"
variation 1543
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:376969087"
variation 1545
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850980816"
variation 1547
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1229991911"
variation 1548..1550
/gene="SEMA4G"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:35989286"
variation 1548
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1339531318"
variation 1550
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:988692457"
variation 1551
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:774913495"
variation 1553
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:199762950"
variation 1554
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:553537753"
variation 1557
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850981685"
variation 1558
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:776474084"
variation 1560
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:759217416"
variation 1562
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1261099304"
variation 1563
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:199677082"
variation 1565
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1200907162"
variation 1566
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:752375155"
variation 1570
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:577628245"
variation 1572
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:764005138"
variation 1573
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:751463430"
variation 1574
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:781196938"
variation 1576
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:750677818"
variation 1577
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1390825588"
variation 1579
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1388071510"
variation 1581
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850983227"
variation 1582
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:756226933"
variation 1583
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:965691185"
variation 1588
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1365199089"
variation 1589
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:949989449"
variation 1590
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:147630038"
variation 1599
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:749676557"
variation 1600
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:768865327"
exon 1601..1823
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 1601
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:775053317"
variation 1610
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850994061"
variation 1612..1613
/gene="SEMA4G"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1564796771"
variation 1614
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1850994366"
variation 1617
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:748920327"
variation 1619
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:761554973"
variation 1620
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:774063487"
variation 1624
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850994826"
variation 1625
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:761753573"
variation 1635
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:917222193"
variation 1640
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1850995253"
variation 1642
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1210217429"
variation 1643
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1354888744"
variation 1644
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1564796809"
variation 1645..1651
/gene="SEMA4G"
/replace=""
/replace="agacttg"
/db_xref="dbSNP:1564796818"
variation 1646
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:767502487"
variation 1648
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:773129383"
variation 1651
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:760713409"
variation 1652
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1203491941"
variation 1653
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:766463475"
variation 1659
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850996705"
variation 1660
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1471143694"
variation 1661
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:754033511"
variation 1662
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850996981"
variation 1664
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1290463761"
variation 1666
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:755190563"
variation 1669
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:765708793"
variation 1675
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:971229127"
variation 1678..1706
/gene="SEMA4G"
/replace="gttg"
/replace="gttgcacccactgatggctcggcccgttg"
/db_xref="dbSNP:1850997601"
variation 1679
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:753167511"
variation 1682
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:979985262"
variation 1684
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1221818105"
variation 1685
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1371460605"
variation 1686..1689
/gene="SEMA4G"
/replace=""
/replace="cact"
/db_xref="dbSNP:1422220691"
variation 1687
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:758828192"
variation 1688
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:778460071"
variation 1695
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850998242"
variation 1696
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1170412118"
variation 1697
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1330018610"
variation 1698
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:199635372"
variation 1701
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:779575501"
variation 1702
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:565104337"
variation 1703
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:201564489"
variation 1704
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1400651750"
variation 1705
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850999005"
variation 1706
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:778525725"
variation 1708
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:748004748"
variation 1709
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1213885536"
variation 1715
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:149116714"
variation 1716
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:371636173"
variation 1721
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:367801117"
variation 1722
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:770950663"
variation 1723
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1589990995"
variation 1726
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:889294061"
variation 1732
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1182151325"
variation 1736
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:776709167"
variation 1739
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:759518723"
variation 1740
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:76584327"
variation 1743
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:143118773"
variation 1745
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1186433901"
variation 1748
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:150071842"
variation 1749
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:764503702"
variation 1754
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851000938"
variation 1756
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1345529789"
variation 1757
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:752037569"
variation 1758
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133884735"
variation 1760
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851001443"
variation 1762
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:757714467"
variation 1764
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:779441290"
variation 1765
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1316183503"
variation 1774
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851001826"
variation 1776
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851001929"
variation 1777..1782
/gene="SEMA4G"
/replace="cac"
/replace="caccac"
/db_xref="dbSNP:755502387"
variation 1782
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:147741050"
variation 1783
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851002277"
variation 1795
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:199671205"
variation 1797
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:553260640"
variation 1799
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:1851002597"
variation 1800
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:747781429"
variation 1805
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1231751585"
variation 1806
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1457264028"
variation 1807
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1564797032"
variation 1808
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851003219"
variation 1810
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133884897"
variation 1813
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564797037"
variation 1814
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:771880296"
variation 1816
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851003533"
variation 1820
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1354200251"
exon 1824..1939
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 1824
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851018889"
variation 1825
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:750865022"
variation 1830
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:754532026"
variation 1835
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1302211133"
variation 1837
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1564797210"
variation 1840
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1458448137"
variation 1842
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:201540929"
variation 1843
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:752382102"
variation 1846
/gene="SEMA4G"
/replace="c"
/replace="cctac"
/db_xref="dbSNP:1851020664"
variation 1846
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:7901675"
variation 1847
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:144844358"
variation 1851
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1427873810"
variation 1852
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:542169408"
variation 1853
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:781235374"
variation 1855
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:200666280"
variation 1856
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1400944443"
variation 1857
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1425740385"
variation 1860
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564797257"
variation 1863
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:770024953"
variation 1864
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:775644707"
variation 1867
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:147919269"
variation 1868
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851022799"
variation 1870
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1735148329"
variation 1875
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:372822376"
variation 1878
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:962692236"
variation 1882
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:377379944"
variation 1885
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133886261"
variation 1886
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851023312"
variation 1887
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:762280561"
variation 1890
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1009845265"
variation 1891
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851023747"
variation 1894
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:767751429"
variation 1895
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1384559788"
variation 1897
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:773734788"
variation 1900
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1340727081"
variation 1901
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133886347"
variation 1903
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1661076286"
variation 1904
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1253166327"
variation 1906
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1197875859"
variation 1907
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:761134082"
variation 1909..1912
/gene="SEMA4G"
/replace="tg"
/replace="tgtg"
/db_xref="dbSNP:1851024692"
variation 1910
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1437655804"
variation 1911
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:764733748"
variation 1912
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:752147128"
variation 1923
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:757896884"
variation 1925
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1307458129"
variation 1926..1932
/gene="SEMA4G"
/replace="tctct"
/replace="tctctct"
/db_xref="dbSNP:1187347525"
variation 1926
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1424188963"
variation 1933
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:763844803"
variation 1934
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:377270509"
variation 1939
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1395507326"
exon 1940..2115
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 1941
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:200163492"
variation 1942
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:773503586"
variation 1943
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1316773436"
variation 1945
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:761187011"
variation 1949
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1235416443"
variation 1951
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1306051543"
variation 1954
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:766932360"
variation 1955
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1353345900"
variation 1956
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:777088467"
variation 1958
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1191733049"
variation 1959
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1261588998"
variation 1961
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:762570919"
variation 1962
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1203475590"
variation 1964
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:763459869"
variation 1966
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:141233234"
variation 1967
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:778175945"
variation 1970
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851035626"
variation 1973
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:113498503"
variation 1975
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1453643880"
variation 1978
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133887370"
variation 1983
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:755967370"
variation 1986
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1367220882"
variation 1987
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:200695967"
variation 1990
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851036004"
variation 1996
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1365187139"
variation 1997
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1450944219"
variation 1998
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:962865221"
variation 2000
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:780182850"
variation 2001
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:147992447"
variation 2002
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1453337360"
variation 2006
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:140692272"
variation 2007
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:778822733"
variation 2009
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133887521"
variation 2015
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851036845"
variation 2019
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1328594140"
variation 2020
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1564797582"
variation 2025
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1442804873"
variation 2027
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:748411182"
variation 2028
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851037376"
variation 2031
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851037479"
variation 2033
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:772130257"
variation 2034
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1307898484"
variation 2039
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1449228698"
variation 2041
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:770900988"
variation 2043
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851038019"
variation 2044
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1318990634"
variation 2046
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1236915123"
variation 2049
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1260199125"
variation 2051
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851038517"
variation 2052
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851038668"
variation 2053
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:777961396"
variation 2055
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:747411614"
variation 2056
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1251127577"
variation 2057
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1382570602"
variation 2059
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:771261070"
variation 2060
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:371386076"
variation 2064
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:756576170"
variation 2065
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:759917226"
variation 2067
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:768215640"
variation 2069
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1180693559"
variation 2070
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1417942007"
variation 2074
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:780011724"
variation 2075
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:761371562"
variation 2077
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133887829"
variation 2078
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1392930732"
variation 2081
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851041113"
variation 2082
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1461216948"
variation 2088
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:767343866"
variation 2089
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:750070570"
variation 2090
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1389861288"
variation 2092
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1229597463"
variation 2094
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:760597640"
variation 2095
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:912639818"
variation 2096
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:984794076"
variation 2100
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:766227835"
variation 2104
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:7905266"
variation 2105
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1305237666"
variation 2107..2109
/gene="SEMA4G"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1851042581"
variation 2107
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:754808483"
variation 2109
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:779066804"
variation 2111
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133888012"
variation 2112
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133888016"
variation 2113
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:925424123"
variation 2115
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:752779759"
exon 2116..2177
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 2116
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851052204"
variation 2119
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:138772734"
variation 2122
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851052415"
variation 2123
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:375633368"
variation 2124
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1358635527"
variation 2125..2141
/gene="SEMA4G"
/replace="ga"
/replace="gatacaggacatagaga"
/db_xref="dbSNP:1435619713"
variation 2127
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1271640141"
variation 2130
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:764114736"
variation 2131
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:995770723"
variation 2136
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851053214"
variation 2137..2144
/gene="SEMA4G"
/replace="agag"
/replace="agagagag"
/db_xref="dbSNP:767881320"
variation 2138
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1325570015"
variation 2140
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:190201835"
variation 2141
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851053643"
variation 2143
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851053737"
variation 2149
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:538842540"
variation 2150
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851053925"
variation 2151
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:757411949"
variation 2155
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133889080"
variation 2159
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:781378063"
variation 2160
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:746282456"
variation 2162
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1231622802"
variation 2163
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1279237287"
variation 2165
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:756467836"
variation 2167
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:369529769"
variation 2170
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851054882"
variation 2172
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:534283434"
exon 2178..4489
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 2178
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1373085610"
variation 2179
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851211935"
variation 2180..2192
/gene="SEMA4G"
/replace="ccaccaccac"
/replace="ccaccaccaccac"
/replace="ccaccaccaccaccac"
/db_xref="dbSNP:145835827"
variation 2180..2181
/gene="SEMA4G"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1554884798"
variation 2182
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1334008977"
variation 2186
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1327563265"
variation 2188
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851212995"
variation 2192..2194
/gene="SEMA4G"
/replace=""
/replace="ctg"
/db_xref="dbSNP:755081302"
variation 2196
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:552270687"
variation 2199
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1341977736"
variation 2200
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1235282106"
variation 2201
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1282755788"
variation 2202
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:754085049"
variation 2207
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1589998314"
variation 2210
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1199969523"
variation 2213
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:760031264"
variation 2214
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:753257306"
variation 2216
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133901396"
variation 2217
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:773478369"
variation 2218
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:778125924"
variation 2223
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:570573396"
variation 2225
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1175068535"
variation 2230
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:755545892"
variation 2233
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:779730408"
variation 2235
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1158667773"
variation 2238
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:748889973"
variation 2239
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1384413039"
variation 2242
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:768472015"
variation 2243
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:761068926"
variation 2246
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1442105033"
variation 2247
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851217451"
variation 2248
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851217575"
variation 2250
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1305846909"
variation 2251
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:183718929"
variation 2252
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1232869244"
variation 2254
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:549851109"
variation 2257
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1245506254"
variation 2258
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1353024006"
variation 2261
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:146245319"
variation 2262
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:760851566"
variation 2263
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851218914"
variation 2264
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851219065"
variation 2266
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:770897727"
variation 2268
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1195301504"
variation 2269
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1264768450"
variation 2272
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:777019767"
variation 2274
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:759761969"
variation 2275
/gene="SEMA4G"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1005161073"
variation 2276
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:201001972"
variation 2280
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1451010139"
variation 2281
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851220823"
variation 2286
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1157499811"
variation 2288
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:776051888"
variation 2289
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851221493"
variation 2290
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1005716850"
variation 2291
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851222036"
variation 2295
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851222273"
variation 2296
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1017136365"
variation 2298
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:763219828"
variation 2299
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:764701072"
variation 2300
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:137971825"
variation 2302
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:755671543"
variation 2304
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851223790"
variation 2305
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851224022"
variation 2306
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1355476316"
variation 2307
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1589998686"
variation 2308..2310
/gene="SEMA4G"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1251708384"
variation 2308
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:977978033"
variation 2309
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:765835066"
variation 2310
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851225605"
variation 2311
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1589998724"
variation 2314
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:753494547"
variation 2315
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1315808916"
variation 2317
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1287605179"
variation 2318
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:149389232"
variation 2319
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:144727154"
variation 2320
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851227514"
variation 2323
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:748043373"
variation 2325
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851228007"
variation 2326
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:148516703"
variation 2327
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:374200198"
variation 2329
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851228915"
variation 2332
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:142773171"
variation 2333
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:147237913"
variation 2341
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851229807"
variation 2342
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:141030743"
variation 2344
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851230304"
variation 2347
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851230541"
variation 2350..2351
/gene="SEMA4G"
/replace=""
/replace="tg"
/db_xref="dbSNP:1851230987"
variation 2350
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851230778"
variation 2351
/gene="SEMA4G"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1851231197"
variation 2353
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:770205655"
variation 2356
/gene="SEMA4G"
/replace=""
/replace="g"
/db_xref="dbSNP:1851231852"
variation 2356
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851231625"
variation 2357..2358
/gene="SEMA4G"
/replace=""
/replace="aa"
/db_xref="dbSNP:1851232419"
variation 2357
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:775542275"
variation 2358
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851232649"
variation 2359
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851232858"
variation 2360
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851233038"
variation 2360
/gene="SEMA4G"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1851233269"
variation 2362
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851233489"
variation 2371
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:755113434"
variation 2372
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:764316566"
variation 2377
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:774952582"
variation 2380
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133902664"
variation 2383
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:762161081"
variation 2385
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1298897763"
variation 2388
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851235035"
variation 2389
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:765887043"
variation 2390
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:753406520"
variation 2391
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1408024389"
variation 2395
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851235974"
variation 2398
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:754482102"
variation 2399
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1307475986"
variation 2401
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:764912089"
variation 2402
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:539263557"
variation 2403
/gene="SEMA4G"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1851237219"
variation 2405
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:866091256"
variation 2406
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:558586100"
variation 2407
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:777395006"
variation 2408
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1589998968"
variation 2409
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851238350"
variation 2410
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851238569"
variation 2411
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1049622681"
variation 2412
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:746976668"
variation 2413
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:940882437"
variation 2419
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:757318232"
variation 2422
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851239938"
variation 2424
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851240164"
variation 2425
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1444392472"
variation 2427
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1204049997"
variation 2428
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851240875"
variation 2431
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:977211113"
variation 2433
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851241278"
variation 2434
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1257594428"
variation 2437
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1486401615"
variation 2438
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:781268916"
variation 2439
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:144879682"
variation 2440
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1423563944"
variation 2441
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851242706"
variation 2444
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1171588564"
variation 2446..2448
/gene="SEMA4G"
/replace="cac"
/replace="cacac"
/db_xref="dbSNP:1392472908"
variation 2449
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851243412"
variation 2453
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:902133075"
variation 2455
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851243897"
variation 2457
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851244159"
variation 2459
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851244380"
variation 2465
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851244630"
variation 2468
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1168271228"
variation 2469
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1376084022"
variation 2471
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1416703361"
variation 2474
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:775801456"
variation 2480
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1378378322"
variation 2481
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:997799025"
variation 2482
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851245990"
variation 2485
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:749431067"
variation 2486
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1339881664"
variation 2490
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1031887205"
variation 2492
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:769068051"
variation 2494
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1589999247"
variation 2495
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:774521972"
variation 2496
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1207455851"
variation 2497
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:762152467"
variation 2498
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:772635727"
variation 2499
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851247954"
variation 2500..2504
/gene="SEMA4G"
/replace="tg"
/replace="tgatg"
/db_xref="dbSNP:1187659489"
variation 2500
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851248197"
variation 2501
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851248500"
variation 2503
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851248659"
variation 2504
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:957195278"
variation 2509
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1589999321"
variation 2510
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851249179"
variation 2511
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:759100020"
variation 2512
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1448113201"
variation 2513
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851249681"
variation 2514
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:990022918"
variation 2516
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1395953506"
variation 2517
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:544195173"
variation 2518
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851250291"
variation 2520
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:752430522"
variation 2522
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1358691563"
variation 2527
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1224493460"
variation 2531
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1454241106"
variation 2532
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1265325492"
variation 2533..2537
/gene="SEMA4G"
/replace="c"
/replace="cgcgc"
/db_xref="dbSNP:1851251239"
variation 2533
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:147942823"
variation 2534
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:140546736"
variation 2535
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:751374543"
variation 2536..2537
/gene="SEMA4G"
/replace=""
/replace="tata"
/db_xref="dbSNP:1851251846"
variation 2536
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:757083877"
variation 2539
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1589999484"
variation 2540
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:149914326"
variation 2541
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:750335846"
variation 2550..2565
/gene="SEMA4G"
/replace="gcctcatcctggcctc"
/replace="gcctcatcctggcctcatcctggcctc"
/db_xref="dbSNP:1851252713"
variation 2550
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1380369416"
variation 2552
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:756293264"
variation 2554
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:779930213"
variation 2558
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851253195"
variation 2562
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:939406010"
variation 2563
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:749539011"
variation 2564
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1270578063"
variation 2565
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:71488078"
variation 2566
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851254045"
variation 2568
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:768819125"
variation 2570
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:144937502"
variation 2574..2576
/gene="SEMA4G"
/replace=""
/replace="tct"
/db_xref="dbSNP:569204913"
variation 2577
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:748554644"
variation 2578
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851254882"
variation 2579
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1210510722"
variation 2582
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:887229636"
variation 2583
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:772406976"
variation 2584
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851255424"
variation 2590
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851255543"
variation 2591
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:773734595"
variation 2592
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:761134134"
variation 2595
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851256014"
variation 2597
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:769355889"
variation 2598
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:774916385"
variation 2603
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:542184127"
variation 2604
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1326312908"
variation 2605
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851256871"
variation 2607
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:763691852"
variation 2608
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851257157"
variation 2609
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:149052530"
variation 2610
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:41291464"
variation 2611
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851257680"
variation 2612
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1242957860"
variation 2613
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:527848892"
variation 2614
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851258036"
variation 2615
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:756057332"
variation 2616
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:780027867"
variation 2617
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851258594"
variation 2619
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413539150"
variation 2621
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:200288019"
variation 2622..2628
/gene="SEMA4G"
/replace="act"
/replace="actcact"
/db_xref="dbSNP:748396129"
variation 2622
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1327673019"
variation 2625
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1208690414"
variation 2626
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851259631"
variation 2627
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1274190195"
variation 2629
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133904692"
variation 2630
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1159862173"
variation 2633
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:138505815"
variation 2634
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:140405167"
variation 2638
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851260166"
variation 2639
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1473694674"
variation 2642
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:779055594"
variation 2643
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:531476226"
variation 2645
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1286873399"
variation 2647
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:778047878"
variation 2649
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:145555722"
variation 2650..2675
/gene="SEMA4G"
/replace="ag"
/replace="aggatctgcggtgcaactgcagacag"
/db_xref="dbSNP:1351574365"
variation 2650
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1472206434"
variation 2651
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:771404491"
variation 2652
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415680566"
variation 2653
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851262875"
variation 2654
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851263063"
variation 2656
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851263236"
variation 2658
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:777161655"
variation 2659
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:138067900"
variation 2660
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1282725183"
variation 2662
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1354773723"
variation 2663
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1411329720"
variation 2665
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851264505"
variation 2667
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1305609497"
variation 2668
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851264866"
variation 2672..2674
/gene="SEMA4G"
/replace="a"
/replace="aca"
/db_xref="dbSNP:1349407594"
variation 2673
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1228303776"
variation 2674
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851265432"
variation 2675
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1285314078"
variation 2681
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1358827837"
variation 2688
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1226997498"
variation 2691
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:375760083"
variation 2694
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1438587910"
variation 2696
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:774176474"
variation 2698
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1249714433"
variation 2699
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:761489347"
variation 2700
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1188499233"
variation 2702..2721
/gene="SEMA4G"
/replace="gatgagggtgatgatgaggg"
/replace="gatgagggtgatgatgagggtgatgatgaggg"
/db_xref="dbSNP:772358119"
variation 2704
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:767433560"
variation 2705..2708
/gene="SEMA4G"
/replace="g"
/replace="gagg"
/db_xref="dbSNP:1851267553"
variation 2707
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:773199318"
variation 2708
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:760515196"
variation 2709
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1359315768"
variation 2715
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:145330425"
variation 2717
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:753794838"
variation 2717
/gene="SEMA4G"
/replace="g"
/replace="gg"
/replace="gggg"
/db_xref="dbSNP:1851268481"
variation 2718
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133905431"
variation 2719..2730
/gene="SEMA4G"
/replace="gggggctggggg"
/replace="gggggctggggggctggggg"
/db_xref="dbSNP:1406962803"
variation 2719..2723
/gene="SEMA4G"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1411362753"
variation 2719..2720
/gene="SEMA4G"
/replace=""
/replace="aa"
/db_xref="dbSNP:1851269415"
variation 2719
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:755038247"
variation 2721
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1369335681"
variation 2722
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1414869947"
variation 2723
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851270194"
variation 2724..2735
/gene="SEMA4G"
/replace="ctgggggcctgg"
/replace="ctgggggcctgggggcctgg"
/db_xref="dbSNP:1475018399"
variation 2724
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1335400856"
variation 2725
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590000321"
variation 2727
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1342807731"
variation 2730
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:565974154"
variation 2731
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590000368"
variation 2733
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1283942354"
variation 2737
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:927913032"
variation 2738
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851271928"
variation 2739
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1230873584"
variation 2740
/gene="SEMA4G"
/replace=""
/replace="c"
/db_xref="dbSNP:1487389551"
variation 2740
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851272264"
variation 2741
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851272553"
variation 2742
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1272774402"
variation 2744
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:752924036"
variation 2745
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1201126917"
variation 2746
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851273137"
variation 2749
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:539199769"
variation 2751
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:889434035"
variation 2753
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851273660"
variation 2758
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1011010207"
variation 2761
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851273972"
variation 2767
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851274114"
variation 2770
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:200801941"
variation 2771..2772
/gene="SEMA4G"
/replace=""
/replace="gc"
/replace="gccc"
/replace="gcccc"
/replace="gccccc"
/replace="gcccccc"
/replace="gccccccc"
/db_xref="dbSNP:rs1851274585"
variation 2771
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851274273"
variation 2771
/gene="SEMA4G"
/replace="g"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1554885050"
variation 2772..2776
/gene="SEMA4G"
/replace=""
/replace="cccca"
/db_xref="dbSNP:1851275324"
variation 2772..2775
/gene="SEMA4G"
/replace="ccc"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1307646381"
variation 2772
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1564800318"
variation 2773..2780
/gene="SEMA4G"
/replace="ccc"
/replace="cccagccc"
/db_xref="dbSNP:1451113011"
variation 2773
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1490149544"
variation 2774
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1319007353"
variation 2776..2777
/gene="SEMA4G"
/replace=""
/replace="ag"
/db_xref="dbSNP:1244403035"
variation 2776
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:747411482"
variation 2777
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:757616280"
variation 2777
/gene="SEMA4G"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1851276615"
variation 2778..2793
/gene="SEMA4G"
/replace="ccccacc"
/replace="ccccaccacccccacc"
/db_xref="dbSNP:1851277127"
variation 2778..2781
/gene="SEMA4G"
/replace="cccc"
/replace="ccccccccccc"
/replace="ccccccccccccccc"
/db_xref="dbSNP:1564800345"
variation 2778
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1389197846"
variation 2779
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1434747606"
variation 2781..2786
/gene="SEMA4G"
/replace="c"
/replace="caccac"
/db_xref="dbSNP:1173800017"
variation 2781
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133906339"
variation 2782..2785
/gene="SEMA4G"
/replace=""
/replace="acca"
/db_xref="dbSNP:1399486489"
variation 2782
/gene="SEMA4G"
/replace=""
/replace="a"
/db_xref="dbSNP:1851277715"
variation 2782
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1326270062"
variation 2783
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:781570245"
variation 2784
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:746344453"
variation 2785
/gene="SEMA4G"
/replace=""
/replace="a"
/db_xref="dbSNP:1851278531"
variation 2785
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1438563345"
variation 2786..2805
/gene="SEMA4G"
/replace="cccccaccgcc"
/replace="cccccaccgcccccaccgcc"
/replace="cccccaccgcccccaccgcccccaccgcc"
/db_xref="dbSNP:773176617"
variation 2786..2790
/gene="SEMA4G"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:746736051"
variation 2787
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1334155427"
variation 2788
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:570600855"
variation 2791
/gene="SEMA4G"
/replace=""
/replace="a"
/db_xref="dbSNP:1366311394"
variation 2791
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1437736186"
variation 2792
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1465984153"
variation 2793
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:537981098"
variation 2794
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1364699879"
variation 2796
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1234288227"
variation 2798
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590000861"
variation 2800
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1257825267"
variation 2801
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1476929728"
variation 2802
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:773939741"
variation 2803
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1199749295"
variation 2806
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1268693928"
variation 2807
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:771918484"
variation 2808
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:772968534"
variation 2809
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:368791581"
variation 2810
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1454424276"
variation 2812
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133906812"
variation 2813
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1200638891"
variation 2815
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:766151814"
variation 2819
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:983229924"
variation 2820
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:776467523"
variation 2823
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:908616884"
variation 2824
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:759454826"
variation 2827
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:765317734"
variation 2828
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851283080"
variation 2829
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:941479176"
variation 2830
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:752836080"
variation 2831
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1318914837"
variation 2832
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1590001080"
variation 2839
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:764345648"
variation 2840
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851284021"
variation 2842
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1387547863"
variation 2845
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1303695342"
variation 2846
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:556496771"
variation 2847
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:757591403"
variation 2852
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:574711696"
variation 2853
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1331107517"
variation 2854
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851285121"
variation 2855
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1590001162"
variation 2856
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:781551217"
variation 2857
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1220506232"
variation 2858
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1590001187"
variation 2859
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1407498903"
variation 2863
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:746374262"
variation 2869
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851286122"
variation 2871
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:756701345"
variation 2872
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1211209380"
variation 2874
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851286938"
variation 2880
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:780702310"
variation 2881
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851287302"
variation 2886
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:747701115"
variation 2887
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:771687718"
variation 2890
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1413580384"
variation 2891
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:962140588"
variation 2892
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:976145243"
variation 2898
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:777592361"
variation 2899
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1157657574"
variation 2903
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1402208941"
variation 2905
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851288279"
variation 2906
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1411611036"
variation 2907
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1460684927"
variation 2909
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851288704"
variation 2910
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851288842"
variation 2913
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:921452117"
variation 2914
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851289124"
variation 2915
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1590001329"
variation 2920
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:376187099"
variation 2922
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1295465666"
variation 2926
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:776432076"
variation 2927
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1386472605"
variation 2929
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:141726768"
variation 2930
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:769758760"
variation 2933
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:554126222"
variation 2935
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851290572"
variation 2938
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851290768"
variation 2942
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:199549347"
variation 2943
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:764116745"
variation 2947
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:986379770"
variation 2951
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1246763144"
variation 2953
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1227060568"
variation 2956
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851291821"
variation 2957
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1177109703"
variation 2958
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1263267741"
variation 2964
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851292306"
variation 2965
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:751732798"
variation 2966
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1287154805"
variation 2967
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:150436471"
variation 2968
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:750866450"
variation 2969
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851292761"
variation 2974
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:756516259"
variation 2975
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:375024485"
variation 2977
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851293256"
variation 2978
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1250475715"
variation 2980
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1424709004"
variation 2981
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:754349112"
variation 2983
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851293867"
variation 2984
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1367130443"
variation 2985
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1424259786"
variation 2986
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:369095063"
variation 2987
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1372422706"
variation 2988
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1222819487"
variation 2990
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1590001608"
variation 2992
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:138231164"
variation 2994
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1052793166"
variation 2995
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1307300351"
variation 2996..3003
/gene="SEMA4G"
/replace="tctg"
/replace="tctgtctg"
/db_xref="dbSNP:1851296377"
variation 2998
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:149579572"
variation 2998
/gene="SEMA4G"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1056241246"
variation 3003
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851297087"
variation 3005
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1012519597"
variation 3006
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851297556"
variation 3008
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851297775"
variation 3009
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:770679319"
variation 3013
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851298209"
variation 3014..3015
/gene="SEMA4G"
/replace=""
/replace="g"
/db_xref="dbSNP:1851298451"
variation 3020
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:780708778"
variation 3021
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1011343221"
variation 3025
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:745721149"
variation 3026
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1276335802"
variation 3029
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:769527048"
variation 3030
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851299997"
variation 3034
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:879129411"
variation 3036
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1373716210"
variation 3037
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:775434918"
variation 3038
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:762807711"
variation 3044
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1483848011"
variation 3047
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:768734270"
variation 3054
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851301714"
variation 3057
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1173041083"
variation 3060
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:969880106"
variation 3061
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1003167771"
variation 3070
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1180250824"
variation 3072
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1257290025"
variation 3081
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851302969"
variation 3084..3086
/gene="SEMA4G"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1183256014"
variation 3086
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1482030451"
variation 3088..3090
/gene="SEMA4G"
/replace="ccc"
/replace="ccccc"
/db_xref="dbSNP:1256227888"
variation 3088
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133908720"
variation 3089
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1023540260"
variation 3096
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851304104"
variation 3099
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1436403588"
variation 3100
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:887726997"
variation 3102
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133908809"
variation 3103
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851304584"
variation 3104
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:781204292"
variation 3107
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851305040"
variation 3109
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1014839064"
variation 3112
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851305511"
variation 3113
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:962032640"
variation 3127
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:976114197"
variation 3129
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:745690393"
variation 3132
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851306652"
variation 3133
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851306867"
variation 3134
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851307077"
variation 3143
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851307315"
variation 3148
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:950718210"
variation 3150..3151
/gene="SEMA4G"
/replace=""
/replace="ag"
/db_xref="dbSNP:1590001957"
variation 3153..3178
/gene="SEMA4G"
/replace=""
/replace="caggcccagccaaagccccctcctca"
/db_xref="dbSNP:1590001967"
variation 3155
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851308106"
variation 3156
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851308337"
variation 3157
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:953557741"
variation 3158
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1362537886"
variation 3162
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:986736713"
variation 3166
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:982791219"
variation 3168..3172
/gene="SEMA4G"
/replace="ccccc"
/replace="cccccc"
/db_xref="dbSNP:1851309403"
variation 3169
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1410299026"
variation 3174
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:908564430"
variation 3177..3178
/gene="SEMA4G"
/replace=""
/replace="ca"
/db_xref="dbSNP:2133909252"
variation 3180
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:962745699"
variation 3181
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1453609825"
variation 3183
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:974131731"
variation 3184
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:921398275"
variation 3185
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851310611"
variation 3186
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1308719600"
variation 3190
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133909360"
variation 3193
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1564800882"
variation 3197
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851311037"
variation 3199
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1416775905"
variation 3201
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851311226"
variation 3202
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1193893340"
variation 3204
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:932827701"
variation 3207
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1385143611"
variation 3209
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:947584470"
variation 3211
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:977712151"
variation 3213
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1242406016"
variation 3214
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851312352"
variation 3215
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1333845024"
variation 3216
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:564705467"
variation 3217
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:912794871"
variation 3218
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1342470994"
variation 3220
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1331866472"
variation 3225
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851313372"
variation 3235
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851313579"
variation 3239
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1316233169"
variation 3240..3242
/gene="SEMA4G"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1382183614"
variation 3245
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851314310"
variation 3246
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:531413037"
variation 3252
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1460240665"
variation 3254..3261
/gene="SEMA4G"
/replace="tgc"
/replace="tgccctgc"
/db_xref="dbSNP:1236997858"
variation 3255
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1171020858"
variation 3256
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851315304"
variation 3258
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1478564784"
variation 3260
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:757063742"
variation 3262
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1191784859"
variation 3264
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1433241980"
variation 3266
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851316321"
variation 3269
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1269427005"
variation 3285..3294
/gene="SEMA4G"
/replace="cctaa"
/replace="cctaacctaa"
/db_xref="dbSNP:1342086795"
variation 3288
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:543028700"
variation 3291
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851317105"
variation 3297
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2295717"
variation 3302
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:781060343"
variation 3306
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851317720"
variation 3307
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:561836841"
variation 3308
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851318174"
variation 3311
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:745805497"
variation 3312
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:947905136"
variation 3314..3315
/gene="SEMA4G"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1242415993"
variation 3314
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851318713"
variation 3315
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:774547564"
variation 3317
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1304136053"
variation 3319..3327
/gene="SEMA4G"
/replace="c"
/replace="ctcctgttc"
/db_xref="dbSNP:1439323352"
variation 3319
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1394221728"
variation 3323
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1332383377"
variation 3326
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851319701"
variation 3327
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:887621111"
variation 3328
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1006521433"
variation 3330
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2295716"
variation 3331
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1035962765"
variation 3337..3338
/gene="SEMA4G"
/replace="gc"
/replace="gcgc"
/db_xref="dbSNP:374469923"
variation 3339
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:767847442"
variation 3344
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1165781151"
variation 3345
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:547371500"
variation 3346..3351
/gene="SEMA4G"
/replace="ct"
/replace="ctttct"
/db_xref="dbSNP:1564801033"
variation 3347..3349
/gene="SEMA4G"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1851321381"
variation 3353
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590002545"
variation 3357
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851321658"
variation 3361
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851321816"
variation 3362
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1427851024"
variation 3363
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1169802472"
variation 3366
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133910482"
variation 3368
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1358850075"
variation 3372
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:761133475"
variation 3373
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1191685942"
variation 3374
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851322719"
variation 3376
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:565832622"
variation 3377
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1301023166"
variation 3379
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1238599331"
variation 3380
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:140873008"
variation 3381..3384
/gene="SEMA4G"
/replace="atat"
/replace="atatat"
/db_xref="dbSNP:1180219371"
variation 3382
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:775161961"
variation 3383
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851323614"
variation 3385
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1435583593"
variation 3386
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1347264509"
variation 3392
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:755490675"
variation 3393
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1022174562"
variation 3394
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851324366"
variation 3396
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1282490941"
variation 3405
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1232746478"
variation 3407
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851325083"
variation 3413..3415
/gene="SEMA4G"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1564801111"
variation 3413
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1015510000"
variation 3416
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:551143626"
variation 3418
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1309192746"
variation 3419
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1446522565"
variation 3420
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851326399"
variation 3422
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1313501848"
variation 3424
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851326936"
variation 3425
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851327156"
variation 3427
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1381487456"
variation 3433
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1370845164"
variation 3442
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1212785459"
variation 3443
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:962694375"
variation 3444
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851328377"
variation 3447
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:11591349"
variation 3448
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:536866327"
variation 3449
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1250348904"
variation 3453
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1447859281"
variation 3454
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1186203566"
variation 3455
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:977649336"
variation 3458
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133911153"
variation 3462
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:756712868"
variation 3465
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1204147027"
variation 3466
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:556345883"
variation 3467
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1434047317"
variation 3469
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851330601"
variation 3471
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1173815254"
variation 3472
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:567995095"
variation 3473
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:986972740"
variation 3476
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1322261528"
variation 3482
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1386272160"
variation 3483
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1468467340"
variation 3484
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851331669"
variation 3485
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:745459702"
variation 3487
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:755937099"
variation 3488
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851332127"
variation 3491
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242453332"
variation 3492
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:11190780"
variation 3493
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1369013608"
variation 3497
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1217004954"
variation 3499
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:749061715"
variation 3507
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1323427412"
variation 3508
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:768679541"
variation 3509
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:562213978"
variation 3512
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1463832678"
variation 3513
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1215245125"
variation 3515
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1392099800"
variation 3518
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1247539943"
variation 3519
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851334603"
variation 3521
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1489476783"
variation 3522
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851335052"
variation 3527
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:774150942"
variation 3528
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1330576370"
variation 3529
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:554180516"
variation 3530
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1161357971"
variation 3531
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1222920929"
variation 3536..3540
/gene="SEMA4G"
/replace="ct"
/replace="cttct"
/db_xref="dbSNP:1409419478"
variation 3539..3543
/gene="SEMA4G"
/replace="ct"
/replace="ctcct"
/db_xref="dbSNP:1399901647"
variation 3544
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851337089"
variation 3545
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1164988814"
variation 3547
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1347204536"
variation 3550..3554
/gene="SEMA4G"
/replace="tt"
/replace="ttctt"
/db_xref="dbSNP:1851337943"
variation 3552
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1351283007"
variation 3554
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851338509"
variation 3560
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:748317224"
variation 3563
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1301958846"
variation 3567
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851339309"
variation 3572
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1350650732"
variation 3573
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:771987099"
variation 3574
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:909015462"
variation 3575
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:947024954"
variation 3577
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1348931588"
variation 3593
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1044109678"
variation 3594
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851341027"
variation 3602
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851341287"
variation 3606
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851341554"
variation 3608
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1223598937"
variation 3611
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:941896553"
variation 3617
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1590003340"
variation 3618..3621
/gene="SEMA4G"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:749161619"
variation 3618
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:867056759"
variation 3620
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851342959"
variation 3621
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1341846221"
variation 3625
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1323698735"
variation 3628
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1219725456"
variation 3629
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:897779980"
variation 3630
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1483432059"
variation 3632
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:766759551"
variation 3633
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133912160"
variation 3635
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1398820091"
variation 3638
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:938445182"
variation 3639
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1249568875"
variation 3641..3643
/gene="SEMA4G"
/replace="t"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:1564801421"
variation 3649
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851345504"
variation 3651
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851345730"
variation 3653
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133912278"
variation 3655..3657
/gene="SEMA4G"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:34661749"
variation 3655
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1469396700"
variation 3657
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1590003500"
variation 3660
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1051674712"
variation 3661
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1473643656"
variation 3662
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415748001"
variation 3668
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1403242646"
variation 3670
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851347694"
variation 3671
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851347910"
variation 3672
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413115744"
variation 3676
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1186071819"
variation 3677
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1162547813"
variation 3678
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1370560535"
variation 3684
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:889128459"
variation 3685
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851348837"
variation 3686
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1431132181"
variation 3691..3699
/gene="SEMA4G"
/replace="ctcc"
/replace="ctcccctcc"
/db_xref="dbSNP:1310336433"
variation 3693
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851349496"
variation 3694
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1056944101"
variation 3697
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851350086"
variation 3699
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:886274992"
variation 3701
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1828080527"
variation 3704..3710
/gene="SEMA4G"
/replace="cct"
/replace="ccttcct"
/db_xref="dbSNP:1442168150"
variation 3704
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1285150909"
variation 3705
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:150176473"
variation 3708
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1284040676"
variation 3713
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1243979563"
variation 3715
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1454985511"
variation 3719
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1016127185"
variation 3720
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1342914307"
variation 3721
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1207413139"
variation 3724
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1272637340"
variation 3726..3731
/gene="SEMA4G"
/replace=""
/replace="atcagc"
/db_xref="dbSNP:1437134295"
variation 3726
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:546548368"
variation 3729..3738
/gene="SEMA4G"
/replace=""
/replace="agcctcccca"
/db_xref="dbSNP:1232285107"
variation 3732
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851353656"
variation 3733
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851353903"
variation 3734..3737
/gene="SEMA4G"
/replace="ccc"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1851354331"
variation 3734
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:999055334"
variation 3735..3739
/gene="SEMA4G"
/replace="c"
/replace="cccac"
/db_xref="dbSNP:1188248769"
variation 3736
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:558511473"
variation 3738
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851355064"
variation 3739
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1471688492"
variation 3740..3741
/gene="SEMA4G"
/replace=""
/replace="gtgtga"
/db_xref="dbSNP:1279740182"
variation 3740
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564801584"
variation 3741
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1182551535"
variation 3747
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1390425592"
variation 3748
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:866465441"
variation 3750
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:899127927"
variation 3751
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851356441"
variation 3757..3758
/gene="SEMA4G"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1851356699"
variation 3762..3764
/gene="SEMA4G"
/replace="t"
/replace="tat"
/db_xref="dbSNP:776469814"
variation 3762
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:1564801613"
variation 3763
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:995448141"
variation 3764
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1406943937"
variation 3765..3770
/gene="SEMA4G"
/replace="gaga"
/replace="gagaga"
/db_xref="dbSNP:1031921038"
variation 3766
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1352660512"
variation 3767
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1166136937"
variation 3769
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:960318556"
variation 3773
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851358185"
variation 3778
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1217254719"
variation 3781
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:993082702"
variation 3782
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851358464"
variation 3783
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851358683"
variation 3785
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:576676078"
variation 3786
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851359112"
variation 3788
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:954125817"
variation 3789
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1409881469"
variation 3794
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1590004029"
variation 3795
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1335465291"
variation 3796
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1361197103"
variation 3798
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1450956457"
variation 3804
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1314573273"
variation 3805
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242083934"
variation 3807..3808
/gene="SEMA4G"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1366179476"
variation 3807
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851361189"
variation 3809
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1734059355"
variation 3810..3813
/gene="SEMA4G"
/replace="aaca"
/replace="aacaaca"
/db_xref="dbSNP:398114688"
variation 3811..3818
/gene="SEMA4G"
/replace="acac"
/replace="acacacac"
/db_xref="dbSNP:146737296"
variation 3811
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851362081"
variation 3813
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1470152414"
variation 3814
/gene="SEMA4G"
/replace=""
/replace="c"
/db_xref="dbSNP:1554885387"
variation 3816..3819
/gene="SEMA4G"
/replace="c"
/replace="cacc"
/db_xref="dbSNP:1564801730"
variation 3816
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:980911684"
variation 3824
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:908989869"
variation 3825
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1318120156"
variation 3828
/gene="SEMA4G"
/replace=""
/replace="a"
/db_xref="dbSNP:1851363694"
variation 3829
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1297128475"
variation 3830..3831
/gene="SEMA4G"
/replace=""
/replace="at"
/db_xref="dbSNP:201653131"
variation 3831
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851363979"
variation 3832
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:941859324"
variation 3834
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1275426272"
variation 3840
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:544003449"
variation 3847
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:561580399"
variation 3852
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:987306998"
variation 3853
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1761267634"
variation 3859
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851365080"
variation 3860
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:760046546"
variation 3863
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851365638"
variation 3871
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:570837619"
variation 3873
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851366097"
variation 3874
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1461145737"
variation 3875
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:956410819"
variation 3879
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1172757131"
variation 3880
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590004294"
variation 3884
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:765696472"
variation 3885..3892
/gene="SEMA4G"
/replace="ctgt"
/replace="ctgtctgt"
/db_xref="dbSNP:1851367609"
variation 3885
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851367435"
variation 3887
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:776736066"
variation 3899
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:541757083"
variation 3900
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1455911411"
variation 3902
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133914046"
variation 3904
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:947649741"
variation 3905
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:540658889"
variation 3910
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1458477096"
variation 3912
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851368804"
variation 3927
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:979738620"
variation 3928
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133914138"
variation 3929
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1419920691"
variation 3947
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851369510"
variation 3950
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:926970920"
variation 3952
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:938406307"
variation 3959
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1345587818"
variation 3964..3972
/gene="SEMA4G"
/replace="ggatg"
/replace="ggatggatg"
/db_xref="dbSNP:1156991738"
variation 3965
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1590004435"
variation 3970
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1411538590"
variation 3971
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1447292211"
variation 3972
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1057292576"
variation 3982
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1401448436"
variation 3983
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:148889377"
variation 3985
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1354019972"
variation 3988
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1357855929"
variation 3989
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:185501392"
variation 3990
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1437149072"
variation 3991
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1393859490"
variation 3994
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1314077837"
variation 3998..3999
/gene="SEMA4G"
/replace="c"
/replace="cc"
/db_xref="dbSNP:745620184"
variation 4004
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851373532"
variation 4005
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1357883329"
variation 4007
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1058101"
variation 4008..4012
/gene="SEMA4G"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1564801889"
variation 4009
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1043523463"
variation 4011
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1440759734"
variation 4012
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1037520890"
variation 4013
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851374834"
variation 4019
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851375125"
variation 4023
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851375359"
variation 4028..4032
/gene="SEMA4G"
/replace="tc"
/replace="tcctc"
/db_xref="dbSNP:1851375586"
variation 4029
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1287105200"
variation 4030
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:899075093"
variation 4032
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851376270"
variation 4033
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:758453345"
variation 4034
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:999022475"
variation 4036
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:533032857"
variation 4038
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851377123"
variation 4043
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851377286"
variation 4045..4053
/gene="SEMA4G"
/replace="gggaaaggg"
/replace="gggaaagggggaaaggg"
/db_xref="dbSNP:1237569905"
variation 4045
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1276666015"
variation 4051
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851377980"
variation 4052..4058
/gene="SEMA4G"
/replace="ggag"
/replace="ggaggag"
/db_xref="dbSNP:1212458091"
variation 4058
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:539958411"
variation 4064
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1031806643"
variation 4066
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:996061169"
variation 4067..4071
/gene="SEMA4G"
/replace="tgtct"
/replace="tgtctgtct"
/db_xref="dbSNP:1851379088"
variation 4067..4069
/gene="SEMA4G"
/replace="t"
/replace="tgt"
/db_xref="dbSNP:1851378916"
variation 4068
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1276056518"
variation 4069
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1318520975"
variation 4072
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851379758"
variation 4075
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1028300853"
variation 4076
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1222315298"
variation 4081
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:145456828"
variation 4083
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851380461"
variation 4087
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1259577119"
variation 4088
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851380817"
variation 4089
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851380992"
variation 4095
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:969446661"
variation 4099
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851381422"
variation 4103
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1313689869"
variation 4104
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851381840"
variation 4107
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851382067"
variation 4113
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:980495734"
variation 4115
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1016423976"
variation 4117
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851382772"
variation 4121
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:764283941"
variation 4122
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851383229"
variation 4123
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851383454"
variation 4124
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:889784981"
variation 4125
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851383892"
variation 4130
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851384118"
variation 4131
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1482005638"
variation 4132
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1008277694"
variation 4133
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:751801892"
variation 4139
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133915301"
variation 4144
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1590004825"
variation 4147
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851385217"
variation 4148..4149
/gene="SEMA4G"
/replace=""
/replace="ct"
/db_xref="dbSNP:971792769"
variation 4148
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851385462"
variation 4149
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:919060865"
variation 4151
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851386135"
variation 4160
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851386346"
variation 4161
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1365943648"
variation 4162
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1160574437"
variation 4163
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:549901293"
variation 4164
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851387327"
variation 4165
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:987778470"
variation 4167
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:956145941"
variation 4171
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1189614913"
variation 4172
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1484440106"
variation 4176
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851388353"
variation 4177
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851388576"
variation 4178
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:722435"
variation 4180
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851389219"
variation 4181
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133915599"
variation 4183
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1174615834"
variation 4185
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1377821148"
variation 4186
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1486785377"
variation 4188
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851390176"
variation 4190
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851390425"
variation 4191
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1021817552"
variation 4195
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851390914"
variation 4199
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1258766345"
variation 4200
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:13114"
variation 4202
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:530575708"
variation 4209
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1322070191"
variation 4210
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851392002"
variation 4212
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851392246"
variation 4214
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590005004"
variation 4216
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851392702"
variation 4220
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1294208197"
variation 4223
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851393161"
variation 4228
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:796584525"
variation 4229
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851393640"
variation 4232
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1443718900"
variation 4233
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:549209014"
variation 4234..4238
/gene="SEMA4G"
/replace="ccccc"
/replace="cccccc"
/db_xref="dbSNP:1851394245"
variation 4236
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851394479"
variation 4238
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851394644"
variation 4239
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1272765213"
variation 4240
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:535391514"
variation 4243
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133915982"
variation 4247
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:722434"
variation 4248
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:756150215"
variation 4249
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851395747"
variation 4251..4259
/gene="SEMA4G"
/replace="tga"
/replace="tgaggatga"
/db_xref="dbSNP:1851395903"
variation 4254
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1287595742"
variation 4256
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1590005102"
variation 4257..4262
/gene="SEMA4G"
/replace="tg"
/replace="tgactg"
/db_xref="dbSNP:1282127784"
variation 4261..4263
/gene="SEMA4G"
/replace="t"
/replace="tgt"
/db_xref="dbSNP:1851396880"
variation 4262
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851397104"
variation 4265
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851397297"
variation 4266
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851397538"
variation 4271
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851397765"
variation 4275
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1453577215"
variation 4276
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851398062"
variation 4277
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1339982424"
variation 4282
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:992545494"
variation 4283
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1473984676"
variation 4287
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:377579383"
variation 4290
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1193217573"
variation 4294
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1429752865"
variation 4295
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:535979784"
variation 4297
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851399630"
variation 4298
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1053207362"
variation 4305
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1204475752"
variation 4310
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1468760178"
variation 4313
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851400265"
variation 4314
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:895968520"
variation 4321
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:547453410"
variation 4322
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1215821939"
variation 4325
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1014460178"
variation 4327
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851401422"
variation 4330
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1272754894"
variation 4334
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590005244"
variation 4337
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:566052365"
variation 4338
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1228291159"
variation 4339
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:539856889"
variation 4340..4347
/gene="SEMA4G"
/replace="aatg"
/replace="aatgaatg"
/db_xref="dbSNP:1851402794"
variation 4343
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1294126122"
variation 4346
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:1245235656"
variation 4347
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1023629686"
variation 4356
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:907599520"
variation 4357
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851403820"
variation 4358
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1194666457"
variation 4360
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1459569804"
variation 4363
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851404319"
variation 4366
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1397200065"
variation 4369
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1006217092"
variation 4371
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851405001"
variation 4375
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:940472396"
variation 4379
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1370830712"
variation 4380
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851405676"
variation 4383
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851405873"
variation 4385
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851406098"
variation 4388
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564802346"
variation 4391
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1168572915"
variation 4395
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1454629864"
variation 4399
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851406807"
variation 4405
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1015896546"
variation 4406
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1183846917"
variation 4407
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1590005486"
variation 4408..4409
/gene="SEMA4G"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1851407769"
variation 4408
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1037468969"
variation 4409
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1267016453"
variation 4410
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851408064"
variation 4412
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:971763006"
variation 4413
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:780109310"
variation 4423
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851408894"
variation 4426
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:920446283"
variation 4428
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1590005630"
variation 4429..4434
/gene="SEMA4G"
/replace="ggggag"
/replace="ggggagggggag"
/db_xref="dbSNP:1851409933"
variation 4429
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1026045787"
variation 4430
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1249625499"
variation 4434
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1397803701"
variation 4435
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851410880"
variation 4437
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:11190781"
variation 4438
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851411332"
variation 4440
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:375892284"
variation 4447
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590005760"
variation 4449
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851412105"
variation 4450
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:1348958879"
variation 4450
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590005788"
variation 4453
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1441105677"
variation 4454
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:890411724"
variation 4455
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133917246"
variation 4456
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1008640180"
variation 4457
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:576811967"
variation 4458..4459
/gene="SEMA4G"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1851413621"
variation 4459
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:537243928"
variation 4460
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:555966416"
variation 4461
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:573637014"
variation 4463
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:934667679"
variation 4464
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1171676783"
regulatory 4467..4472
/regulatory_class="polyA_signal_sequence"
/gene="SEMA4G"
/note="hexamer: AATAAA"
variation 4475
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:866768376"
variation 4476
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1010346124"
variation 4477
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851414998"
variation 4478
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851415299"
variation 4482
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:917372450"
variation 4483..4486
/gene="SEMA4G"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1439739794"
variation 4484
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590006249"
variation 4486
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851416502"
polyA_site 4489
/gene="SEMA4G"
/note="major polyA site"
ORIGIN
agccgcggccccttcctctcgcagctggtgctgtggggccgcggagccgcgcgtcgctgtctctatggccccggatccgagcgcaaagaaaacggacctcagaaaaccaggactagctctactgtcgggggcagggtgaccccatcagtaacctacaacccctctagaacttcacaactccctctcaccatggagtttgcatttgatgcagaaaggcatgtgatccctccctccttctgacctcttagctggggattccatggccacacaaccctgtgactccatgtccccccgattccaggaccccccatggccccatgattccttgactcctatgaccttatgacccctgaccttccaagtgacttccttggactttgacccctgtgactgtgcttcccattccccgcccccacaacctgtgactctggctccctttgggggtcttgttagtctgggcctccccaggaagatgtgggggaggctctggcccctcctcctcagcatcctcacagcaactgcagtcccaggaccctcactgcggagaccgtctagagaactagatgccacccctcggatgaccataccctatgaagagctctctgggacccggcacttcaagggccaagcccagaactactcaacactgctgctggaggaggcctcagcaaggctgctggtgggagcccgaggtgccctgttctctctcagtgccaacgacataggagatggggctcacaaagagatccactgggaagcctccccagagatgcaaagcaaatgtcatcaaaaagggaaaaacaaccagacggagtgctttaaccatgtgcggttcctgcagcggctcaattctacccacctctatgcatgtgggactcacgccttccagcccctctgtgcagccattgatgctgaggccttcaccttgccaaccagcttcgaggaggggaaggagaagtgtccttatgacccagcccgtggcttcacaggcctcatcattgatggaggcctctacacagccactaggtatgaattccggagcattcctgacatccgccggagccgccacccacactccctgagaactgaggagacaccaatgcattggctcaatgatgcggagtttgtgttctccgtcctcgtgcgggagagcaaggccagtgcagtgggtgatgatgacaaggtgtactacttcttcacggagcgtgccactgaggagggctctggcagcttcactcagagccgcagcagtcaccgtgtggcccgtgtggctcgtgtctgcaagggagacctgggagggaagaagatcctgcagaagaagtggacttccttcctgaaagcccgtctcatctgccacattccactgtatgagacactgcgtggggtctgcagcctggatgctgaaacctcaagccgtacacacttctatgcagccttcacgctgagcacacagtggaagaccctggaggcctcagccatctgccgctatgacctggcagagatccaggctgtctttgcaggaccctatatggaataccaggatggttcccggcgctggggtcgctatgagggtggggtgcctgagccccggcctggctcgtgtatcacagattcattgcgcagccaaggctacaattcatcccaagacttgccatccctggtcctggactttgtaaagttgcacccactgatggctcggcccgttgtgcccacacgtggacggcccctgctgctcaagcgcaacatacgctacacacaccttacagggacacctgtcaccacgcctgctggacctacctatgacctgctctttctgggcacagctgatggctggatccacaaggccgtagtcctgggctctgggatgcacattattgaagagacacaagtgttcagggagtcccagtctgtggaaaatctagtcatctctctattgcagcacagcctctatgtgggggctcctagcggagtcatccagctaccactctccagctgctcccgctaccgatcctgctatgactgcatcttggcccgagacccctactgtggctgggaccctggcacccatgcctgcgcagcagccaccaccatagccaacaggtcccagggaagcaggacagcactgatacaggacatagagagaggaaatcgaggctgtgagagcagcagggatacagggccaccaccaccactgaagacccgctctgtgctccggggtgatgatgtcctcctgccctgtgaccagccatccaacctggcccgggccttgtggctactcaatgggagcatgggcctgagcgatgggcagggtggctaccgtgtgggcgtggacgggctgctggttacagatgcacagcctgagcacagtggcaactatggctgctatgccgaggaaaatggcctccgcaccctgctggcctcctatagtctcacagtccggccagccactcctgccccagctccaaaagcccctgccacacctggggcacagctggcacctgatgtgagactgctctatgtgctagccattgccgcgcttggtggcctctgcctcatcctggcctcctccctcctctatgtggcctgtctgcgggaaggcagacgagggcgccgacggaaatactcactgggtcgggccagccgggcaggaggatctgcggtgcaactgcagacagtctcaggccagtgtcctggagaggaagatgagggtgatgatgagggggctgggggcctggagggcagctgtctccagatcatccctggggagggagccccagccccaccacccccaccgcccccaccgccaccggctgagctgaccaatggcttggtggcactgcccagccggctgcggaggatgaatggcaatagctatgtgcttctgaggcagagcaacaatggagtaccagcagggccctgctccttcgccgaggaactcagccgcatcctggaaaaaaggaagcacacgcagctcgtggagcagctagatgagagctctgtctgagcccagcctcccagaacaaatgctcttccaagccagcctatctgtcccaggctgggccactgcctccctaacacagccaccctcccttcattacccccactccatacccttctcccaactttttgatgtccctgtagggctggccagtcaggcccagccaaagccccctcctcagtctccacagacccacatgtgagcagcccaggcccatcggtgctcctcagaggtaggtgctccctcaggatcaggtgccctgcagacccagagccagttcctatcccctaacctaaacacttataggtgaggactccatcctcctgttccattcatctgcccaaaccctttctctttctcccaggcagggctctgcaggtccatatgggctcaatgtcaccaccctctgcatggccctgtgtgctggatggtcctgaaaccagacaagacctctgccagccacctaagccctgcgtacattcacatgcacacatggaagaatgtttatcggctgggctgcagtgcccccaccctcaccttctcctggtgcattcttgtttcatccctgcttctggacttggggtaccctcccaattgccacatcctatctggtcctcttccccagccccatgtggtgacctctttgtcaagagcttgggaacgggccagcctggggaggtaagactgcatcactcccctcctctcccttcctgtgtggcccttgtgaatcagcctccccactctccttggtcattctcaagagtatgagagacagagctccaggcatgtcccatccccatgcacatgtggtaacacacacctgtatcacacatgtgcttacatttccactcacatgcacctctgagcctcccttgctgtcttggacctgtctgttgggtttagtccgtggacatttcagagggagatccccctcccatttaactgtcctcacaggcccttgcctaggatggatgaccaacactgcactcaatgagccagcctctcttttgggggaatcaagcatttgcttcctctagactacagcagggaaagggaggagaaatctgatgtctcaactggcacatgaagcccattcttggaactatgcaaagggcagaggctgggagtttggacgcttagctcctacccctgtcctacctcaccggggcactttcaggggccaggggcctctgaagtctctaggcctatatgggacaatcaattctgactgagctcccccattcccctcgggtgaggatgactgttatttttgtagctgagaacgtggaatcccacgggtttttactgcccttcacccaacctctcccacctccaccccacaatgaatgtatttattgtgagaatggctacacttctttaggaatgcccccacttacaaccaggtgggtggaacaggcatgtgacagagtggggagcctgggctcagctcctccccctgccgttggttaataaacaccctttttccccaca
//
by
@meso_cacase at
DBCLS
This page is licensed under a
Creative Commons Attribution 4.0 International License (CC BY 4.0).
If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596.
[Full Text]