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Previous release (v1)
2024-05-01 05:12:45, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_001393925 4474 bp mRNA linear PRI 26-JUN-2023
DEFINITION Homo sapiens semaphorin 4G (SEMA4G), transcript variant 3, mRNA.
ACCESSION NM_001393925 XM_024448091
VERSION NM_001393925.1
KEYWORDS RefSeq.
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 4474)
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 4474)
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 4474)
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 4474)
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 4474)
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 4474)
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 4474)
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 4474)
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 XM_024448091.1.
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].
##Evidence-Data-START##
Transcript exon combination :: SRR18074969.477231.1,
SRR14038197.397691.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
SAMEA1968540, SAMEA1968968
[ECO:0000348]
##Evidence-Data-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
1940-2100 AL133215.17 63646-63806
2101-2162 AL133215.17 63992-64053
2163-4474 AL133215.17 66129-68440
FEATURES Location/Qualifiers
source 1..4474
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="10"
/map="10q24.31"
gene 1..4474
/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..2989
/gene="SEMA4G"
/note="isoform 3 precursor is encoded by transcript
variant 3; sema domain, immunoglobulin domain (Ig),
transmembrane domain (TM) and short cytoplasmic domain,
(semaphorin) 4G"
/codon_start=1
/product="semaphorin-4G isoform 3 precursor"
/protein_id="NP_001380854.1"
/db_xref="CCDS:CCDS91320.1"
/db_xref="GeneID:57715"
/db_xref="HGNC:HGNC:10735"
/db_xref="MIM:618991"
/translation="
MWGRLWPLLLSILTATAVPGPSLRRPSRELDATPRMTIPYEELSGTRHFKGQAQNYSTLLLEEASARLLVGARGALFSLSANDIGDGAHKEIHWEASPEMQSKCHQKGKNNQTECFNHVRFLQRLNSTHLYACGTHAFQPLCAAIDAEAFTLPTSFEEGKEKCPYDPARGFTGLIIDGGLYTATRYEFRSIPDIRRSRHPHSLRTEETPMHWLNDAEFVFSVLVRESKASAVGDDDKVYYFFTERATEEGSGSFTQSRSSHRVARVARVCKGDLGGKKILQKKWTSFLKARLICHIPLYETLRGVCSLDAETSSRTHFYAAFTLSTQWKTLEASAICRYDLAEIQAVFAGPYMEYQDGSRRWGRYEGGVPEPRPGSCITDSLRSQGYNSSQDLPSLVLDFVKLHPLMARPVVPTRGRPLLLKRNIRYTHLTGTPVTTPAGPTYDLLFLGTADGWIHKAVVLGSGMHIIEETQVFRESQSVENLVISLLQHSLYVGAPSGVIQLPLSSCSRYRSCYDCILARDPYCGWDPGTHACAAATTIANRTALIQDIERGNRGCESSRDTGPPPPLKTRSVLRGDDVLLPCDQPSNLARALWLLNGSMGLSDGQGGYRVGVDGLLVTDAQPEHSGNYGCYAEENGLRTLLASYSLTVRPATPAPAPKAPATPGAQLAPDVRLLYVLAIAALGGLCLILASSLLYVACLREGRRGRRRKYSLGRASRAGGSAVQLQTVSGQCPGEEDEGDDEGAGGLEGSCLQIIPGEGAPAPPPPPPPPPPAELTNGLVALPSRLRRMNGNSYVLLRQSNNGVPAGPCSFAEELSRILEKRKHTQLVEQLDESSV"
sig_peptide 473..523
/gene="SEMA4G"
/inference="COORDINATES: ab initio prediction:SignalP:4.0"
mat_peptide 524..2986
/gene="SEMA4G"
/product="Semaphorin-4G. /id=PRO_0000032333"
/note="propagated from UniProtKB/Swiss-Prot (Q9NTN9.1)"
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..2143
/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 2171..2422
/gene="SEMA4G"
/note="Immunoglobulin (Ig)-like domain of the class IV
semaphorin Sema4B; Region: Ig_Sema4B_like; cd05872"
/db_xref="CDD:409456"
misc_feature 2171..2191
/gene="SEMA4G"
/note="Ig strand A [structural motif]; Region: Ig strand
A"
/db_xref="CDD:409456"
misc_feature 2201..2227
/gene="SEMA4G"
/note="Ig strand B [structural motif]; Region: Ig strand
B"
/db_xref="CDD:409456"
misc_feature order(2207..2209,2330..2332)
/gene="SEMA4G"
/note="dimer interface [polypeptide binding]; other site"
/db_xref="CDD:409456"
misc_feature 2243..2263
/gene="SEMA4G"
/note="Ig strand C [structural motif]; Region: Ig strand
C"
/db_xref="CDD:409456"
misc_feature 2264..2266
/gene="SEMA4G"
/note="N-linked (GlcNAc...) asparagine.
/evidence=ECO:0000255; propagated from
UniProtKB/Swiss-Prot (Q9NTN9.1); glycosylation site"
misc_feature 2267..2278
/gene="SEMA4G"
/note="Ig strand C' [structural motif]; Region: Ig strand
C'"
/db_xref="CDD:409456"
misc_feature 2297..2311
/gene="SEMA4G"
/note="Ig strand D [structural motif]; Region: Ig strand
D"
/db_xref="CDD:409456"
misc_feature 2315..2338
/gene="SEMA4G"
/note="Ig strand E [structural motif]; Region: Ig strand
E"
/db_xref="CDD:409456"
misc_feature 2354..2383
/gene="SEMA4G"
/note="Ig strand F [structural motif]; Region: Ig strand
F"
/db_xref="CDD:409456"
misc_feature 2498..2560
/gene="SEMA4G"
/note="propagated from UniProtKB/Swiss-Prot (Q9NTN9.1);
transmembrane region"
misc_feature 2639..2803
/gene="SEMA4G"
/note="propagated from UniProtKB/Swiss-Prot (Q9NTN9.1);
Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite"
misc_feature 2855..2857
/gene="SEMA4G"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:23186163; propagated from
UniProtKB/Swiss-Prot (Q9NTN9.1); phosphorylation site"
misc_feature 2981..2983
/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..2100
/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"
exon 2101..2162
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 2101
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851052204"
variation 2104
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:138772734"
variation 2107
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851052415"
variation 2108
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:375633368"
variation 2109
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1358635527"
variation 2110..2126
/gene="SEMA4G"
/replace="ga"
/replace="gatacaggacatagaga"
/db_xref="dbSNP:1435619713"
variation 2112
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1271640141"
variation 2115
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:764114736"
variation 2116
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:995770723"
variation 2121
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851053214"
variation 2122..2129
/gene="SEMA4G"
/replace="agag"
/replace="agagagag"
/db_xref="dbSNP:767881320"
variation 2123
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1325570015"
variation 2125
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:190201835"
variation 2126
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851053643"
variation 2128
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851053737"
variation 2134
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:538842540"
variation 2135
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851053925"
variation 2136
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:757411949"
variation 2140
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133889080"
variation 2144
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:781378063"
variation 2145
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:746282456"
variation 2147
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1231622802"
variation 2148
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1279237287"
variation 2150
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:756467836"
variation 2152
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:369529769"
variation 2155
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851054882"
variation 2157
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:534283434"
exon 2163..4474
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 2163
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1373085610"
variation 2164
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851211935"
variation 2165..2177
/gene="SEMA4G"
/replace="ccaccaccac"
/replace="ccaccaccaccac"
/replace="ccaccaccaccaccac"
/db_xref="dbSNP:145835827"
variation 2165..2166
/gene="SEMA4G"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1554884798"
variation 2167
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1334008977"
variation 2171
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1327563265"
variation 2173
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851212995"
variation 2177..2179
/gene="SEMA4G"
/replace=""
/replace="ctg"
/db_xref="dbSNP:755081302"
variation 2181
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:552270687"
variation 2184
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1341977736"
variation 2185
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1235282106"
variation 2186
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1282755788"
variation 2187
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:754085049"
variation 2192
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1589998314"
variation 2195
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1199969523"
variation 2198
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:760031264"
variation 2199
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:753257306"
variation 2201
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133901396"
variation 2202
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:773478369"
variation 2203
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:778125924"
variation 2208
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:570573396"
variation 2210
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1175068535"
variation 2215
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:755545892"
variation 2218
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:779730408"
variation 2220
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1158667773"
variation 2223
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:748889973"
variation 2224
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1384413039"
variation 2227
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:768472015"
variation 2228
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:761068926"
variation 2231
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1442105033"
variation 2232
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851217451"
variation 2233
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851217575"
variation 2235
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1305846909"
variation 2236
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:183718929"
variation 2237
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1232869244"
variation 2239
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:549851109"
variation 2242
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1245506254"
variation 2243
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1353024006"
variation 2246
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:146245319"
variation 2247
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:760851566"
variation 2248
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851218914"
variation 2249
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851219065"
variation 2251
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:770897727"
variation 2253
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1195301504"
variation 2254
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1264768450"
variation 2257
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:777019767"
variation 2259
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:759761969"
variation 2260
/gene="SEMA4G"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1005161073"
variation 2261
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:201001972"
variation 2265
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1451010139"
variation 2266
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851220823"
variation 2271
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1157499811"
variation 2273
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:776051888"
variation 2274
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851221493"
variation 2275
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1005716850"
variation 2276
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851222036"
variation 2280
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851222273"
variation 2281
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1017136365"
variation 2283
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:763219828"
variation 2284
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:764701072"
variation 2285
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:137971825"
variation 2287
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:755671543"
variation 2289
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851223790"
variation 2290
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851224022"
variation 2291
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1355476316"
variation 2292
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1589998686"
variation 2293..2295
/gene="SEMA4G"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1251708384"
variation 2293
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:977978033"
variation 2294
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:765835066"
variation 2295
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851225605"
variation 2296
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1589998724"
variation 2299
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:753494547"
variation 2300
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1315808916"
variation 2302
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1287605179"
variation 2303
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:149389232"
variation 2304
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:144727154"
variation 2305
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851227514"
variation 2308
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:748043373"
variation 2310
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851228007"
variation 2311
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:148516703"
variation 2312
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:374200198"
variation 2314
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851228915"
variation 2317
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:142773171"
variation 2318
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:147237913"
variation 2326
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851229807"
variation 2327
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:141030743"
variation 2329
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851230304"
variation 2332
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851230541"
variation 2335..2336
/gene="SEMA4G"
/replace=""
/replace="tg"
/db_xref="dbSNP:1851230987"
variation 2335
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851230778"
variation 2336
/gene="SEMA4G"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1851231197"
variation 2338
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:770205655"
variation 2341
/gene="SEMA4G"
/replace=""
/replace="g"
/db_xref="dbSNP:1851231852"
variation 2341
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851231625"
variation 2342..2343
/gene="SEMA4G"
/replace=""
/replace="aa"
/db_xref="dbSNP:1851232419"
variation 2342
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:775542275"
variation 2343
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851232649"
variation 2344
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851232858"
variation 2345
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851233038"
variation 2345
/gene="SEMA4G"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1851233269"
variation 2347
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851233489"
variation 2356
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:755113434"
variation 2357
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:764316566"
variation 2362
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:774952582"
variation 2365
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133902664"
variation 2368
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:762161081"
variation 2370
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1298897763"
variation 2373
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851235035"
variation 2374
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:765887043"
variation 2375
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:753406520"
variation 2376
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1408024389"
variation 2380
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851235974"
variation 2383
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:754482102"
variation 2384
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1307475986"
variation 2386
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:764912089"
variation 2387
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:539263557"
variation 2388
/gene="SEMA4G"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1851237219"
variation 2390
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:866091256"
variation 2391
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:558586100"
variation 2392
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:777395006"
variation 2393
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1589998968"
variation 2394
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851238350"
variation 2395
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851238569"
variation 2396
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1049622681"
variation 2397
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:746976668"
variation 2398
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:940882437"
variation 2404
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:757318232"
variation 2407
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851239938"
variation 2409
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851240164"
variation 2410
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1444392472"
variation 2412
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1204049997"
variation 2413
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851240875"
variation 2416
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:977211113"
variation 2418
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851241278"
variation 2419
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1257594428"
variation 2422
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1486401615"
variation 2423
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:781268916"
variation 2424
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:144879682"
variation 2425
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1423563944"
variation 2426
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851242706"
variation 2429
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1171588564"
variation 2431..2433
/gene="SEMA4G"
/replace="cac"
/replace="cacac"
/db_xref="dbSNP:1392472908"
variation 2434
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851243412"
variation 2438
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:902133075"
variation 2440
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851243897"
variation 2442
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851244159"
variation 2444
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851244380"
variation 2450
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851244630"
variation 2453
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1168271228"
variation 2454
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1376084022"
variation 2456
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1416703361"
variation 2459
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:775801456"
variation 2465
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1378378322"
variation 2466
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:997799025"
variation 2467
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851245990"
variation 2470
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:749431067"
variation 2471
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1339881664"
variation 2475
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1031887205"
variation 2477
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:769068051"
variation 2479
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1589999247"
variation 2480
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:774521972"
variation 2481
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1207455851"
variation 2482
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:762152467"
variation 2483
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:772635727"
variation 2484
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851247954"
variation 2485..2489
/gene="SEMA4G"
/replace="tg"
/replace="tgatg"
/db_xref="dbSNP:1187659489"
variation 2485
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851248197"
variation 2486
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851248500"
variation 2488
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851248659"
variation 2489
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:957195278"
variation 2494
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1589999321"
variation 2495
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851249179"
variation 2496
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:759100020"
variation 2497
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1448113201"
variation 2498
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851249681"
variation 2499
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:990022918"
variation 2501
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1395953506"
variation 2502
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:544195173"
variation 2503
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851250291"
variation 2505
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:752430522"
variation 2507
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1358691563"
variation 2512
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1224493460"
variation 2516
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1454241106"
variation 2517
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1265325492"
variation 2518..2522
/gene="SEMA4G"
/replace="c"
/replace="cgcgc"
/db_xref="dbSNP:1851251239"
variation 2518
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:147942823"
variation 2519
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:140546736"
variation 2520
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:751374543"
variation 2521..2522
/gene="SEMA4G"
/replace=""
/replace="tata"
/db_xref="dbSNP:1851251846"
variation 2521
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:757083877"
variation 2524
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1589999484"
variation 2525
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:149914326"
variation 2526
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:750335846"
variation 2535..2550
/gene="SEMA4G"
/replace="gcctcatcctggcctc"
/replace="gcctcatcctggcctcatcctggcctc"
/db_xref="dbSNP:1851252713"
variation 2535
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1380369416"
variation 2537
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:756293264"
variation 2539
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:779930213"
variation 2543
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851253195"
variation 2547
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:939406010"
variation 2548
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:749539011"
variation 2549
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1270578063"
variation 2550
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:71488078"
variation 2551
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851254045"
variation 2553
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:768819125"
variation 2555
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:144937502"
variation 2559..2561
/gene="SEMA4G"
/replace=""
/replace="tct"
/db_xref="dbSNP:569204913"
variation 2562
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:748554644"
variation 2563
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851254882"
variation 2564
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1210510722"
variation 2567
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:887229636"
variation 2568
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:772406976"
variation 2569
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851255424"
variation 2575
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851255543"
variation 2576
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:773734595"
variation 2577
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:761134134"
variation 2580
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851256014"
variation 2582
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:769355889"
variation 2583
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:774916385"
variation 2588
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:542184127"
variation 2589
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1326312908"
variation 2590
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851256871"
variation 2592
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:763691852"
variation 2593
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851257157"
variation 2594
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:149052530"
variation 2595
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:41291464"
variation 2596
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851257680"
variation 2597
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1242957860"
variation 2598
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:527848892"
variation 2599
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851258036"
variation 2600
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:756057332"
variation 2601
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:780027867"
variation 2602
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851258594"
variation 2604
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413539150"
variation 2606
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:200288019"
variation 2607..2613
/gene="SEMA4G"
/replace="act"
/replace="actcact"
/db_xref="dbSNP:748396129"
variation 2607
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1327673019"
variation 2610
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1208690414"
variation 2611
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851259631"
variation 2612
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1274190195"
variation 2614
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133904692"
variation 2615
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1159862173"
variation 2618
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:138505815"
variation 2619
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:140405167"
variation 2623
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851260166"
variation 2624
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1473694674"
variation 2627
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:779055594"
variation 2628
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:531476226"
variation 2630
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1286873399"
variation 2632
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:778047878"
variation 2634
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:145555722"
variation 2635..2660
/gene="SEMA4G"
/replace="ag"
/replace="aggatctgcggtgcaactgcagacag"
/db_xref="dbSNP:1351574365"
variation 2635
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1472206434"
variation 2636
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:771404491"
variation 2637
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415680566"
variation 2638
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851262875"
variation 2639
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851263063"
variation 2641
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851263236"
variation 2643
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:777161655"
variation 2644
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:138067900"
variation 2645
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1282725183"
variation 2647
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1354773723"
variation 2648
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1411329720"
variation 2650
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851264505"
variation 2652
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1305609497"
variation 2653
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851264866"
variation 2657..2659
/gene="SEMA4G"
/replace="a"
/replace="aca"
/db_xref="dbSNP:1349407594"
variation 2658
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1228303776"
variation 2659
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851265432"
variation 2660
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1285314078"
variation 2666
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1358827837"
variation 2673
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1226997498"
variation 2676
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:375760083"
variation 2679
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1438587910"
variation 2681
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:774176474"
variation 2683
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1249714433"
variation 2684
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:761489347"
variation 2685
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1188499233"
variation 2687..2706
/gene="SEMA4G"
/replace="gatgagggtgatgatgaggg"
/replace="gatgagggtgatgatgagggtgatgatgaggg"
/db_xref="dbSNP:772358119"
variation 2689
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:767433560"
variation 2690..2693
/gene="SEMA4G"
/replace="g"
/replace="gagg"
/db_xref="dbSNP:1851267553"
variation 2692
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:773199318"
variation 2693
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:760515196"
variation 2694
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1359315768"
variation 2700
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:145330425"
variation 2702
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:753794838"
variation 2702
/gene="SEMA4G"
/replace="g"
/replace="gg"
/replace="gggg"
/db_xref="dbSNP:1851268481"
variation 2703
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133905431"
variation 2704..2715
/gene="SEMA4G"
/replace="gggggctggggg"
/replace="gggggctggggggctggggg"
/db_xref="dbSNP:1406962803"
variation 2704..2708
/gene="SEMA4G"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1411362753"
variation 2704..2705
/gene="SEMA4G"
/replace=""
/replace="aa"
/db_xref="dbSNP:1851269415"
variation 2704
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:755038247"
variation 2706
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1369335681"
variation 2707
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1414869947"
variation 2708
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851270194"
variation 2709..2720
/gene="SEMA4G"
/replace="ctgggggcctgg"
/replace="ctgggggcctgggggcctgg"
/db_xref="dbSNP:1475018399"
variation 2709
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1335400856"
variation 2710
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590000321"
variation 2712
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1342807731"
variation 2715
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:565974154"
variation 2716
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590000368"
variation 2718
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1283942354"
variation 2722
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:927913032"
variation 2723
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851271928"
variation 2724
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1230873584"
variation 2725
/gene="SEMA4G"
/replace=""
/replace="c"
/db_xref="dbSNP:1487389551"
variation 2725
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851272264"
variation 2726
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851272553"
variation 2727
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1272774402"
variation 2729
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:752924036"
variation 2730
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1201126917"
variation 2731
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851273137"
variation 2734
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:539199769"
variation 2736
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:889434035"
variation 2738
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851273660"
variation 2743
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1011010207"
variation 2746
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851273972"
variation 2752
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851274114"
variation 2755
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:200801941"
variation 2756..2757
/gene="SEMA4G"
/replace=""
/replace="gc"
/replace="gccc"
/replace="gcccc"
/replace="gccccc"
/replace="gcccccc"
/replace="gccccccc"
/db_xref="dbSNP:rs1851274585"
variation 2756
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851274273"
variation 2756
/gene="SEMA4G"
/replace="g"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1554885050"
variation 2757..2761
/gene="SEMA4G"
/replace=""
/replace="cccca"
/db_xref="dbSNP:1851275324"
variation 2757..2760
/gene="SEMA4G"
/replace="ccc"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1307646381"
variation 2757
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1564800318"
variation 2758..2765
/gene="SEMA4G"
/replace="ccc"
/replace="cccagccc"
/db_xref="dbSNP:1451113011"
variation 2758
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1490149544"
variation 2759
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1319007353"
variation 2761..2762
/gene="SEMA4G"
/replace=""
/replace="ag"
/db_xref="dbSNP:1244403035"
variation 2761
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:747411482"
variation 2762
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:757616280"
variation 2762
/gene="SEMA4G"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1851276615"
variation 2763..2778
/gene="SEMA4G"
/replace="ccccacc"
/replace="ccccaccacccccacc"
/db_xref="dbSNP:1851277127"
variation 2763..2766
/gene="SEMA4G"
/replace="cccc"
/replace="ccccccccccc"
/replace="ccccccccccccccc"
/db_xref="dbSNP:1564800345"
variation 2763
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1389197846"
variation 2764
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1434747606"
variation 2766..2771
/gene="SEMA4G"
/replace="c"
/replace="caccac"
/db_xref="dbSNP:1173800017"
variation 2766
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133906339"
variation 2767..2770
/gene="SEMA4G"
/replace=""
/replace="acca"
/db_xref="dbSNP:1399486489"
variation 2767
/gene="SEMA4G"
/replace=""
/replace="a"
/db_xref="dbSNP:1851277715"
variation 2767
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1326270062"
variation 2768
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:781570245"
variation 2769
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:746344453"
variation 2770
/gene="SEMA4G"
/replace=""
/replace="a"
/db_xref="dbSNP:1851278531"
variation 2770
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1438563345"
variation 2771..2790
/gene="SEMA4G"
/replace="cccccaccgcc"
/replace="cccccaccgcccccaccgcc"
/replace="cccccaccgcccccaccgcccccaccgcc"
/db_xref="dbSNP:773176617"
variation 2771..2775
/gene="SEMA4G"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:746736051"
variation 2772
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1334155427"
variation 2773
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:570600855"
variation 2776
/gene="SEMA4G"
/replace=""
/replace="a"
/db_xref="dbSNP:1366311394"
variation 2776
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1437736186"
variation 2777
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1465984153"
variation 2778
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:537981098"
variation 2779
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1364699879"
variation 2781
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1234288227"
variation 2783
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590000861"
variation 2785
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1257825267"
variation 2786
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1476929728"
variation 2787
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:773939741"
variation 2788
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1199749295"
variation 2791
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1268693928"
variation 2792
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:771918484"
variation 2793
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:772968534"
variation 2794
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:368791581"
variation 2795
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1454424276"
variation 2797
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133906812"
variation 2798
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1200638891"
variation 2800
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:766151814"
variation 2804
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:983229924"
variation 2805
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:776467523"
variation 2808
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:908616884"
variation 2809
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:759454826"
variation 2812
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:765317734"
variation 2813
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851283080"
variation 2814
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:941479176"
variation 2815
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:752836080"
variation 2816
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1318914837"
variation 2817
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1590001080"
variation 2824
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:764345648"
variation 2825
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851284021"
variation 2827
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1387547863"
variation 2830
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1303695342"
variation 2831
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:556496771"
variation 2832
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:757591403"
variation 2837
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:574711696"
variation 2838
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1331107517"
variation 2839
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851285121"
variation 2840
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1590001162"
variation 2841
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:781551217"
variation 2842
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1220506232"
variation 2843
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1590001187"
variation 2844
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1407498903"
variation 2848
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:746374262"
variation 2854
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851286122"
variation 2856
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:756701345"
variation 2857
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1211209380"
variation 2859
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851286938"
variation 2865
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:780702310"
variation 2866
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851287302"
variation 2871
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:747701115"
variation 2872
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:771687718"
variation 2875
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1413580384"
variation 2876
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:962140588"
variation 2877
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:976145243"
variation 2883
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:777592361"
variation 2884
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1157657574"
variation 2888
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1402208941"
variation 2890
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851288279"
variation 2891
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1411611036"
variation 2892
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1460684927"
variation 2894
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851288704"
variation 2895
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851288842"
variation 2898
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:921452117"
variation 2899
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851289124"
variation 2900
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1590001329"
variation 2905
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:376187099"
variation 2907
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1295465666"
variation 2911
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:776432076"
variation 2912
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1386472605"
variation 2914
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:141726768"
variation 2915
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:769758760"
variation 2918
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:554126222"
variation 2920
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851290572"
variation 2923
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851290768"
variation 2927
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:199549347"
variation 2928
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:764116745"
variation 2932
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:986379770"
variation 2936
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1246763144"
variation 2938
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1227060568"
variation 2941
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851291821"
variation 2942
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1177109703"
variation 2943
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1263267741"
variation 2949
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851292306"
variation 2950
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:751732798"
variation 2951
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1287154805"
variation 2952
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:150436471"
variation 2953
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:750866450"
variation 2954
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851292761"
variation 2959
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:756516259"
variation 2960
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:375024485"
variation 2962
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851293256"
variation 2963
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1250475715"
variation 2965
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1424709004"
variation 2966
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:754349112"
variation 2968
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851293867"
variation 2969
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1367130443"
variation 2970
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1424259786"
variation 2971
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:369095063"
variation 2972
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1372422706"
variation 2973
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1222819487"
variation 2975
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1590001608"
variation 2977
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:138231164"
variation 2979
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1052793166"
variation 2980
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1307300351"
variation 2981..2988
/gene="SEMA4G"
/replace="tctg"
/replace="tctgtctg"
/db_xref="dbSNP:1851296377"
variation 2983
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:149579572"
variation 2983
/gene="SEMA4G"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1056241246"
variation 2988
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851297087"
variation 2990
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1012519597"
variation 2991
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851297556"
variation 2993
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851297775"
variation 2994
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:770679319"
variation 2998
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851298209"
variation 2999..3000
/gene="SEMA4G"
/replace=""
/replace="g"
/db_xref="dbSNP:1851298451"
variation 3005
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:780708778"
variation 3006
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1011343221"
variation 3010
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:745721149"
variation 3011
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1276335802"
variation 3014
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:769527048"
variation 3015
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851299997"
variation 3019
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:879129411"
variation 3021
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1373716210"
variation 3022
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:775434918"
variation 3023
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:762807711"
variation 3029
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1483848011"
variation 3032
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:768734270"
variation 3039
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851301714"
variation 3042
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1173041083"
variation 3045
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:969880106"
variation 3046
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1003167771"
variation 3055
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1180250824"
variation 3057
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1257290025"
variation 3066
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851302969"
variation 3069..3071
/gene="SEMA4G"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1183256014"
variation 3071
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1482030451"
variation 3073..3075
/gene="SEMA4G"
/replace="ccc"
/replace="ccccc"
/db_xref="dbSNP:1256227888"
variation 3073
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133908720"
variation 3074
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1023540260"
variation 3081
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851304104"
variation 3084
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1436403588"
variation 3085
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:887726997"
variation 3087
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133908809"
variation 3088
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851304584"
variation 3089
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:781204292"
variation 3092
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851305040"
variation 3094
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1014839064"
variation 3097
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851305511"
variation 3098
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:962032640"
variation 3112
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:976114197"
variation 3114
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:745690393"
variation 3117
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851306652"
variation 3118
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851306867"
variation 3119
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851307077"
variation 3128
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851307315"
variation 3133
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:950718210"
variation 3135..3136
/gene="SEMA4G"
/replace=""
/replace="ag"
/db_xref="dbSNP:1590001957"
variation 3138..3163
/gene="SEMA4G"
/replace=""
/replace="caggcccagccaaagccccctcctca"
/db_xref="dbSNP:1590001967"
variation 3140
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851308106"
variation 3141
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851308337"
variation 3142
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:953557741"
variation 3143
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1362537886"
variation 3147
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:986736713"
variation 3151
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:982791219"
variation 3153..3157
/gene="SEMA4G"
/replace="ccccc"
/replace="cccccc"
/db_xref="dbSNP:1851309403"
variation 3154
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1410299026"
variation 3159
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:908564430"
variation 3162..3163
/gene="SEMA4G"
/replace=""
/replace="ca"
/db_xref="dbSNP:2133909252"
variation 3165
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:962745699"
variation 3166
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1453609825"
variation 3168
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:974131731"
variation 3169
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:921398275"
variation 3170
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851310611"
variation 3171
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1308719600"
variation 3175
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133909360"
variation 3178
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1564800882"
variation 3182
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851311037"
variation 3184
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1416775905"
variation 3186
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851311226"
variation 3187
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1193893340"
variation 3189
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:932827701"
variation 3192
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1385143611"
variation 3194
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:947584470"
variation 3196
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:977712151"
variation 3198
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1242406016"
variation 3199
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851312352"
variation 3200
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1333845024"
variation 3201
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:564705467"
variation 3202
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:912794871"
variation 3203
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1342470994"
variation 3205
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1331866472"
variation 3210
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851313372"
variation 3220
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851313579"
variation 3224
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1316233169"
variation 3225..3227
/gene="SEMA4G"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1382183614"
variation 3230
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851314310"
variation 3231
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:531413037"
variation 3237
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1460240665"
variation 3239..3246
/gene="SEMA4G"
/replace="tgc"
/replace="tgccctgc"
/db_xref="dbSNP:1236997858"
variation 3240
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1171020858"
variation 3241
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851315304"
variation 3243
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1478564784"
variation 3245
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:757063742"
variation 3247
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1191784859"
variation 3249
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1433241980"
variation 3251
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851316321"
variation 3254
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1269427005"
variation 3270..3279
/gene="SEMA4G"
/replace="cctaa"
/replace="cctaacctaa"
/db_xref="dbSNP:1342086795"
variation 3273
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:543028700"
variation 3276
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851317105"
variation 3282
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2295717"
variation 3287
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:781060343"
variation 3291
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851317720"
variation 3292
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:561836841"
variation 3293
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851318174"
variation 3296
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:745805497"
variation 3297
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:947905136"
variation 3299..3300
/gene="SEMA4G"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1242415993"
variation 3299
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851318713"
variation 3300
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:774547564"
variation 3302
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1304136053"
variation 3304..3312
/gene="SEMA4G"
/replace="c"
/replace="ctcctgttc"
/db_xref="dbSNP:1439323352"
variation 3304
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1394221728"
variation 3308
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1332383377"
variation 3311
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851319701"
variation 3312
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:887621111"
variation 3313
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1006521433"
variation 3315
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2295716"
variation 3316
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1035962765"
variation 3322..3323
/gene="SEMA4G"
/replace="gc"
/replace="gcgc"
/db_xref="dbSNP:374469923"
variation 3324
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:767847442"
variation 3329
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1165781151"
variation 3330
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:547371500"
variation 3331..3336
/gene="SEMA4G"
/replace="ct"
/replace="ctttct"
/db_xref="dbSNP:1564801033"
variation 3332..3334
/gene="SEMA4G"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1851321381"
variation 3338
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590002545"
variation 3342
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851321658"
variation 3346
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851321816"
variation 3347
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1427851024"
variation 3348
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1169802472"
variation 3351
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133910482"
variation 3353
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1358850075"
variation 3357
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:761133475"
variation 3358
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1191685942"
variation 3359
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851322719"
variation 3361
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:565832622"
variation 3362
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1301023166"
variation 3364
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1238599331"
variation 3365
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:140873008"
variation 3366..3369
/gene="SEMA4G"
/replace="atat"
/replace="atatat"
/db_xref="dbSNP:1180219371"
variation 3367
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:775161961"
variation 3368
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851323614"
variation 3370
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1435583593"
variation 3371
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1347264509"
variation 3377
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:755490675"
variation 3378
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1022174562"
variation 3379
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851324366"
variation 3381
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1282490941"
variation 3390
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1232746478"
variation 3392
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851325083"
variation 3398..3400
/gene="SEMA4G"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1564801111"
variation 3398
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1015510000"
variation 3401
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:551143626"
variation 3403
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1309192746"
variation 3404
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1446522565"
variation 3405
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851326399"
variation 3407
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1313501848"
variation 3409
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851326936"
variation 3410
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851327156"
variation 3412
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1381487456"
variation 3418
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1370845164"
variation 3427
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1212785459"
variation 3428
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:962694375"
variation 3429
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851328377"
variation 3432
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:11591349"
variation 3433
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:536866327"
variation 3434
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1250348904"
variation 3438
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1447859281"
variation 3439
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1186203566"
variation 3440
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:977649336"
variation 3443
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133911153"
variation 3447
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:756712868"
variation 3450
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1204147027"
variation 3451
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:556345883"
variation 3452
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1434047317"
variation 3454
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851330601"
variation 3456
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1173815254"
variation 3457
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:567995095"
variation 3458
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:986972740"
variation 3461
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1322261528"
variation 3467
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1386272160"
variation 3468
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1468467340"
variation 3469
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851331669"
variation 3470
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:745459702"
variation 3472
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:755937099"
variation 3473
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851332127"
variation 3476
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242453332"
variation 3477
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:11190780"
variation 3478
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1369013608"
variation 3482
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1217004954"
variation 3484
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:749061715"
variation 3492
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1323427412"
variation 3493
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:768679541"
variation 3494
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:562213978"
variation 3497
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1463832678"
variation 3498
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1215245125"
variation 3500
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1392099800"
variation 3503
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1247539943"
variation 3504
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851334603"
variation 3506
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1489476783"
variation 3507
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851335052"
variation 3512
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:774150942"
variation 3513
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1330576370"
variation 3514
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:554180516"
variation 3515
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1161357971"
variation 3516
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1222920929"
variation 3521..3525
/gene="SEMA4G"
/replace="ct"
/replace="cttct"
/db_xref="dbSNP:1409419478"
variation 3524..3528
/gene="SEMA4G"
/replace="ct"
/replace="ctcct"
/db_xref="dbSNP:1399901647"
variation 3529
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851337089"
variation 3530
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1164988814"
variation 3532
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1347204536"
variation 3535..3539
/gene="SEMA4G"
/replace="tt"
/replace="ttctt"
/db_xref="dbSNP:1851337943"
variation 3537
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1351283007"
variation 3539
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851338509"
variation 3545
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:748317224"
variation 3548
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1301958846"
variation 3552
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851339309"
variation 3557
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1350650732"
variation 3558
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:771987099"
variation 3559
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:909015462"
variation 3560
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:947024954"
variation 3562
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1348931588"
variation 3578
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1044109678"
variation 3579
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851341027"
variation 3587
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851341287"
variation 3591
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851341554"
variation 3593
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1223598937"
variation 3596
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:941896553"
variation 3602
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1590003340"
variation 3603..3606
/gene="SEMA4G"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:749161619"
variation 3603
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:867056759"
variation 3605
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851342959"
variation 3606
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1341846221"
variation 3610
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1323698735"
variation 3613
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1219725456"
variation 3614
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:897779980"
variation 3615
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1483432059"
variation 3617
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:766759551"
variation 3618
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133912160"
variation 3620
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1398820091"
variation 3623
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:938445182"
variation 3624
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1249568875"
variation 3626..3628
/gene="SEMA4G"
/replace="t"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:1564801421"
variation 3634
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851345504"
variation 3636
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851345730"
variation 3638
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133912278"
variation 3640..3642
/gene="SEMA4G"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:34661749"
variation 3640
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1469396700"
variation 3642
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1590003500"
variation 3645
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1051674712"
variation 3646
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1473643656"
variation 3647
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415748001"
variation 3653
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1403242646"
variation 3655
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851347694"
variation 3656
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851347910"
variation 3657
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413115744"
variation 3661
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1186071819"
variation 3662
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1162547813"
variation 3663
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1370560535"
variation 3669
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:889128459"
variation 3670
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851348837"
variation 3671
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1431132181"
variation 3676..3684
/gene="SEMA4G"
/replace="ctcc"
/replace="ctcccctcc"
/db_xref="dbSNP:1310336433"
variation 3678
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851349496"
variation 3679
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1056944101"
variation 3682
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851350086"
variation 3684
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:886274992"
variation 3686
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1828080527"
variation 3689..3695
/gene="SEMA4G"
/replace="cct"
/replace="ccttcct"
/db_xref="dbSNP:1442168150"
variation 3689
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1285150909"
variation 3690
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:150176473"
variation 3693
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1284040676"
variation 3698
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1243979563"
variation 3700
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1454985511"
variation 3704
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1016127185"
variation 3705
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1342914307"
variation 3706
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1207413139"
variation 3709
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1272637340"
variation 3711..3716
/gene="SEMA4G"
/replace=""
/replace="atcagc"
/db_xref="dbSNP:1437134295"
variation 3711
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:546548368"
variation 3714..3723
/gene="SEMA4G"
/replace=""
/replace="agcctcccca"
/db_xref="dbSNP:1232285107"
variation 3717
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851353656"
variation 3718
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851353903"
variation 3719..3722
/gene="SEMA4G"
/replace="ccc"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1851354331"
variation 3719
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:999055334"
variation 3720..3724
/gene="SEMA4G"
/replace="c"
/replace="cccac"
/db_xref="dbSNP:1188248769"
variation 3721
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:558511473"
variation 3723
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851355064"
variation 3724
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1471688492"
variation 3725..3726
/gene="SEMA4G"
/replace=""
/replace="gtgtga"
/db_xref="dbSNP:1279740182"
variation 3725
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564801584"
variation 3726
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1182551535"
variation 3732
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1390425592"
variation 3733
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:866465441"
variation 3735
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:899127927"
variation 3736
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851356441"
variation 3742..3743
/gene="SEMA4G"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1851356699"
variation 3747..3749
/gene="SEMA4G"
/replace="t"
/replace="tat"
/db_xref="dbSNP:776469814"
variation 3747
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:1564801613"
variation 3748
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:995448141"
variation 3749
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1406943937"
variation 3750..3755
/gene="SEMA4G"
/replace="gaga"
/replace="gagaga"
/db_xref="dbSNP:1031921038"
variation 3751
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1352660512"
variation 3752
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1166136937"
variation 3754
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:960318556"
variation 3758
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851358185"
variation 3763
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1217254719"
variation 3766
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:993082702"
variation 3767
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851358464"
variation 3768
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851358683"
variation 3770
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:576676078"
variation 3771
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851359112"
variation 3773
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:954125817"
variation 3774
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1409881469"
variation 3779
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1590004029"
variation 3780
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1335465291"
variation 3781
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1361197103"
variation 3783
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1450956457"
variation 3789
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1314573273"
variation 3790
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242083934"
variation 3792..3793
/gene="SEMA4G"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1366179476"
variation 3792
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851361189"
variation 3794
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1734059355"
variation 3795..3798
/gene="SEMA4G"
/replace="aaca"
/replace="aacaaca"
/db_xref="dbSNP:398114688"
variation 3796..3803
/gene="SEMA4G"
/replace="acac"
/replace="acacacac"
/db_xref="dbSNP:146737296"
variation 3796
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851362081"
variation 3798
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1470152414"
variation 3799
/gene="SEMA4G"
/replace=""
/replace="c"
/db_xref="dbSNP:1554885387"
variation 3801..3804
/gene="SEMA4G"
/replace="c"
/replace="cacc"
/db_xref="dbSNP:1564801730"
variation 3801
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:980911684"
variation 3809
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:908989869"
variation 3810
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1318120156"
variation 3813
/gene="SEMA4G"
/replace=""
/replace="a"
/db_xref="dbSNP:1851363694"
variation 3814
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1297128475"
variation 3815..3816
/gene="SEMA4G"
/replace=""
/replace="at"
/db_xref="dbSNP:201653131"
variation 3816
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851363979"
variation 3817
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:941859324"
variation 3819
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1275426272"
variation 3825
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:544003449"
variation 3832
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:561580399"
variation 3837
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:987306998"
variation 3838
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1761267634"
variation 3844
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851365080"
variation 3845
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:760046546"
variation 3848
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851365638"
variation 3856
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:570837619"
variation 3858
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851366097"
variation 3859
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1461145737"
variation 3860
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:956410819"
variation 3864
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1172757131"
variation 3865
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590004294"
variation 3869
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:765696472"
variation 3870..3877
/gene="SEMA4G"
/replace="ctgt"
/replace="ctgtctgt"
/db_xref="dbSNP:1851367609"
variation 3870
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851367435"
variation 3872
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:776736066"
variation 3884
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:541757083"
variation 3885
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1455911411"
variation 3887
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133914046"
variation 3889
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:947649741"
variation 3890
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:540658889"
variation 3895
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1458477096"
variation 3897
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851368804"
variation 3912
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:979738620"
variation 3913
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133914138"
variation 3914
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1419920691"
variation 3932
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851369510"
variation 3935
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:926970920"
variation 3937
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:938406307"
variation 3944
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1345587818"
variation 3949..3957
/gene="SEMA4G"
/replace="ggatg"
/replace="ggatggatg"
/db_xref="dbSNP:1156991738"
variation 3950
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1590004435"
variation 3955
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1411538590"
variation 3956
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1447292211"
variation 3957
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1057292576"
variation 3967
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1401448436"
variation 3968
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:148889377"
variation 3970
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1354019972"
variation 3973
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1357855929"
variation 3974
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:185501392"
variation 3975
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1437149072"
variation 3976
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1393859490"
variation 3979
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1314077837"
variation 3983..3984
/gene="SEMA4G"
/replace="c"
/replace="cc"
/db_xref="dbSNP:745620184"
variation 3989
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851373532"
variation 3990
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1357883329"
variation 3992
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1058101"
variation 3993..3997
/gene="SEMA4G"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1564801889"
variation 3994
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1043523463"
variation 3996
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1440759734"
variation 3997
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1037520890"
variation 3998
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851374834"
variation 4004
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851375125"
variation 4008
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851375359"
variation 4013..4017
/gene="SEMA4G"
/replace="tc"
/replace="tcctc"
/db_xref="dbSNP:1851375586"
variation 4014
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1287105200"
variation 4015
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:899075093"
variation 4017
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851376270"
variation 4018
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:758453345"
variation 4019
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:999022475"
variation 4021
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:533032857"
variation 4023
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851377123"
variation 4028
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851377286"
variation 4030..4038
/gene="SEMA4G"
/replace="gggaaaggg"
/replace="gggaaagggggaaaggg"
/db_xref="dbSNP:1237569905"
variation 4030
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1276666015"
variation 4036
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851377980"
variation 4037..4043
/gene="SEMA4G"
/replace="ggag"
/replace="ggaggag"
/db_xref="dbSNP:1212458091"
variation 4043
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:539958411"
variation 4049
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1031806643"
variation 4051
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:996061169"
variation 4052..4056
/gene="SEMA4G"
/replace="tgtct"
/replace="tgtctgtct"
/db_xref="dbSNP:1851379088"
variation 4052..4054
/gene="SEMA4G"
/replace="t"
/replace="tgt"
/db_xref="dbSNP:1851378916"
variation 4053
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1276056518"
variation 4054
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1318520975"
variation 4057
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851379758"
variation 4060
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1028300853"
variation 4061
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1222315298"
variation 4066
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:145456828"
variation 4068
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851380461"
variation 4072
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1259577119"
variation 4073
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851380817"
variation 4074
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851380992"
variation 4080
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:969446661"
variation 4084
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851381422"
variation 4088
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1313689869"
variation 4089
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851381840"
variation 4092
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851382067"
variation 4098
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:980495734"
variation 4100
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1016423976"
variation 4102
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851382772"
variation 4106
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:764283941"
variation 4107
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851383229"
variation 4108
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851383454"
variation 4109
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:889784981"
variation 4110
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851383892"
variation 4115
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851384118"
variation 4116
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1482005638"
variation 4117
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1008277694"
variation 4118
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:751801892"
variation 4124
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133915301"
variation 4129
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1590004825"
variation 4132
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851385217"
variation 4133..4134
/gene="SEMA4G"
/replace=""
/replace="ct"
/db_xref="dbSNP:971792769"
variation 4133
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851385462"
variation 4134
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:919060865"
variation 4136
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851386135"
variation 4145
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851386346"
variation 4146
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1365943648"
variation 4147
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1160574437"
variation 4148
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:549901293"
variation 4149
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851387327"
variation 4150
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:987778470"
variation 4152
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:956145941"
variation 4156
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1189614913"
variation 4157
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1484440106"
variation 4161
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851388353"
variation 4162
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851388576"
variation 4163
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:722435"
variation 4165
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851389219"
variation 4166
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133915599"
variation 4168
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1174615834"
variation 4170
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1377821148"
variation 4171
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1486785377"
variation 4173
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851390176"
variation 4175
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851390425"
variation 4176
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1021817552"
variation 4180
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851390914"
variation 4184
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1258766345"
variation 4185
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:13114"
variation 4187
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:530575708"
variation 4194
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1322070191"
variation 4195
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851392002"
variation 4197
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851392246"
variation 4199
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590005004"
variation 4201
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851392702"
variation 4205
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1294208197"
variation 4208
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851393161"
variation 4213
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:796584525"
variation 4214
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851393640"
variation 4217
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1443718900"
variation 4218
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:549209014"
variation 4219..4223
/gene="SEMA4G"
/replace="ccccc"
/replace="cccccc"
/db_xref="dbSNP:1851394245"
variation 4221
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851394479"
variation 4223
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851394644"
variation 4224
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1272765213"
variation 4225
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:535391514"
variation 4228
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133915982"
variation 4232
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:722434"
variation 4233
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:756150215"
variation 4234
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851395747"
variation 4236..4244
/gene="SEMA4G"
/replace="tga"
/replace="tgaggatga"
/db_xref="dbSNP:1851395903"
variation 4239
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1287595742"
variation 4241
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1590005102"
variation 4242..4247
/gene="SEMA4G"
/replace="tg"
/replace="tgactg"
/db_xref="dbSNP:1282127784"
variation 4246..4248
/gene="SEMA4G"
/replace="t"
/replace="tgt"
/db_xref="dbSNP:1851396880"
variation 4247
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851397104"
variation 4250
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851397297"
variation 4251
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851397538"
variation 4256
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851397765"
variation 4260
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1453577215"
variation 4261
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851398062"
variation 4262
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1339982424"
variation 4267
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:992545494"
variation 4268
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1473984676"
variation 4272
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:377579383"
variation 4275
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1193217573"
variation 4279
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1429752865"
variation 4280
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:535979784"
variation 4282
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851399630"
variation 4283
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1053207362"
variation 4290
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1204475752"
variation 4295
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1468760178"
variation 4298
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851400265"
variation 4299
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:895968520"
variation 4306
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:547453410"
variation 4307
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1215821939"
variation 4310
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1014460178"
variation 4312
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851401422"
variation 4315
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1272754894"
variation 4319
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590005244"
variation 4322
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:566052365"
variation 4323
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1228291159"
variation 4324
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:539856889"
variation 4325..4332
/gene="SEMA4G"
/replace="aatg"
/replace="aatgaatg"
/db_xref="dbSNP:1851402794"
variation 4328
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1294126122"
variation 4331
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:1245235656"
variation 4332
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1023629686"
variation 4341
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:907599520"
variation 4342
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851403820"
variation 4343
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1194666457"
variation 4345
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1459569804"
variation 4348
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851404319"
variation 4351
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1397200065"
variation 4354
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1006217092"
variation 4356
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851405001"
variation 4360
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:940472396"
variation 4364
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1370830712"
variation 4365
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851405676"
variation 4368
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851405873"
variation 4370
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851406098"
variation 4373
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564802346"
variation 4376
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1168572915"
variation 4380
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1454629864"
variation 4384
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851406807"
variation 4390
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1015896546"
variation 4391
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1183846917"
variation 4392
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1590005486"
variation 4393..4394
/gene="SEMA4G"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1851407769"
variation 4393
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1037468969"
variation 4394
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1267016453"
variation 4395
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851408064"
variation 4397
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:971763006"
variation 4398
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:780109310"
variation 4408
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851408894"
variation 4411
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:920446283"
variation 4413
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1590005630"
variation 4414..4419
/gene="SEMA4G"
/replace="ggggag"
/replace="ggggagggggag"
/db_xref="dbSNP:1851409933"
variation 4414
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1026045787"
variation 4415
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1249625499"
variation 4419
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1397803701"
variation 4420
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851410880"
variation 4422
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:11190781"
variation 4423
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851411332"
variation 4425
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:375892284"
variation 4432
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590005760"
variation 4434
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851412105"
variation 4435
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:1348958879"
variation 4435
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590005788"
variation 4438
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1441105677"
variation 4439
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:890411724"
variation 4440
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133917246"
variation 4441
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1008640180"
variation 4442
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:576811967"
variation 4443..4444
/gene="SEMA4G"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1851413621"
variation 4444
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:537243928"
variation 4445
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:555966416"
variation 4446
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:573637014"
variation 4448
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:934667679"
variation 4449
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1171676783"
regulatory 4452..4457
/regulatory_class="polyA_signal_sequence"
/gene="SEMA4G"
/note="hexamer: AATAAA"
variation 4460
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:866768376"
variation 4461
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1010346124"
variation 4462
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851414998"
variation 4463
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851415299"
variation 4467
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:917372450"
variation 4468..4471
/gene="SEMA4G"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1439739794"
variation 4469
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590006249"
variation 4471
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851416502"
polyA_site 4474
/gene="SEMA4G"
/note="major polyA site"
ORIGIN
agccgcggccccttcctctcgcagctggtgctgtggggccgcggagccgcgcgtcgctgtctctatggccccggatccgagcgcaaagaaaacggacctcagaaaaccaggactagctctactgtcgggggcagggtgaccccatcagtaacctacaacccctctagaacttcacaactccctctcaccatggagtttgcatttgatgcagaaaggcatgtgatccctccctccttctgacctcttagctggggattccatggccacacaaccctgtgactccatgtccccccgattccaggaccccccatggccccatgattccttgactcctatgaccttatgacccctgaccttccaagtgacttccttggactttgacccctgtgactgtgcttcccattccccgcccccacaacctgtgactctggctccctttgggggtcttgttagtctgggcctccccaggaagatgtgggggaggctctggcccctcctcctcagcatcctcacagcaactgcagtcccaggaccctcactgcggagaccgtctagagaactagatgccacccctcggatgaccataccctatgaagagctctctgggacccggcacttcaagggccaagcccagaactactcaacactgctgctggaggaggcctcagcaaggctgctggtgggagcccgaggtgccctgttctctctcagtgccaacgacataggagatggggctcacaaagagatccactgggaagcctccccagagatgcaaagcaaatgtcatcaaaaagggaaaaacaaccagacggagtgctttaaccatgtgcggttcctgcagcggctcaattctacccacctctatgcatgtgggactcacgccttccagcccctctgtgcagccattgatgctgaggccttcaccttgccaaccagcttcgaggaggggaaggagaagtgtccttatgacccagcccgtggcttcacaggcctcatcattgatggaggcctctacacagccactaggtatgaattccggagcattcctgacatccgccggagccgccacccacactccctgagaactgaggagacaccaatgcattggctcaatgatgcggagtttgtgttctccgtcctcgtgcgggagagcaaggccagtgcagtgggtgatgatgacaaggtgtactacttcttcacggagcgtgccactgaggagggctctggcagcttcactcagagccgcagcagtcaccgtgtggcccgtgtggctcgtgtctgcaagggagacctgggagggaagaagatcctgcagaagaagtggacttccttcctgaaagcccgtctcatctgccacattccactgtatgagacactgcgtggggtctgcagcctggatgctgaaacctcaagccgtacacacttctatgcagccttcacgctgagcacacagtggaagaccctggaggcctcagccatctgccgctatgacctggcagagatccaggctgtctttgcaggaccctatatggaataccaggatggttcccggcgctggggtcgctatgagggtggggtgcctgagccccggcctggctcgtgtatcacagattcattgcgcagccaaggctacaattcatcccaagacttgccatccctggtcctggactttgtaaagttgcacccactgatggctcggcccgttgtgcccacacgtggacggcccctgctgctcaagcgcaacatacgctacacacaccttacagggacacctgtcaccacgcctgctggacctacctatgacctgctctttctgggcacagctgatggctggatccacaaggccgtagtcctgggctctgggatgcacattattgaagagacacaagtgttcagggagtcccagtctgtggaaaatctagtcatctctctattgcagcacagcctctatgtgggggctcctagcggagtcatccagctaccactctccagctgctcccgctaccgatcctgctatgactgcatcttggcccgagacccctactgtggctgggaccctggcacccatgcctgcgcagcagccaccaccatagccaacaggacagcactgatacaggacatagagagaggaaatcgaggctgtgagagcagcagggatacagggccaccaccaccactgaagacccgctctgtgctccggggtgatgatgtcctcctgccctgtgaccagccatccaacctggcccgggccttgtggctactcaatgggagcatgggcctgagcgatgggcagggtggctaccgtgtgggcgtggacgggctgctggttacagatgcacagcctgagcacagtggcaactatggctgctatgccgaggaaaatggcctccgcaccctgctggcctcctatagtctcacagtccggccagccactcctgccccagctccaaaagcccctgccacacctggggcacagctggcacctgatgtgagactgctctatgtgctagccattgccgcgcttggtggcctctgcctcatcctggcctcctccctcctctatgtggcctgtctgcgggaaggcagacgagggcgccgacggaaatactcactgggtcgggccagccgggcaggaggatctgcggtgcaactgcagacagtctcaggccagtgtcctggagaggaagatgagggtgatgatgagggggctgggggcctggagggcagctgtctccagatcatccctggggagggagccccagccccaccacccccaccgcccccaccgccaccggctgagctgaccaatggcttggtggcactgcccagccggctgcggaggatgaatggcaatagctatgtgcttctgaggcagagcaacaatggagtaccagcagggccctgctccttcgccgaggaactcagccgcatcctggaaaaaaggaagcacacgcagctcgtggagcagctagatgagagctctgtctgagcccagcctcccagaacaaatgctcttccaagccagcctatctgtcccaggctgggccactgcctccctaacacagccaccctcccttcattacccccactccatacccttctcccaactttttgatgtccctgtagggctggccagtcaggcccagccaaagccccctcctcagtctccacagacccacatgtgagcagcccaggcccatcggtgctcctcagaggtaggtgctccctcaggatcaggtgccctgcagacccagagccagttcctatcccctaacctaaacacttataggtgaggactccatcctcctgttccattcatctgcccaaaccctttctctttctcccaggcagggctctgcaggtccatatgggctcaatgtcaccaccctctgcatggccctgtgtgctggatggtcctgaaaccagacaagacctctgccagccacctaagccctgcgtacattcacatgcacacatggaagaatgtttatcggctgggctgcagtgcccccaccctcaccttctcctggtgcattcttgtttcatccctgcttctggacttggggtaccctcccaattgccacatcctatctggtcctcttccccagccccatgtggtgacctctttgtcaagagcttgggaacgggccagcctggggaggtaagactgcatcactcccctcctctcccttcctgtgtggcccttgtgaatcagcctccccactctccttggtcattctcaagagtatgagagacagagctccaggcatgtcccatccccatgcacatgtggtaacacacacctgtatcacacatgtgcttacatttccactcacatgcacctctgagcctcccttgctgtcttggacctgtctgttgggtttagtccgtggacatttcagagggagatccccctcccatttaactgtcctcacaggcccttgcctaggatggatgaccaacactgcactcaatgagccagcctctcttttgggggaatcaagcatttgcttcctctagactacagcagggaaagggaggagaaatctgatgtctcaactggcacatgaagcccattcttggaactatgcaaagggcagaggctgggagtttggacgcttagctcctacccctgtcctacctcaccggggcactttcaggggccaggggcctctgaagtctctaggcctatatgggacaatcaattctgactgagctcccccattcccctcgggtgaggatgactgttatttttgtagctgagaacgtggaatcccacgggtttttactgcccttcacccaacctctcccacctccaccccacaatgaatgtatttattgtgagaatggctacacttctttaggaatgcccccacttacaaccaggtgggtggaacaggcatgtgacagagtggggagcctgggctcagctcctccccctgccgttggttaataaacaccctttttccccaca
//
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]