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Previous release (v1)
2024-04-30 15:50:59, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NR_172054 4575 bp RNA linear PRI 27-JUN-2023
DEFINITION Homo sapiens semaphorin 4G (SEMA4G), transcript variant 6,
non-coding RNA.
ACCESSION NR_172054 XR_945792
VERSION NR_172054.1
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 4575)
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 4575)
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 4575)
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 4575)
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 4575)
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 4575)
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 4575)
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 4575)
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 XR_945792.2.
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##
RNAseq introns :: single sample supports all introns SAMEA1968540,
SAMEA2152474 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: full length.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-88 AL133215.17 52328-52415
89-321 AL133215.17 52516-52748
322-829 AL133215.17 55353-55860
830-978 AL133215.17 55953-56101
979-1041 AL133215.17 56371-56433
1042-1140 AL133215.17 60456-60554
1141-1234 AL133215.17 61119-61212
1235-1348 AL133215.17 61351-61464
1349-1518 AL133215.17 61673-61842
1519-1688 AL133215.17 61926-62095
1689-1833 AL133215.17 62672-62816
1834-2056 AL133215.17 62946-63168
2057-2172 AL133215.17 63402-63517
2173-2333 AL133215.17 63646-63806
2334-2395 AL133215.17 63992-64053
2396-3448 AL133215.17 66129-67181
3449-4575 AL133215.17 67314-68440
FEATURES Location/Qualifiers
source 1..4575
/organism="Homo sapiens"
/mol_type="transcribed RNA"
/db_xref="taxon:9606"
/chromosome="10"
/map="10q24.31"
gene 1..4575
/gene="SEMA4G"
/note="semaphorin 4G"
/db_xref="GeneID:57715"
/db_xref="HGNC:HGNC:10735"
/db_xref="MIM:618991"
misc_RNA 1..4575
/gene="SEMA4G"
/product="semaphorin 4G, transcript variant 6"
/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..321
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 90
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:939127465"
variation 91
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850573955"
variation 93
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850574048"
variation 99
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850574136"
variation 100
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850574227"
variation 102
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850574314"
variation 103
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1589975999"
variation 105
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1589976004"
variation 106..107
/gene="SEMA4G"
/replace=""
/replace="g"
/db_xref="dbSNP:1589976010"
variation 110
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1589976014"
variation 111
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:934300461"
variation 112
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850574831"
variation 113
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1319188151"
variation 117
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:895017755"
variation 119
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850575130"
variation 120
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1166268303"
variation 121
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1393430823"
variation 122
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:995081032"
variation 123
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1041769396"
variation 125
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850575652"
variation 126
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1429836623"
variation 128
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1259031276"
variation 132
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:902878950"
variation 133
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1208076125"
variation 134
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564790593"
variation 135
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850576280"
variation 141
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1468819625"
variation 151
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850576464"
variation 153
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850576569"
variation 154
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850576675"
variation 156
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850576762"
variation 158
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850576857"
variation 163
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1316959859"
variation 167..178
/gene="SEMA4G"
/replace="tgc"
/replace="tgcgcggggtgc"
/db_xref="dbSNP:1048936465"
variation 170
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1589976045"
variation 171
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850577251"
variation 174
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850577316"
variation 175
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1000336668"
variation 178
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1401431037"
variation 182
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1032744188"
variation 183
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1291112691"
variation 184
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:894281176"
variation 186
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1354572986"
variation 189
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1012709363"
variation 192
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1295444003"
variation 193
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1435043732"
variation 196
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1372291222"
variation 200
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850578288"
variation 201
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850578361"
variation 205
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1328353397"
variation 207
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850578535"
variation 208
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1335467398"
variation 214
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850578740"
variation 216
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850578822"
variation 219
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850578908"
variation 220
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1245594158"
variation 222
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850579059"
variation 229
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:543282591"
variation 237
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850579248"
variation 240
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1390454446"
variation 242
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:762356402"
variation 243
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564790627"
variation 244
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1245187942"
variation 246
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:374928479"
variation 251..253
/gene="SEMA4G"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:1403173110"
variation 252
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1275021095"
variation 253
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:901912633"
variation 255
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1481477901"
variation 257
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:530008571"
variation 261
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1327288610"
variation 264
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1249370017"
variation 265
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1448212630"
variation 267
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1312036890"
variation 268
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850580770"
variation 271
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:972038592"
variation 272..277
/gene="SEMA4G"
/replace="ggcggg"
/replace="ggcgggcggg"
/db_xref="dbSNP:1850580971"
variation 279
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1026051483"
variation 281..284
/gene="SEMA4G"
/replace="g"
/replace="gaag"
/db_xref="dbSNP:1382889823"
variation 281
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:951436657"
variation 285..289
/gene="SEMA4G"
/replace="gag"
/replace="gagag"
/db_xref="dbSNP:1443272965"
variation 285
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1450869984"
variation 287
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1273406748"
variation 289
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850581596"
variation 295
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1163482462"
variation 296
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850581777"
variation 298
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:530175377"
variation 299
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1231401511"
variation 304
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850582171"
variation 319
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850582255"
variation 321
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1463848767"
exon 322..829
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 326
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1030762196"
variation 327
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850663596"
variation 331
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850663843"
variation 333
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850663913"
variation 334
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:557949623"
variation 346
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1335694004"
variation 349
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1457386306"
variation 350
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850664129"
variation 357
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1365050521"
variation 358
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850664254"
variation 359
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:892265119"
variation 360
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:570166640"
variation 361
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1414497874"
variation 362
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:867026643"
variation 363
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1394108765"
variation 364
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850664603"
variation 365
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:943019392"
variation 366
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:761543704"
variation 370
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1589978234"
variation 375
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:537435528"
variation 381
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:60278872"
variation 383
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:111933864"
variation 385
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1262698358"
variation 386
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850665019"
variation 387
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850665075"
variation 392
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1850665124"
variation 399
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1213813489"
variation 404
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850665221"
variation 411
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1316377096"
variation 414
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:980739677"
variation 418
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:182450988"
variation 419
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850665375"
variation 420
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850665422"
variation 421
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1589978258"
variation 423
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1034747287"
variation 425
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1449004233"
variation 428
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1589978265"
variation 433
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850665683"
variation 436
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1381078635"
variation 440
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850665781"
variation 442
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:934446804"
variation 444
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:960088474"
variation 449
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850665939"
variation 451..452
/gene="SEMA4G"
/replace=""
/replace="gtg"
/db_xref="dbSNP:1850666070"
variation 451
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:115583289"
variation 452
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850666120"
variation 453
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1386772616"
variation 456
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1850666516"
variation 467..471
/gene="SEMA4G"
/replace="ct"
/replace="cttct"
/db_xref="dbSNP:1330691442"
variation 475
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850666602"
variation 479
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850666651"
variation 484..487
/gene="SEMA4G"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:771249674"
variation 487
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1286727183"
variation 490
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1234279287"
variation 492
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850666856"
variation 494
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850666906"
variation 500
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:747642385"
variation 502
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1850667028"
variation 505..507
/gene="SEMA4G"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1365607676"
variation 514
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1850667141"
variation 515
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:553501059"
variation 518
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850667233"
variation 521..526
/gene="SEMA4G"
/replace="ccccc"
/replace="cccccc"
/replace="ccccccc"
/db_xref="dbSNP:1276939230"
variation 521
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850667277"
variation 522
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:578092859"
variation 526
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:949932767"
variation 527
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1044290858"
variation 531
/gene="SEMA4G"
/replace="c"
/replace="ctgc"
/db_xref="dbSNP:1850667555"
variation 537..542
/gene="SEMA4G"
/replace="cccccc"
/replace="ccccccc"
/db_xref="dbSNP:1198554590"
variation 537
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1259348483"
variation 538
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1485595178"
variation 540
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:186703368"
variation 543
/gene="SEMA4G"
/replace=""
/replace="a"
/db_xref="dbSNP:1850667867"
variation 543
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:973566758"
variation 544
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1207497990"
variation 546
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1358003866"
variation 551
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850668057"
variation 552
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1807570131"
variation 552
/gene="SEMA4G"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1807570306"
variation 558
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850668128"
variation 559
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850668209"
variation 562
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850668271"
variation 565
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1266084809"
variation 571
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1451781054"
variation 576
/gene="SEMA4G"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1328543428"
variation 576
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1293029193"
variation 578
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1381265281"
variation 580
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1345600213"
variation 582
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850668683"
variation 583
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850668734"
variation 584
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1304369840"
variation 587
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:905793660"
variation 588
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850668844"
variation 597
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:560469443"
variation 602
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850668946"
variation 603
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:563225955"
variation 606
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850669047"
variation 612
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850669092"
variation 614
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1364956082"
variation 617
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1168394557"
variation 619
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:1850669406"
variation 619
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:771649939"
variation 624
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1371109660"
variation 626
/gene="SEMA4G"
/replace=""
/replace="g"
/db_xref="dbSNP:1850669696"
variation 628
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1191340004"
variation 629
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1050718409"
variation 634
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1477407403"
variation 638
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:890089013"
variation 639
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850670117"
variation 641
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1016975985"
variation 642
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1442004696"
variation 643
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1269856612"
variation 644
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850670356"
variation 647
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:897234872"
variation 649
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:944394849"
variation 650
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1268862242"
variation 651
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1052574006"
variation 659
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:192621867"
variation 661
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:752393071"
variation 663
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1564791838"
variation 664
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850671019"
variation 666
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850671101"
variation 667..669
/gene="SEMA4G"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1850671316"
variation 667
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1224898784"
variation 669
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:867629405"
variation 671
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1250557337"
variation 673..677
/gene="SEMA4G"
/replace="ggggg"
/replace="gggggg"
/db_xref="dbSNP:1345238361"
variation 673
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:758309995"
variation 674
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:777690359"
variation 676..678
/gene="SEMA4G"
/replace="ggt"
/replace="ggtggt"
/db_xref="dbSNP:1850671886"
variation 677
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:746967585"
variation 679
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:770865272"
variation 680..681
/gene="SEMA4G"
/replace=""
/replace="tt"
/db_xref="dbSNP:1850672187"
variation 680
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:781140045"
variation 687
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1010644581"
variation 693
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1430821467"
variation 697
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850672377"
variation 702
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1402602510"
misc_feature 706..3222
/gene="SEMA4G"
/inference="COORDINATES:
alignment:Blast2seq::RefSeq|NM_001393925.1"
/note="primary ORF has stop codon >50 nucleotides from the
terminal splice site; nonsense-mediated decay (NMD)
candidate"
variation 706
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1191397762"
variation 708
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1344292943"
variation 709..732
/gene="SEMA4G"
/replace=""
/replace="tgggggaggctctggcccctcctc"
/db_xref="dbSNP:1564791884"
variation 710..714
/gene="SEMA4G"
/replace="ggggg"
/replace="gggggg"
/db_xref="dbSNP:1850672932"
variation 710
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:745907076"
variation 711
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:769754047"
variation 714
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850673074"
variation 720
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1393022504"
variation 723
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:775751808"
variation 725
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1043525758"
variation 726
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1167174298"
variation 735
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850673445"
variation 740
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:1850673633"
variation 740
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:763127413"
variation 744
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:141766082"
variation 745
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1850673834"
variation 746
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1469347701"
variation 748
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:201769907"
variation 749
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1363910803"
variation 751
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850674227"
variation 752
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:762257142"
variation 754
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850674430"
variation 755
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:768000743"
variation 756
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:753300939"
variation 757
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:765633702"
variation 759
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:528334576"
variation 767
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:764810125"
variation 768
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1322465491"
variation 770
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:752448070"
variation 773
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1261974981"
variation 775
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:150563616"
variation 776
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:751304450"
variation 777
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133857417"
variation 778
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850675630"
variation 781
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1195652118"
variation 782
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:139918504"
variation 783
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:571547734"
variation 784
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850676089"
variation 787
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850676178"
variation 790
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1202124518"
variation 792
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133857469"
variation 795
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:532192623"
variation 796
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:780081656"
variation 798
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:2133857483"
variation 800
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:867204232"
variation 801
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1159955320"
variation 808
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:749532175"
variation 809
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:768824226"
variation 812
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1850677171"
variation 814
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850677263"
variation 817
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:774700812"
variation 820
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:369789414"
variation 823
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:962113918"
variation 824..827
/gene="SEMA4G"
/replace="a"
/replace="atga"
/db_xref="dbSNP:1406530664"
variation 824
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:772310279"
variation 825
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1344402684"
variation 826
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378220105"
variation 827
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133857555"
exon 830..978
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 836
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:369353258"
variation 843
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:144341151"
variation 844
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:372839640"
variation 845
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1370809407"
variation 847
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:780136613"
variation 853
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:913597081"
variation 856
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:749297787"
variation 859
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1441420061"
variation 863
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:755205395"
variation 864
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850682502"
variation 867
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1360751746"
variation 873
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850682665"
variation 875
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1248834281"
variation 877
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850682797"
variation 878
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850682873"
variation 879
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1284517077"
variation 880
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:779253360"
variation 883
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:748287481"
variation 885
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1205748549"
variation 888..895
/gene="SEMA4G"
/replace="ggagg"
/replace="ggaggagg"
/db_xref="dbSNP:1850683258"
variation 889
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1234802535"
variation 892
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:199970914"
variation 894
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:756103359"
variation 899
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:747581175"
variation 903
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850683769"
variation 906
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1029721556"
variation 910
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1243856800"
variation 912
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1446315165"
variation 917
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:376810147"
variation 918
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1384733681"
variation 919
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1384572205"
variation 922
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:750643700"
variation 923
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:202147105"
variation 926
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1007038634"
variation 927
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1589978805"
variation 929
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1352343381"
variation 930
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1402573417"
variation 935..942
/gene="SEMA4G"
/replace="tctctc"
/replace="tctctctc"
/db_xref="dbSNP:1441071018"
variation 937
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850685194"
variation 938
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:199688982"
variation 940
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850685355"
variation 944
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:762606692"
variation 951
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:146573432"
variation 952
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:140040145"
variation 960
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1445693261"
variation 963
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850685679"
variation 965
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:761353685"
variation 966
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1387484882"
variation 967
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1056746530"
variation 971
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:373053309"
variation 974
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:750147136"
variation 976
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:760612775"
exon 979..1041
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 984
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:765388169"
variation 985
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1385079315"
variation 991
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:200094625"
variation 993
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:879452513"
variation 994
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:752650927"
variation 995..998
/gene="SEMA4G"
/replace="c"
/replace="cccc"
/db_xref="dbSNP:1589979126"
variation 996
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:149776999"
variation 999
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:891205288"
variation 1002
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1423146487"
variation 1006
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850694572"
variation 1012..1014
/gene="SEMA4G"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1457139894"
variation 1012
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1257694646"
variation 1017
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:751823274"
variation 1020
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1224318002"
variation 1022..1026
/gene="SEMA4G"
/replace="aaaaa"
/replace="aaaaaa"
/db_xref="dbSNP:769978574"
variation 1022
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:757731950"
variation 1023
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:368462093"
variation 1030
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1221941297"
variation 1035
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1274539366"
variation 1037
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:746403415"
variation 1039
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1056293944"
exon 1042..1140
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 1042
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1433192968"
variation 1043
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:374837913"
variation 1044..1045
/gene="SEMA4G"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1564794259"
variation 1044
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:368885285"
variation 1047
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1488741560"
variation 1050
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850858994"
variation 1055
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:759972554"
variation 1056
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1311071149"
variation 1057
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:765790226"
variation 1059
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:371741444"
variation 1060
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:756797401"
variation 1062
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:941992758"
variation 1063
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:145690277"
variation 1064
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:750061929"
variation 1065
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850859667"
variation 1066
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564794293"
variation 1071
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850859891"
variation 1073
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1259506525"
variation 1074
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:560293126"
variation 1075..1085
/gene="SEMA4G"
/replace="c"
/replace="cggctcaattc"
/db_xref="dbSNP:1850860190"
variation 1075
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:893274055"
variation 1076
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:749056930"
variation 1077
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1370695015"
variation 1081
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:768561807"
variation 1087
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:779061181"
variation 1089
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1432659738"
variation 1091
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1589984551"
variation 1092
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:921297403"
variation 1093
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850860820"
variation 1095
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:748069351"
variation 1098
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850860959"
variation 1099
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:376189318"
variation 1103
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:932716016"
variation 1105
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:751439655"
variation 1107
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:772327550"
variation 1112
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:572662465"
variation 1113
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:760573069"
variation 1114
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1406589169"
variation 1116
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850861612"
variation 1118
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1300897600"
variation 1120
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133871074"
variation 1122
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850861780"
variation 1123
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1295606625"
variation 1125
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1413321602"
variation 1126..1129
/gene="SEMA4G"
/replace="ct"
/replace="ctct"
/db_xref="dbSNP:1438510738"
variation 1126
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1366536028"
variation 1128
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850862143"
variation 1131
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1400263197"
variation 1136
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1340182509"
variation 1137..1138
/gene="SEMA4G"
/replace="ca"
/replace="caca"
/db_xref="dbSNP:764948073"
variation 1138
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850862460"
variation 1139
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850862536"
exon 1141..1234
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 1141
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1004659697"
variation 1143
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1205461904"
variation 1149
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:746066448"
variation 1150
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:770161568"
variation 1151
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:149008935"
variation 1157
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:764608308"
variation 1161
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1446373763"
variation 1166
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:887525390"
variation 1168
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133873792"
variation 1169
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:151095552"
variation 1170
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:963256942"
variation 1172
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:774709885"
variation 1173
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:74154244"
variation 1174
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:779530961"
variation 1178
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:748582901"
variation 1179
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:753596253"
variation 1180
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1362954670"
variation 1181
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1336829326"
variation 1184..1188
/gene="SEMA4G"
/replace="ag"
/replace="aggag"
/db_xref="dbSNP:768692347"
variation 1185
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:374443024"
variation 1186
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:752480989"
variation 1188
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:758114685"
variation 1190
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1215594471"
variation 1192
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1564794890"
variation 1193
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:758664453"
variation 1198
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1326652882"
variation 1200
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1316309086"
variation 1201
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1198014436"
variation 1208
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:746889193"
variation 1210
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:140978394"
variation 1211
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:201619012"
variation 1213
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1589985904"
variation 1214
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1236872889"
variation 1217
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:934729093"
variation 1222
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850892374"
variation 1223
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850892457"
variation 1227
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:746116241"
variation 1228
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1420941687"
variation 1229
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1477311108"
variation 1231
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:769933802"
variation 1233
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:775849846"
exon 1235..1348
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 1235
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1242205501"
variation 1236
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850902998"
variation 1239
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:749483446"
variation 1240..1241
/gene="SEMA4G"
/replace="g"
/replace="gg"
/db_xref="dbSNP:750452775"
variation 1240
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:769114862"
variation 1241
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1444498751"
variation 1242
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:948989926"
variation 1243
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1352712085"
variation 1244
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1850903953"
variation 1249
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:202220509"
variation 1250
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:773841551"
variation 1251
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:759183570"
variation 1252
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:769395836"
variation 1259
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:775330142"
variation 1262
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:762461498"
variation 1270
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:370387075"
variation 1271
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:751241762"
variation 1274
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1419465318"
variation 1276..1278
/gene="SEMA4G"
/replace="att"
/replace="attatt"
/db_xref="dbSNP:760677059"
variation 1277
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564795185"
variation 1278
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1589986519"
variation 1285
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1393099586"
variation 1286
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1589986527"
variation 1287..1300
/gene="SEMA4G"
/replace="ccgcc"
/replace="ccgccggagccgcc"
/db_xref="dbSNP:1392548033"
variation 1288
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:188609242"
variation 1289
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:375357185"
variation 1291
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:200186312"
variation 1292
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:756229401"
variation 1294
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1375680753"
variation 1295
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850905942"
variation 1297
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:534321099"
variation 1298
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:780089392"
variation 1300
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:374506045"
variation 1302
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1850906271"
variation 1303
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1159156117"
variation 1306
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:759497574"
variation 1307
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1246356373"
variation 1308
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:554197284"
variation 1310
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:142527271"
variation 1312..1313
/gene="SEMA4G"
/replace=""
/replace="ct"
/db_xref="dbSNP:765930905"
variation 1314
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:192790321"
variation 1320
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:753223422"
variation 1320
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133875208"
variation 1321..1326
/gene="SEMA4G"
/replace="gag"
/replace="gaggag"
/db_xref="dbSNP:1439037196"
variation 1323
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:755117958"
variation 1331
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:779341258"
variation 1332
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1181223858"
variation 1333
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1439657511"
variation 1336
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:954618111"
variation 1338
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1184542680"
variation 1345
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:748404181"
exon 1349..1518
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 1350
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:374767509"
variation 1352
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:369471768"
variation 1353
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:145899563"
variation 1355
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1319299438"
variation 1356
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:768211235"
variation 1361
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1461931758"
variation 1362
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1392770440"
variation 1368
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:562278554"
variation 1369
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:138710515"
variation 1374
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:772951663"
variation 1375
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:528948930"
variation 1378
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:760610802"
variation 1379
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:371666695"
variation 1380
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1178341036"
variation 1381
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1303651661"
variation 1385
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1208157981"
variation 1386
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:907505061"
variation 1389
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1316488117"
variation 1390
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:759573797"
variation 1396
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1465509378"
variation 1398
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:765335147"
variation 1399
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1452714855"
variation 1402
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1292595629"
variation 1407
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:752884133"
variation 1408
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:758650850"
variation 1410
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:940372860"
variation 1411..1413
/gene="SEMA4G"
/replace=""
/replace="gac"
/db_xref="dbSNP:1850922975"
variation 1414
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1297186803"
variation 1416
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1037811860"
variation 1421
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1356018019"
variation 1423
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1387941598"
variation 1425..1431
/gene="SEMA4G"
/replace="cttc"
/replace="cttcttc"
/db_xref="dbSNP:1298602317"
variation 1427
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1329808982"
variation 1428
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1233131910"
variation 1431
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:751912530"
variation 1433
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:540792779"
variation 1434
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:781655724"
variation 1438
/gene="SEMA4G"
/replace=""
/replace="c"
/db_xref="dbSNP:781528969"
variation 1438
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:898907623"
variation 1439
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:775552640"
variation 1446
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:754499823"
variation 1450
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:199950454"
variation 1452
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:142733326"
variation 1454
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850925211"
variation 1458
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133876712"
variation 1460
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1179175680"
variation 1462
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:771647101"
variation 1470
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1382158574"
variation 1471
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850925617"
variation 1477
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:773006606"
variation 1478
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:201790937"
variation 1480
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850926055"
variation 1482
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:919007889"
variation 1488..1505
/gene="SEMA4G"
/replace="ccgtgtggc"
/replace="ccgtgtggcccgtgtggc"
/db_xref="dbSNP:746431273"
variation 1488
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:868505946"
variation 1489
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:770726629"
variation 1490
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:551004768"
variation 1492
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1389345205"
variation 1493
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:759469028"
variation 1498..1511
/gene="SEMA4G"
/replace="cgtgtggctcgtgt"
/replace="cgtgtggctcgtgtggctcgtgt"
/db_xref="dbSNP:1850927374"
variation 1498
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:765262844"
variation 1499
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:377151700"
variation 1500
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:763278051"
variation 1503
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:764466706"
variation 1504
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:751824969"
variation 1507
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:888912092"
variation 1508
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1224011022"
variation 1509
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:118166648"
variation 1511
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:767904665"
variation 1517
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1850928191"
variation 1518
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1199366181"
exon 1519..1688
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 1519
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:2133877724"
variation 1520
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:200202967"
variation 1522
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:762050264"
variation 1524
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1170863177"
variation 1525
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133877770"
variation 1526
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:137857983"
variation 1527..1529
/gene="SEMA4G"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1850933595"
variation 1529
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:866490784"
variation 1531
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133877805"
variation 1532
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133877813"
variation 1533
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850933809"
variation 1535
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133877834"
variation 1536
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1238045368"
variation 1537
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133877862"
variation 1539
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:961966703"
variation 1540
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133877885"
variation 1542
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133877896"
variation 1544
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:1850934122"
variation 1544
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133877909"
variation 1546
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133877929"
variation 1547..1554
/gene="SEMA4G"
/replace="agaag"
/replace="agaagaag"
/db_xref="dbSNP:1179910574"
variation 1547
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133877937"
variation 1548
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:750733650"
variation 1549
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133877972"
variation 1550
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1850934544"
variation 1551
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:149549143"
variation 1552
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1850934768"
variation 1553
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133878008"
variation 1554
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:766970037"
variation 1555
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133878023"
variation 1556
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133878031"
variation 1559
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133878041"
variation 1560
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:144136150"
variation 1561
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133878063"
variation 1563
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133878069"
variation 1564
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850935025"
variation 1565
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:2133878084"
variation 1567
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133878090"
variation 1570
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133878099"
variation 1573
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:2133878106"
variation 1574
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133878118"
variation 1576
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:954409603"
variation 1577
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:374601814"
variation 1579
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:908122906"
variation 1581
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133878155"
variation 1582
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1329807522"
variation 1586
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133878172"
variation 1587
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564795878"
variation 1588
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133878196"
variation 1589
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:777213392"
variation 1590
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:751242836"
variation 1592
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133878218"
variation 1593
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133878227"
variation 1595
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133878231"
variation 1596
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:188155769"
variation 1598
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:138709087"
variation 1600
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:780858350"
variation 1601
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:141723515"
variation 1605
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:2133878282"
variation 1606
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850935891"
variation 1607
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:201040570"
variation 1608
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:200499542"
variation 1611
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1372311283"
variation 1612
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:576159833"
variation 1613
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:376301016"
variation 1617
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1413942825"
variation 1622
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850936462"
variation 1628
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:774536639"
variation 1632
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1313882295"
variation 1635
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1207707838"
variation 1639
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:943187702"
variation 1645
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:767392247"
variation 1646
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1161933809"
variation 1647
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:761950373"
variation 1648
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:772280066"
variation 1649
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:749963260"
variation 1650
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1235341225"
variation 1652
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:761169377"
variation 1654
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:766701174"
variation 1656
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:754363609"
variation 1657
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850937754"
variation 1660
/gene="SEMA4G"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1426443730"
variation 1662
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:759995340"
variation 1663
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:370799129"
variation 1673
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:755545765"
variation 1674
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:374213077"
variation 1675
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1420759299"
variation 1677
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1313225853"
variation 1678
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133878596"
variation 1680
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133878605"
variation 1681
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133878615"
variation 1683
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:146235728"
variation 1687
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:767264493"
exon 1689..1833
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 1689
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1473090285"
variation 1691
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:184755985"
variation 1693
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1589989813"
variation 1694
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:142303289"
variation 1695
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413764190"
variation 1696
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:200241224"
variation 1700
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1850976356"
variation 1702
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:764921000"
variation 1703
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1216318709"
variation 1704
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:752708818"
variation 1709
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:758200614"
variation 1711
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1161211887"
variation 1715
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1201341797"
variation 1717
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:369063086"
variation 1718
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:751695050"
variation 1720
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850977775"
variation 1721
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1187494537"
variation 1723
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1589989912"
variation 1726
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850978202"
variation 1729
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1264248737"
variation 1730
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1589989925"
variation 1734
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:964354750"
variation 1735
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1850978747"
variation 1740
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:190271357"
variation 1741
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1372385660"
variation 1743
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:757320010"
variation 1745
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:376797424"
variation 1746
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850979346"
variation 1747
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:150824972"
variation 1748
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1240413142"
variation 1749
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1193173688"
variation 1751
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1399753855"
variation 1754
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850979819"
variation 1755
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1433937750"
variation 1756..1758
/gene="SEMA4G"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1452660752"
variation 1756
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:780443579"
variation 1758
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:367883776"
variation 1761
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:770163597"
variation 1763
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1342003827"
variation 1771
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1397546136"
variation 1772
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:372466257"
variation 1773
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850980546"
variation 1774
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:749809765"
variation 1776
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:376969087"
variation 1778
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850980816"
variation 1780
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1229991911"
variation 1781..1783
/gene="SEMA4G"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:35989286"
variation 1781
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1339531318"
variation 1783
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:988692457"
variation 1784
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:774913495"
variation 1786
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:199762950"
variation 1787
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:553537753"
variation 1790
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850981685"
variation 1791
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:776474084"
variation 1793
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:759217416"
variation 1795
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1261099304"
variation 1796
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:199677082"
variation 1798
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1200907162"
variation 1799
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:752375155"
variation 1803
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:577628245"
variation 1805
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:764005138"
variation 1806
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:751463430"
variation 1807
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:781196938"
variation 1809
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:750677818"
variation 1810
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1390825588"
variation 1812
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1388071510"
variation 1814
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850983227"
variation 1815
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:756226933"
variation 1816
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:965691185"
variation 1821
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1365199089"
variation 1822
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:949989449"
variation 1823
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:147630038"
variation 1832
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:749676557"
variation 1833
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:768865327"
exon 1834..2056
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 1834
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:775053317"
variation 1843
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850994061"
variation 1845..1846
/gene="SEMA4G"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1564796771"
variation 1847
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1850994366"
variation 1850
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:748920327"
variation 1852
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:761554973"
variation 1853
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:774063487"
variation 1857
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850994826"
variation 1858
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:761753573"
variation 1868
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:917222193"
variation 1873
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1850995253"
variation 1875
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1210217429"
variation 1876
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1354888744"
variation 1877
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1564796809"
variation 1878..1884
/gene="SEMA4G"
/replace=""
/replace="agacttg"
/db_xref="dbSNP:1564796818"
variation 1879
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:767502487"
variation 1881
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:773129383"
variation 1884
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:760713409"
variation 1885
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1203491941"
variation 1886
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:766463475"
variation 1892
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850996705"
variation 1893
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1471143694"
variation 1894
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:754033511"
variation 1895
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850996981"
variation 1897
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1290463761"
variation 1899
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:755190563"
variation 1902
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:765708793"
variation 1908
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:971229127"
variation 1911..1939
/gene="SEMA4G"
/replace="gttg"
/replace="gttgcacccactgatggctcggcccgttg"
/db_xref="dbSNP:1850997601"
variation 1912
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:753167511"
variation 1915
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:979985262"
variation 1917
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1221818105"
variation 1918
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1371460605"
variation 1919..1922
/gene="SEMA4G"
/replace=""
/replace="cact"
/db_xref="dbSNP:1422220691"
variation 1920
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:758828192"
variation 1921
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:778460071"
variation 1928
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850998242"
variation 1929
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1170412118"
variation 1930
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1330018610"
variation 1931
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:199635372"
variation 1934
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:779575501"
variation 1935
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:565104337"
variation 1936
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:201564489"
variation 1937
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1400651750"
variation 1938
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850999005"
variation 1939
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:778525725"
variation 1941
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:748004748"
variation 1942
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1213885536"
variation 1948
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:149116714"
variation 1949
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:371636173"
variation 1954
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:367801117"
variation 1955
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:770950663"
variation 1956
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1589990995"
variation 1959
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:889294061"
variation 1965
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1182151325"
variation 1969
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:776709167"
variation 1972
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:759518723"
variation 1973
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:76584327"
variation 1976
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:143118773"
variation 1978
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1186433901"
variation 1981
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:150071842"
variation 1982
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:764503702"
variation 1987
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851000938"
variation 1989
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1345529789"
variation 1990
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:752037569"
variation 1991
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133884735"
variation 1993
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851001443"
variation 1995
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:757714467"
variation 1997
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:779441290"
variation 1998
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1316183503"
variation 2007
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851001826"
variation 2009
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851001929"
variation 2010..2015
/gene="SEMA4G"
/replace="cac"
/replace="caccac"
/db_xref="dbSNP:755502387"
variation 2015
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:147741050"
variation 2016
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851002277"
variation 2028
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:199671205"
variation 2030
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:553260640"
variation 2032
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:1851002597"
variation 2033
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:747781429"
variation 2038
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1231751585"
variation 2039
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1457264028"
variation 2040
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1564797032"
variation 2041
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851003219"
variation 2043
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133884897"
variation 2046
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564797037"
variation 2047
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:771880296"
variation 2049
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851003533"
variation 2053
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1354200251"
exon 2057..2172
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 2057
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851018889"
variation 2058
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:750865022"
variation 2063
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:754532026"
variation 2068
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1302211133"
variation 2070
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1564797210"
variation 2073
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1458448137"
variation 2075
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:201540929"
variation 2076
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:752382102"
variation 2079
/gene="SEMA4G"
/replace="c"
/replace="cctac"
/db_xref="dbSNP:1851020664"
variation 2079
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:7901675"
variation 2080
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:144844358"
variation 2084
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1427873810"
variation 2085
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:542169408"
variation 2086
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:781235374"
variation 2088
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:200666280"
variation 2089
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1400944443"
variation 2090
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1425740385"
variation 2093
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564797257"
variation 2096
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:770024953"
variation 2097
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:775644707"
variation 2100
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:147919269"
variation 2101
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851022799"
variation 2103
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1735148329"
variation 2108
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:372822376"
variation 2111
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:962692236"
variation 2115
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:377379944"
variation 2118
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133886261"
variation 2119
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851023312"
variation 2120
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:762280561"
variation 2123
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1009845265"
variation 2124
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851023747"
variation 2127
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:767751429"
variation 2128
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1384559788"
variation 2130
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:773734788"
variation 2133
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1340727081"
variation 2134
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133886347"
variation 2136
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1661076286"
variation 2137
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1253166327"
variation 2139
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1197875859"
variation 2140
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:761134082"
variation 2142..2145
/gene="SEMA4G"
/replace="tg"
/replace="tgtg"
/db_xref="dbSNP:1851024692"
variation 2143
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1437655804"
variation 2144
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:764733748"
variation 2145
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:752147128"
variation 2156
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:757896884"
variation 2158
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1307458129"
variation 2159..2165
/gene="SEMA4G"
/replace="tctct"
/replace="tctctct"
/db_xref="dbSNP:1187347525"
variation 2159
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1424188963"
variation 2166
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:763844803"
variation 2167
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:377270509"
variation 2172
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1395507326"
exon 2173..2333
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 2174
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:200163492"
variation 2175
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:773503586"
variation 2176
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1316773436"
variation 2178
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:761187011"
variation 2182
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1235416443"
variation 2184
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1306051543"
variation 2187
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:766932360"
variation 2188
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1353345900"
variation 2189
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:777088467"
variation 2191
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1191733049"
variation 2192
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1261588998"
variation 2194
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:762570919"
variation 2195
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1203475590"
variation 2197
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:763459869"
variation 2199
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:141233234"
variation 2200
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:778175945"
variation 2203
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851035626"
variation 2206
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:113498503"
variation 2208
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1453643880"
variation 2211
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133887370"
variation 2216
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:755967370"
variation 2219
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1367220882"
variation 2220
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:200695967"
variation 2223
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851036004"
variation 2229
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1365187139"
variation 2230
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1450944219"
variation 2231
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:962865221"
variation 2233
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:780182850"
variation 2234
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:147992447"
variation 2235
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1453337360"
variation 2239
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:140692272"
variation 2240
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:778822733"
variation 2242
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133887521"
variation 2248
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851036845"
variation 2252
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1328594140"
variation 2253
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1564797582"
variation 2258
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1442804873"
variation 2260
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:748411182"
variation 2261
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851037376"
variation 2264
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851037479"
variation 2266
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:772130257"
variation 2267
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1307898484"
variation 2272
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1449228698"
variation 2274
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:770900988"
variation 2276
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851038019"
variation 2277
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1318990634"
variation 2279
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1236915123"
variation 2282
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1260199125"
variation 2284
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851038517"
variation 2285
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851038668"
variation 2286
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:777961396"
variation 2288
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:747411614"
variation 2289
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1251127577"
variation 2290
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1382570602"
variation 2292
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:771261070"
variation 2293
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:371386076"
variation 2297
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:756576170"
variation 2298
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:759917226"
variation 2300
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:768215640"
variation 2302
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1180693559"
variation 2303
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1417942007"
variation 2307
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:780011724"
variation 2308
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:761371562"
variation 2310
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133887829"
variation 2311
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1392930732"
variation 2314
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851041113"
variation 2315
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1461216948"
variation 2321
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:767343866"
variation 2322
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:750070570"
variation 2323
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1389861288"
variation 2325
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1229597463"
variation 2327
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:760597640"
variation 2328
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:912639818"
variation 2329
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:984794076"
variation 2333
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:766227835"
exon 2334..2395
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 2334
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851052204"
variation 2337
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:138772734"
variation 2340
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851052415"
variation 2341
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:375633368"
variation 2342
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1358635527"
variation 2343..2359
/gene="SEMA4G"
/replace="ga"
/replace="gatacaggacatagaga"
/db_xref="dbSNP:1435619713"
variation 2345
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1271640141"
variation 2348
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:764114736"
variation 2349
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:995770723"
variation 2354
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851053214"
variation 2355..2362
/gene="SEMA4G"
/replace="agag"
/replace="agagagag"
/db_xref="dbSNP:767881320"
variation 2356
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1325570015"
variation 2358
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:190201835"
variation 2359
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851053643"
variation 2361
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851053737"
variation 2367
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:538842540"
variation 2368
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851053925"
variation 2369
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:757411949"
variation 2373
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133889080"
variation 2377
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:781378063"
variation 2378
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:746282456"
variation 2380
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1231622802"
variation 2381
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1279237287"
variation 2383
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:756467836"
variation 2385
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:369529769"
variation 2388
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851054882"
variation 2390
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:534283434"
exon 2396..3448
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 2396
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1373085610"
variation 2397
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851211935"
variation 2398..2410
/gene="SEMA4G"
/replace="ccaccaccac"
/replace="ccaccaccaccac"
/replace="ccaccaccaccaccac"
/db_xref="dbSNP:145835827"
variation 2398..2399
/gene="SEMA4G"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1554884798"
variation 2400
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1334008977"
variation 2404
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1327563265"
variation 2406
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851212995"
variation 2410..2412
/gene="SEMA4G"
/replace=""
/replace="ctg"
/db_xref="dbSNP:755081302"
variation 2414
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:552270687"
variation 2417
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1341977736"
variation 2418
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1235282106"
variation 2419
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1282755788"
variation 2420
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:754085049"
variation 2425
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1589998314"
variation 2428
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1199969523"
variation 2431
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:760031264"
variation 2432
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:753257306"
variation 2434
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133901396"
variation 2435
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:773478369"
variation 2436
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:778125924"
variation 2441
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:570573396"
variation 2443
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1175068535"
variation 2448
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:755545892"
variation 2451
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:779730408"
variation 2453
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1158667773"
variation 2456
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:748889973"
variation 2457
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1384413039"
variation 2460
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:768472015"
variation 2461
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:761068926"
variation 2464
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1442105033"
variation 2465
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851217451"
variation 2466
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851217575"
variation 2468
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1305846909"
variation 2469
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:183718929"
variation 2470
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1232869244"
variation 2472
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:549851109"
variation 2475
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1245506254"
variation 2476
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1353024006"
variation 2479
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:146245319"
variation 2480
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:760851566"
variation 2481
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851218914"
variation 2482
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851219065"
variation 2484
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:770897727"
variation 2486
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1195301504"
variation 2487
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1264768450"
variation 2490
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:777019767"
variation 2492
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:759761969"
variation 2493
/gene="SEMA4G"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1005161073"
variation 2494
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:201001972"
variation 2498
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1451010139"
variation 2499
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851220823"
variation 2504
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1157499811"
variation 2506
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:776051888"
variation 2507
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851221493"
variation 2508
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1005716850"
variation 2509
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851222036"
variation 2513
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851222273"
variation 2514
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1017136365"
variation 2516
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:763219828"
variation 2517
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:764701072"
variation 2518
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:137971825"
variation 2520
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:755671543"
variation 2522
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851223790"
variation 2523
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851224022"
variation 2524
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1355476316"
variation 2525
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1589998686"
variation 2526..2528
/gene="SEMA4G"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1251708384"
variation 2526
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:977978033"
variation 2527
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:765835066"
variation 2528
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851225605"
variation 2529
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1589998724"
variation 2532
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:753494547"
variation 2533
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1315808916"
variation 2535
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1287605179"
variation 2536
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:149389232"
variation 2537
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:144727154"
variation 2538
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851227514"
variation 2541
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:748043373"
variation 2543
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851228007"
variation 2544
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:148516703"
variation 2545
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:374200198"
variation 2547
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851228915"
variation 2550
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:142773171"
variation 2551
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:147237913"
variation 2559
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851229807"
variation 2560
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:141030743"
variation 2562
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851230304"
variation 2565
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851230541"
variation 2568..2569
/gene="SEMA4G"
/replace=""
/replace="tg"
/db_xref="dbSNP:1851230987"
variation 2568
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851230778"
variation 2569
/gene="SEMA4G"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1851231197"
variation 2571
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:770205655"
variation 2574
/gene="SEMA4G"
/replace=""
/replace="g"
/db_xref="dbSNP:1851231852"
variation 2574
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851231625"
variation 2575..2576
/gene="SEMA4G"
/replace=""
/replace="aa"
/db_xref="dbSNP:1851232419"
variation 2575
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:775542275"
variation 2576
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851232649"
variation 2577
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851232858"
variation 2578
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851233038"
variation 2578
/gene="SEMA4G"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1851233269"
variation 2580
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851233489"
variation 2589
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:755113434"
variation 2590
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:764316566"
variation 2595
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:774952582"
variation 2598
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133902664"
variation 2601
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:762161081"
variation 2603
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1298897763"
variation 2606
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851235035"
variation 2607
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:765887043"
variation 2608
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:753406520"
variation 2609
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1408024389"
variation 2613
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851235974"
variation 2616
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:754482102"
variation 2617
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1307475986"
variation 2619
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:764912089"
variation 2620
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:539263557"
variation 2621
/gene="SEMA4G"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1851237219"
variation 2623
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:866091256"
variation 2624
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:558586100"
variation 2625
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:777395006"
variation 2626
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1589998968"
variation 2627
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851238350"
variation 2628
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851238569"
variation 2629
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1049622681"
variation 2630
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:746976668"
variation 2631
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:940882437"
variation 2637
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:757318232"
variation 2640
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851239938"
variation 2642
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851240164"
variation 2643
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1444392472"
variation 2645
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1204049997"
variation 2646
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851240875"
variation 2649
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:977211113"
variation 2651
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851241278"
variation 2652
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1257594428"
variation 2655
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1486401615"
variation 2656
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:781268916"
variation 2657
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:144879682"
variation 2658
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1423563944"
variation 2659
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851242706"
variation 2662
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1171588564"
variation 2664..2666
/gene="SEMA4G"
/replace="cac"
/replace="cacac"
/db_xref="dbSNP:1392472908"
variation 2667
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851243412"
variation 2671
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:902133075"
variation 2673
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851243897"
variation 2675
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851244159"
variation 2677
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851244380"
variation 2683
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851244630"
variation 2686
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1168271228"
variation 2687
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1376084022"
variation 2689
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1416703361"
variation 2692
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:775801456"
variation 2698
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1378378322"
variation 2699
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:997799025"
variation 2700
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851245990"
variation 2703
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:749431067"
variation 2704
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1339881664"
variation 2708
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1031887205"
variation 2710
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:769068051"
variation 2712
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1589999247"
variation 2713
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:774521972"
variation 2714
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1207455851"
variation 2715
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:762152467"
variation 2716
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:772635727"
variation 2717
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851247954"
variation 2718..2722
/gene="SEMA4G"
/replace="tg"
/replace="tgatg"
/db_xref="dbSNP:1187659489"
variation 2718
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851248197"
variation 2719
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851248500"
variation 2721
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851248659"
variation 2722
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:957195278"
variation 2727
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1589999321"
variation 2728
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851249179"
variation 2729
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:759100020"
variation 2730
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1448113201"
variation 2731
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851249681"
variation 2732
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:990022918"
variation 2734
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1395953506"
variation 2735
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:544195173"
variation 2736
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851250291"
variation 2738
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:752430522"
variation 2740
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1358691563"
variation 2745
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1224493460"
variation 2749
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1454241106"
variation 2750
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1265325492"
variation 2751..2755
/gene="SEMA4G"
/replace="c"
/replace="cgcgc"
/db_xref="dbSNP:1851251239"
variation 2751
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:147942823"
variation 2752
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:140546736"
variation 2753
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:751374543"
variation 2754..2755
/gene="SEMA4G"
/replace=""
/replace="tata"
/db_xref="dbSNP:1851251846"
variation 2754
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:757083877"
variation 2757
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1589999484"
variation 2758
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:149914326"
variation 2759
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:750335846"
variation 2768..2783
/gene="SEMA4G"
/replace="gcctcatcctggcctc"
/replace="gcctcatcctggcctcatcctggcctc"
/db_xref="dbSNP:1851252713"
variation 2768
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1380369416"
variation 2770
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:756293264"
variation 2772
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:779930213"
variation 2776
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851253195"
variation 2780
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:939406010"
variation 2781
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:749539011"
variation 2782
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1270578063"
variation 2783
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:71488078"
variation 2784
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851254045"
variation 2786
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:768819125"
variation 2788
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:144937502"
variation 2792..2794
/gene="SEMA4G"
/replace=""
/replace="tct"
/db_xref="dbSNP:569204913"
variation 2795
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:748554644"
variation 2796
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851254882"
variation 2797
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1210510722"
variation 2800
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:887229636"
variation 2801
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:772406976"
variation 2802
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851255424"
variation 2808
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851255543"
variation 2809
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:773734595"
variation 2810
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:761134134"
variation 2813
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851256014"
variation 2815
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:769355889"
variation 2816
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:774916385"
variation 2821
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:542184127"
variation 2822
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1326312908"
variation 2823
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851256871"
variation 2825
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:763691852"
variation 2826
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851257157"
variation 2827
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:149052530"
variation 2828
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:41291464"
variation 2829
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851257680"
variation 2830
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1242957860"
variation 2831
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:527848892"
variation 2832
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851258036"
variation 2833
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:756057332"
variation 2834
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:780027867"
variation 2835
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851258594"
variation 2837
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413539150"
variation 2839
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:200288019"
variation 2840..2846
/gene="SEMA4G"
/replace="act"
/replace="actcact"
/db_xref="dbSNP:748396129"
variation 2840
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1327673019"
variation 2843
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1208690414"
variation 2844
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851259631"
variation 2845
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1274190195"
variation 2847
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133904692"
variation 2848
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1159862173"
variation 2851
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:138505815"
variation 2852
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:140405167"
variation 2856
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851260166"
variation 2857
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1473694674"
variation 2860
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:779055594"
variation 2861
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:531476226"
variation 2863
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1286873399"
variation 2865
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:778047878"
variation 2867
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:145555722"
variation 2868..2893
/gene="SEMA4G"
/replace="ag"
/replace="aggatctgcggtgcaactgcagacag"
/db_xref="dbSNP:1351574365"
variation 2868
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1472206434"
variation 2869
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:771404491"
variation 2870
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415680566"
variation 2871
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851262875"
variation 2872
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851263063"
variation 2874
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851263236"
variation 2876
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:777161655"
variation 2877
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:138067900"
variation 2878
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1282725183"
variation 2880
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1354773723"
variation 2881
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1411329720"
variation 2883
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851264505"
variation 2885
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1305609497"
variation 2886
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851264866"
variation 2890..2892
/gene="SEMA4G"
/replace="a"
/replace="aca"
/db_xref="dbSNP:1349407594"
variation 2891
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1228303776"
variation 2892
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851265432"
variation 2893
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1285314078"
variation 2899
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1358827837"
variation 2906
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1226997498"
variation 2909
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:375760083"
variation 2912
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1438587910"
variation 2914
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:774176474"
variation 2916
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1249714433"
variation 2917
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:761489347"
variation 2918
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1188499233"
variation 2920..2939
/gene="SEMA4G"
/replace="gatgagggtgatgatgaggg"
/replace="gatgagggtgatgatgagggtgatgatgaggg"
/db_xref="dbSNP:772358119"
variation 2922
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:767433560"
variation 2923..2926
/gene="SEMA4G"
/replace="g"
/replace="gagg"
/db_xref="dbSNP:1851267553"
variation 2925
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:773199318"
variation 2926
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:760515196"
variation 2927
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1359315768"
variation 2933
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:145330425"
variation 2935
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:753794838"
variation 2935
/gene="SEMA4G"
/replace="g"
/replace="gg"
/replace="gggg"
/db_xref="dbSNP:1851268481"
variation 2936
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133905431"
variation 2937..2948
/gene="SEMA4G"
/replace="gggggctggggg"
/replace="gggggctggggggctggggg"
/db_xref="dbSNP:1406962803"
variation 2937..2941
/gene="SEMA4G"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1411362753"
variation 2937..2938
/gene="SEMA4G"
/replace=""
/replace="aa"
/db_xref="dbSNP:1851269415"
variation 2937
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:755038247"
variation 2939
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1369335681"
variation 2940
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1414869947"
variation 2941
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851270194"
variation 2942..2953
/gene="SEMA4G"
/replace="ctgggggcctgg"
/replace="ctgggggcctgggggcctgg"
/db_xref="dbSNP:1475018399"
variation 2942
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1335400856"
variation 2943
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590000321"
variation 2945
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1342807731"
variation 2948
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:565974154"
variation 2949
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590000368"
variation 2951
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1283942354"
variation 2955
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:927913032"
variation 2956
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851271928"
variation 2957
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1230873584"
variation 2958
/gene="SEMA4G"
/replace=""
/replace="c"
/db_xref="dbSNP:1487389551"
variation 2958
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851272264"
variation 2959
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851272553"
variation 2960
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1272774402"
variation 2962
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:752924036"
variation 2963
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1201126917"
variation 2964
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851273137"
variation 2967
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:539199769"
variation 2969
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:889434035"
variation 2971
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851273660"
variation 2976
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1011010207"
variation 2979
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851273972"
variation 2985
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851274114"
variation 2988
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:200801941"
variation 2989..2990
/gene="SEMA4G"
/replace=""
/replace="gc"
/replace="gccc"
/replace="gcccc"
/replace="gccccc"
/replace="gcccccc"
/replace="gccccccc"
/db_xref="dbSNP:rs1851274585"
variation 2989
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851274273"
variation 2989
/gene="SEMA4G"
/replace="g"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1554885050"
variation 2990..2994
/gene="SEMA4G"
/replace=""
/replace="cccca"
/db_xref="dbSNP:1851275324"
variation 2990..2993
/gene="SEMA4G"
/replace="ccc"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1307646381"
variation 2990
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1564800318"
variation 2991..2998
/gene="SEMA4G"
/replace="ccc"
/replace="cccagccc"
/db_xref="dbSNP:1451113011"
variation 2991
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1490149544"
variation 2992
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1319007353"
variation 2994..2995
/gene="SEMA4G"
/replace=""
/replace="ag"
/db_xref="dbSNP:1244403035"
variation 2994
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:747411482"
variation 2995
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:757616280"
variation 2995
/gene="SEMA4G"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1851276615"
variation 2996..3011
/gene="SEMA4G"
/replace="ccccacc"
/replace="ccccaccacccccacc"
/db_xref="dbSNP:1851277127"
variation 2996..2999
/gene="SEMA4G"
/replace="cccc"
/replace="ccccccccccc"
/replace="ccccccccccccccc"
/db_xref="dbSNP:1564800345"
variation 2996
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1389197846"
variation 2997
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1434747606"
variation 2999..3004
/gene="SEMA4G"
/replace="c"
/replace="caccac"
/db_xref="dbSNP:1173800017"
variation 2999
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133906339"
variation 3000..3003
/gene="SEMA4G"
/replace=""
/replace="acca"
/db_xref="dbSNP:1399486489"
variation 3000
/gene="SEMA4G"
/replace=""
/replace="a"
/db_xref="dbSNP:1851277715"
variation 3000
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1326270062"
variation 3001
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:781570245"
variation 3002
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:746344453"
variation 3003
/gene="SEMA4G"
/replace=""
/replace="a"
/db_xref="dbSNP:1851278531"
variation 3003
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1438563345"
variation 3004..3023
/gene="SEMA4G"
/replace="cccccaccgcc"
/replace="cccccaccgcccccaccgcc"
/replace="cccccaccgcccccaccgcccccaccgcc"
/db_xref="dbSNP:773176617"
variation 3004..3008
/gene="SEMA4G"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:746736051"
variation 3005
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1334155427"
variation 3006
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:570600855"
variation 3009
/gene="SEMA4G"
/replace=""
/replace="a"
/db_xref="dbSNP:1366311394"
variation 3009
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1437736186"
variation 3010
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1465984153"
variation 3011
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:537981098"
variation 3012
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1364699879"
variation 3014
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1234288227"
variation 3016
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590000861"
variation 3018
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1257825267"
variation 3019
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1476929728"
variation 3020
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:773939741"
variation 3021
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1199749295"
variation 3024
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1268693928"
variation 3025
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:771918484"
variation 3026
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:772968534"
variation 3027
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:368791581"
variation 3028
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1454424276"
variation 3030
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133906812"
variation 3031
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1200638891"
variation 3033
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:766151814"
variation 3037
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:983229924"
variation 3038
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:776467523"
variation 3041
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:908616884"
variation 3042
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:759454826"
variation 3045
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:765317734"
variation 3046
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851283080"
variation 3047
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:941479176"
variation 3048
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:752836080"
variation 3049
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1318914837"
variation 3050
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1590001080"
variation 3057
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:764345648"
variation 3058
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851284021"
variation 3060
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1387547863"
variation 3063
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1303695342"
variation 3064
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:556496771"
variation 3065
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:757591403"
variation 3070
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:574711696"
variation 3071
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1331107517"
variation 3072
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851285121"
variation 3073
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1590001162"
variation 3074
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:781551217"
variation 3075
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1220506232"
variation 3076
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1590001187"
variation 3077
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1407498903"
variation 3081
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:746374262"
variation 3087
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851286122"
variation 3089
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:756701345"
variation 3090
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1211209380"
variation 3092
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851286938"
variation 3098
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:780702310"
variation 3099
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851287302"
variation 3104
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:747701115"
variation 3105
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:771687718"
variation 3108
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1413580384"
variation 3109
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:962140588"
variation 3110
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:976145243"
variation 3116
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:777592361"
variation 3117
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1157657574"
variation 3121
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1402208941"
variation 3123
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851288279"
variation 3124
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1411611036"
variation 3125
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1460684927"
variation 3127
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851288704"
variation 3128
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851288842"
variation 3131
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:921452117"
variation 3132
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851289124"
variation 3133
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1590001329"
variation 3138
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:376187099"
variation 3140
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1295465666"
variation 3144
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:776432076"
variation 3145
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1386472605"
variation 3147
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:141726768"
variation 3148
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:769758760"
variation 3151
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:554126222"
variation 3153
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851290572"
variation 3156
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851290768"
variation 3160
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:199549347"
variation 3161
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:764116745"
variation 3165
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:986379770"
variation 3169
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1246763144"
variation 3171
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1227060568"
variation 3174
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851291821"
variation 3175
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1177109703"
variation 3176
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1263267741"
variation 3182
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851292306"
variation 3183
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:751732798"
variation 3184
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1287154805"
variation 3185
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:150436471"
variation 3186
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:750866450"
variation 3187
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851292761"
variation 3192
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:756516259"
variation 3193
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:375024485"
variation 3195
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851293256"
variation 3196
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1250475715"
variation 3198
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1424709004"
variation 3199
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:754349112"
variation 3201
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851293867"
variation 3202
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1367130443"
variation 3203
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1424259786"
variation 3204
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:369095063"
variation 3205
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1372422706"
variation 3206
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1222819487"
variation 3208
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1590001608"
variation 3210
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:138231164"
variation 3212
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1052793166"
variation 3213
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1307300351"
variation 3214..3221
/gene="SEMA4G"
/replace="tctg"
/replace="tctgtctg"
/db_xref="dbSNP:1851296377"
variation 3216
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:149579572"
variation 3216
/gene="SEMA4G"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1056241246"
variation 3221
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851297087"
variation 3223
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1012519597"
variation 3224
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851297556"
variation 3226
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851297775"
variation 3227
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:770679319"
variation 3231
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851298209"
variation 3232..3233
/gene="SEMA4G"
/replace=""
/replace="g"
/db_xref="dbSNP:1851298451"
variation 3238
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:780708778"
variation 3239
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1011343221"
variation 3243
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:745721149"
variation 3244
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1276335802"
variation 3247
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:769527048"
variation 3248
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851299997"
variation 3252
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:879129411"
variation 3254
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1373716210"
variation 3255
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:775434918"
variation 3256
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:762807711"
variation 3262
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1483848011"
variation 3265
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:768734270"
variation 3272
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851301714"
variation 3275
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1173041083"
variation 3278
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:969880106"
variation 3279
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1003167771"
variation 3288
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1180250824"
variation 3290
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1257290025"
variation 3299
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851302969"
variation 3302..3304
/gene="SEMA4G"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1183256014"
variation 3304
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1482030451"
variation 3306..3308
/gene="SEMA4G"
/replace="ccc"
/replace="ccccc"
/db_xref="dbSNP:1256227888"
variation 3306
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133908720"
variation 3307
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1023540260"
variation 3314
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851304104"
variation 3317
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1436403588"
variation 3318
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:887726997"
variation 3320
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133908809"
variation 3321
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851304584"
variation 3322
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:781204292"
variation 3325
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851305040"
variation 3327
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1014839064"
variation 3330
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851305511"
variation 3331
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:962032640"
variation 3345
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:976114197"
variation 3347
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:745690393"
variation 3350
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851306652"
variation 3351
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851306867"
variation 3352
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851307077"
variation 3361
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851307315"
variation 3366
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:950718210"
variation 3368..3369
/gene="SEMA4G"
/replace=""
/replace="ag"
/db_xref="dbSNP:1590001957"
variation 3371..3396
/gene="SEMA4G"
/replace=""
/replace="caggcccagccaaagccccctcctca"
/db_xref="dbSNP:1590001967"
variation 3373
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851308106"
variation 3374
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851308337"
variation 3375
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:953557741"
variation 3376
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1362537886"
variation 3380
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:986736713"
variation 3384
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:982791219"
variation 3386..3390
/gene="SEMA4G"
/replace="ccccc"
/replace="cccccc"
/db_xref="dbSNP:1851309403"
variation 3387
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1410299026"
variation 3392
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:908564430"
variation 3395..3396
/gene="SEMA4G"
/replace=""
/replace="ca"
/db_xref="dbSNP:2133909252"
variation 3398
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:962745699"
variation 3399
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1453609825"
variation 3401
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:974131731"
variation 3402
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:921398275"
variation 3403
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851310611"
variation 3404
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1308719600"
variation 3408
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133909360"
variation 3411
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1564800882"
variation 3415
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851311037"
variation 3417
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1416775905"
variation 3419
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851311226"
variation 3420
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1193893340"
variation 3422
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:932827701"
variation 3425
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1385143611"
variation 3427
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:947584470"
variation 3429
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:977712151"
variation 3431
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1242406016"
variation 3432
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851312352"
variation 3433
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1333845024"
variation 3434
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:564705467"
variation 3435
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:912794871"
variation 3436
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1342470994"
variation 3438
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1331866472"
variation 3443
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851313372"
exon 3449..4575
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 3449
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1169802472"
variation 3452
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133910482"
variation 3454
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1358850075"
variation 3458
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:761133475"
variation 3459
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1191685942"
variation 3460
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851322719"
variation 3462
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:565832622"
variation 3463
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1301023166"
variation 3465
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1238599331"
variation 3466
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:140873008"
variation 3467..3470
/gene="SEMA4G"
/replace="atat"
/replace="atatat"
/db_xref="dbSNP:1180219371"
variation 3468
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:775161961"
variation 3469
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851323614"
variation 3471
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1435583593"
variation 3472
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1347264509"
variation 3478
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:755490675"
variation 3479
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1022174562"
variation 3480
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851324366"
variation 3482
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1282490941"
variation 3491
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1232746478"
variation 3493
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851325083"
variation 3499..3501
/gene="SEMA4G"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1564801111"
variation 3499
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1015510000"
variation 3502
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:551143626"
variation 3504
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1309192746"
variation 3505
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1446522565"
variation 3506
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851326399"
variation 3508
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1313501848"
variation 3510
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851326936"
variation 3511
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851327156"
variation 3513
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1381487456"
variation 3519
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1370845164"
variation 3528
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1212785459"
variation 3529
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:962694375"
variation 3530
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851328377"
variation 3533
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:11591349"
variation 3534
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:536866327"
variation 3535
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1250348904"
variation 3539
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1447859281"
variation 3540
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1186203566"
variation 3541
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:977649336"
variation 3544
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133911153"
variation 3548
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:756712868"
variation 3551
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1204147027"
variation 3552
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:556345883"
variation 3553
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1434047317"
variation 3555
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851330601"
variation 3557
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1173815254"
variation 3558
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:567995095"
variation 3559
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:986972740"
variation 3562
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1322261528"
variation 3568
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1386272160"
variation 3569
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1468467340"
variation 3570
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851331669"
variation 3571
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:745459702"
variation 3573
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:755937099"
variation 3574
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851332127"
variation 3577
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242453332"
variation 3578
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:11190780"
variation 3579
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1369013608"
variation 3583
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1217004954"
variation 3585
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:749061715"
variation 3593
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1323427412"
variation 3594
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:768679541"
variation 3595
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:562213978"
variation 3598
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1463832678"
variation 3599
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1215245125"
variation 3601
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1392099800"
variation 3604
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1247539943"
variation 3605
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851334603"
variation 3607
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1489476783"
variation 3608
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851335052"
variation 3613
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:774150942"
variation 3614
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1330576370"
variation 3615
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:554180516"
variation 3616
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1161357971"
variation 3617
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1222920929"
variation 3622..3626
/gene="SEMA4G"
/replace="ct"
/replace="cttct"
/db_xref="dbSNP:1409419478"
variation 3625..3629
/gene="SEMA4G"
/replace="ct"
/replace="ctcct"
/db_xref="dbSNP:1399901647"
variation 3630
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851337089"
variation 3631
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1164988814"
variation 3633
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1347204536"
variation 3636..3640
/gene="SEMA4G"
/replace="tt"
/replace="ttctt"
/db_xref="dbSNP:1851337943"
variation 3638
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1351283007"
variation 3640
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851338509"
variation 3646
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:748317224"
variation 3649
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1301958846"
variation 3653
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851339309"
variation 3658
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1350650732"
variation 3659
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:771987099"
variation 3660
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:909015462"
variation 3661
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:947024954"
variation 3663
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1348931588"
variation 3679
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1044109678"
variation 3680
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851341027"
variation 3688
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851341287"
variation 3692
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851341554"
variation 3694
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1223598937"
variation 3697
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:941896553"
variation 3703
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1590003340"
variation 3704..3707
/gene="SEMA4G"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:749161619"
variation 3704
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:867056759"
variation 3706
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851342959"
variation 3707
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1341846221"
variation 3711
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1323698735"
variation 3714
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1219725456"
variation 3715
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:897779980"
variation 3716
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1483432059"
variation 3718
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:766759551"
variation 3719
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133912160"
variation 3721
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1398820091"
variation 3724
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:938445182"
variation 3725
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1249568875"
variation 3727..3729
/gene="SEMA4G"
/replace="t"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:1564801421"
variation 3735
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851345504"
variation 3737
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851345730"
variation 3739
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133912278"
variation 3741..3743
/gene="SEMA4G"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:34661749"
variation 3741
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1469396700"
variation 3743
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1590003500"
variation 3746
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1051674712"
variation 3747
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1473643656"
variation 3748
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415748001"
variation 3754
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1403242646"
variation 3756
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851347694"
variation 3757
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851347910"
variation 3758
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413115744"
variation 3762
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1186071819"
variation 3763
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1162547813"
variation 3764
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1370560535"
variation 3770
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:889128459"
variation 3771
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851348837"
variation 3772
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1431132181"
variation 3777..3785
/gene="SEMA4G"
/replace="ctcc"
/replace="ctcccctcc"
/db_xref="dbSNP:1310336433"
variation 3779
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851349496"
variation 3780
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1056944101"
variation 3783
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851350086"
variation 3785
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:886274992"
variation 3787
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1828080527"
variation 3790..3796
/gene="SEMA4G"
/replace="cct"
/replace="ccttcct"
/db_xref="dbSNP:1442168150"
variation 3790
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1285150909"
variation 3791
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:150176473"
variation 3794
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1284040676"
variation 3799
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1243979563"
variation 3801
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1454985511"
variation 3805
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1016127185"
variation 3806
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1342914307"
variation 3807
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1207413139"
variation 3810
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1272637340"
variation 3812..3817
/gene="SEMA4G"
/replace=""
/replace="atcagc"
/db_xref="dbSNP:1437134295"
variation 3812
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:546548368"
variation 3815..3824
/gene="SEMA4G"
/replace=""
/replace="agcctcccca"
/db_xref="dbSNP:1232285107"
variation 3818
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851353656"
variation 3819
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851353903"
variation 3820..3823
/gene="SEMA4G"
/replace="ccc"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1851354331"
variation 3820
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:999055334"
variation 3821..3825
/gene="SEMA4G"
/replace="c"
/replace="cccac"
/db_xref="dbSNP:1188248769"
variation 3822
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:558511473"
variation 3824
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851355064"
variation 3825
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1471688492"
variation 3826..3827
/gene="SEMA4G"
/replace=""
/replace="gtgtga"
/db_xref="dbSNP:1279740182"
variation 3826
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564801584"
variation 3827
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1182551535"
variation 3833
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1390425592"
variation 3834
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:866465441"
variation 3836
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:899127927"
variation 3837
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851356441"
variation 3843..3844
/gene="SEMA4G"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1851356699"
variation 3848..3850
/gene="SEMA4G"
/replace="t"
/replace="tat"
/db_xref="dbSNP:776469814"
variation 3848
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:1564801613"
variation 3849
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:995448141"
variation 3850
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1406943937"
variation 3851..3856
/gene="SEMA4G"
/replace="gaga"
/replace="gagaga"
/db_xref="dbSNP:1031921038"
variation 3852
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1352660512"
variation 3853
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1166136937"
variation 3855
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:960318556"
variation 3859
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851358185"
variation 3864
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1217254719"
variation 3867
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:993082702"
variation 3868
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851358464"
variation 3869
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851358683"
variation 3871
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:576676078"
variation 3872
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851359112"
variation 3874
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:954125817"
variation 3875
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1409881469"
variation 3880
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1590004029"
variation 3881
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1335465291"
variation 3882
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1361197103"
variation 3884
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1450956457"
variation 3890
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1314573273"
variation 3891
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242083934"
variation 3893..3894
/gene="SEMA4G"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1366179476"
variation 3893
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851361189"
variation 3895
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1734059355"
variation 3896..3899
/gene="SEMA4G"
/replace="aaca"
/replace="aacaaca"
/db_xref="dbSNP:398114688"
variation 3897..3904
/gene="SEMA4G"
/replace="acac"
/replace="acacacac"
/db_xref="dbSNP:146737296"
variation 3897
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851362081"
variation 3899
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1470152414"
variation 3900
/gene="SEMA4G"
/replace=""
/replace="c"
/db_xref="dbSNP:1554885387"
variation 3902..3905
/gene="SEMA4G"
/replace="c"
/replace="cacc"
/db_xref="dbSNP:1564801730"
variation 3902
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:980911684"
variation 3910
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:908989869"
variation 3911
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1318120156"
variation 3914
/gene="SEMA4G"
/replace=""
/replace="a"
/db_xref="dbSNP:1851363694"
variation 3915
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1297128475"
variation 3916..3917
/gene="SEMA4G"
/replace=""
/replace="at"
/db_xref="dbSNP:201653131"
variation 3917
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851363979"
variation 3918
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:941859324"
variation 3920
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1275426272"
variation 3926
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:544003449"
variation 3933
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:561580399"
variation 3938
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:987306998"
variation 3939
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1761267634"
variation 3945
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851365080"
variation 3946
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:760046546"
variation 3949
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851365638"
variation 3957
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:570837619"
variation 3959
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851366097"
variation 3960
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1461145737"
variation 3961
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:956410819"
variation 3965
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1172757131"
variation 3966
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590004294"
variation 3970
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:765696472"
variation 3971..3978
/gene="SEMA4G"
/replace="ctgt"
/replace="ctgtctgt"
/db_xref="dbSNP:1851367609"
variation 3971
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851367435"
variation 3973
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:776736066"
variation 3985
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:541757083"
variation 3986
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1455911411"
variation 3988
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133914046"
variation 3990
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:947649741"
variation 3991
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:540658889"
variation 3996
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1458477096"
variation 3998
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851368804"
variation 4013
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:979738620"
variation 4014
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133914138"
variation 4015
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1419920691"
variation 4033
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851369510"
variation 4036
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:926970920"
variation 4038
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:938406307"
variation 4045
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1345587818"
variation 4050..4058
/gene="SEMA4G"
/replace="ggatg"
/replace="ggatggatg"
/db_xref="dbSNP:1156991738"
variation 4051
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1590004435"
variation 4056
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1411538590"
variation 4057
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1447292211"
variation 4058
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1057292576"
variation 4068
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1401448436"
variation 4069
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:148889377"
variation 4071
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1354019972"
variation 4074
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1357855929"
variation 4075
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:185501392"
variation 4076
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1437149072"
variation 4077
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1393859490"
variation 4080
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1314077837"
variation 4084..4085
/gene="SEMA4G"
/replace="c"
/replace="cc"
/db_xref="dbSNP:745620184"
variation 4090
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851373532"
variation 4091
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1357883329"
variation 4093
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1058101"
variation 4094..4098
/gene="SEMA4G"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1564801889"
variation 4095
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1043523463"
variation 4097
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1440759734"
variation 4098
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1037520890"
variation 4099
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851374834"
variation 4105
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851375125"
variation 4109
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851375359"
variation 4114..4118
/gene="SEMA4G"
/replace="tc"
/replace="tcctc"
/db_xref="dbSNP:1851375586"
variation 4115
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1287105200"
variation 4116
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:899075093"
variation 4118
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851376270"
variation 4119
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:758453345"
variation 4120
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:999022475"
variation 4122
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:533032857"
variation 4124
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851377123"
variation 4129
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851377286"
variation 4131..4139
/gene="SEMA4G"
/replace="gggaaaggg"
/replace="gggaaagggggaaaggg"
/db_xref="dbSNP:1237569905"
variation 4131
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1276666015"
variation 4137
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851377980"
variation 4138..4144
/gene="SEMA4G"
/replace="ggag"
/replace="ggaggag"
/db_xref="dbSNP:1212458091"
variation 4144
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:539958411"
variation 4150
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1031806643"
variation 4152
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:996061169"
variation 4153..4157
/gene="SEMA4G"
/replace="tgtct"
/replace="tgtctgtct"
/db_xref="dbSNP:1851379088"
variation 4153..4155
/gene="SEMA4G"
/replace="t"
/replace="tgt"
/db_xref="dbSNP:1851378916"
variation 4154
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1276056518"
variation 4155
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1318520975"
variation 4158
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851379758"
variation 4161
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1028300853"
variation 4162
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1222315298"
variation 4167
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:145456828"
variation 4169
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851380461"
variation 4173
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1259577119"
variation 4174
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851380817"
variation 4175
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851380992"
variation 4181
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:969446661"
variation 4185
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851381422"
variation 4189
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1313689869"
variation 4190
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851381840"
variation 4193
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851382067"
variation 4199
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:980495734"
variation 4201
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1016423976"
variation 4203
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851382772"
variation 4207
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:764283941"
variation 4208
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851383229"
variation 4209
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851383454"
variation 4210
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:889784981"
variation 4211
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851383892"
variation 4216
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851384118"
variation 4217
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1482005638"
variation 4218
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1008277694"
variation 4219
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:751801892"
variation 4225
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133915301"
variation 4230
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1590004825"
variation 4233
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851385217"
variation 4234..4235
/gene="SEMA4G"
/replace=""
/replace="ct"
/db_xref="dbSNP:971792769"
variation 4234
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851385462"
variation 4235
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:919060865"
variation 4237
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851386135"
variation 4246
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851386346"
variation 4247
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1365943648"
variation 4248
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1160574437"
variation 4249
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:549901293"
variation 4250
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851387327"
variation 4251
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:987778470"
variation 4253
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:956145941"
variation 4257
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1189614913"
variation 4258
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1484440106"
variation 4262
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851388353"
variation 4263
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851388576"
variation 4264
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:722435"
variation 4266
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851389219"
variation 4267
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133915599"
variation 4269
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1174615834"
variation 4271
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1377821148"
variation 4272
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1486785377"
variation 4274
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851390176"
variation 4276
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851390425"
variation 4277
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1021817552"
variation 4281
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851390914"
variation 4285
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1258766345"
variation 4286
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:13114"
variation 4288
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:530575708"
variation 4295
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1322070191"
variation 4296
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851392002"
variation 4298
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851392246"
variation 4300
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590005004"
variation 4302
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851392702"
variation 4306
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1294208197"
variation 4309
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851393161"
variation 4314
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:796584525"
variation 4315
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851393640"
variation 4318
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1443718900"
variation 4319
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:549209014"
variation 4320..4324
/gene="SEMA4G"
/replace="ccccc"
/replace="cccccc"
/db_xref="dbSNP:1851394245"
variation 4322
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851394479"
variation 4324
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851394644"
variation 4325
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1272765213"
variation 4326
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:535391514"
variation 4329
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133915982"
variation 4333
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:722434"
variation 4334
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:756150215"
variation 4335
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851395747"
variation 4337..4345
/gene="SEMA4G"
/replace="tga"
/replace="tgaggatga"
/db_xref="dbSNP:1851395903"
variation 4340
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1287595742"
variation 4342
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1590005102"
variation 4343..4348
/gene="SEMA4G"
/replace="tg"
/replace="tgactg"
/db_xref="dbSNP:1282127784"
variation 4347..4349
/gene="SEMA4G"
/replace="t"
/replace="tgt"
/db_xref="dbSNP:1851396880"
variation 4348
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851397104"
variation 4351
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851397297"
variation 4352
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851397538"
variation 4357
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851397765"
variation 4361
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1453577215"
variation 4362
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851398062"
variation 4363
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1339982424"
variation 4368
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:992545494"
variation 4369
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1473984676"
variation 4373
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:377579383"
variation 4376
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1193217573"
variation 4380
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1429752865"
variation 4381
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:535979784"
variation 4383
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851399630"
variation 4384
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1053207362"
variation 4391
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1204475752"
variation 4396
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1468760178"
variation 4399
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851400265"
variation 4400
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:895968520"
variation 4407
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:547453410"
variation 4408
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1215821939"
variation 4411
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1014460178"
variation 4413
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851401422"
variation 4416
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1272754894"
variation 4420
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590005244"
variation 4423
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:566052365"
variation 4424
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1228291159"
variation 4425
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:539856889"
variation 4426..4433
/gene="SEMA4G"
/replace="aatg"
/replace="aatgaatg"
/db_xref="dbSNP:1851402794"
variation 4429
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1294126122"
variation 4432
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:1245235656"
variation 4433
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1023629686"
variation 4442
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:907599520"
variation 4443
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851403820"
variation 4444
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1194666457"
variation 4446
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1459569804"
variation 4449
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851404319"
variation 4452
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1397200065"
variation 4455
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1006217092"
variation 4457
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851405001"
variation 4461
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:940472396"
variation 4465
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1370830712"
variation 4466
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851405676"
variation 4469
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851405873"
variation 4471
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851406098"
variation 4474
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564802346"
variation 4477
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1168572915"
variation 4481
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1454629864"
variation 4485
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851406807"
variation 4491
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1015896546"
variation 4492
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1183846917"
variation 4493
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1590005486"
variation 4494..4495
/gene="SEMA4G"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1851407769"
variation 4494
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1037468969"
variation 4495
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1267016453"
variation 4496
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851408064"
variation 4498
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:971763006"
variation 4499
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:780109310"
variation 4509
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851408894"
variation 4512
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:920446283"
variation 4514
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1590005630"
variation 4515..4520
/gene="SEMA4G"
/replace="ggggag"
/replace="ggggagggggag"
/db_xref="dbSNP:1851409933"
variation 4515
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1026045787"
variation 4516
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1249625499"
variation 4520
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1397803701"
variation 4521
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851410880"
variation 4523
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:11190781"
variation 4524
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851411332"
variation 4526
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:375892284"
variation 4533
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590005760"
variation 4535
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851412105"
variation 4536
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:1348958879"
variation 4536
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590005788"
variation 4539
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1441105677"
variation 4540
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:890411724"
variation 4541
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133917246"
variation 4542
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1008640180"
variation 4543
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:576811967"
variation 4544..4545
/gene="SEMA4G"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1851413621"
variation 4545
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:537243928"
variation 4546
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:555966416"
variation 4547
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:573637014"
variation 4549
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:934667679"
variation 4550
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1171676783"
regulatory 4553..4558
/regulatory_class="polyA_signal_sequence"
/gene="SEMA4G"
/note="hexamer: AATAAA"
variation 4561
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:866768376"
variation 4562
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1010346124"
variation 4563
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851414998"
variation 4564
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851415299"
variation 4568
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:917372450"
variation 4569..4572
/gene="SEMA4G"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1439739794"
variation 4570
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590006249"
variation 4572
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851416502"
polyA_site 4575
/gene="SEMA4G"
/note="major polyA site"
ORIGIN
agccgcggccccttcctctcgcagctggtgctgtggggccgcggagccgcgcgtcgctgtctctatggccccggatccgagcgcaaagctgggccaggcctttctcaccaccaagtcccccggtcctgcatgacggctctagaggggcgcgggccaggcctcgggctgcgcggggtgcaaaccggccaccacggagtcggggaccagcgcggggagggggccgcgtggcgaacagtgttccccaggatctgggtcacgtctcccggcgtccggcgggatcgaaggagagcttgtcctcgagctgcagcagtagagactgagaaaacggacctcagaaaaccaggactagctctactgtcgggggcagggtgaccccatcagtaacctacaacccctctagaacttcacaactccctctcaccatggagtttgcatttgatgcagaaaggcatgtgatccctccctccttctgacctcttagctggggattccatggccacacaaccctgtgactccatgtccccccgattccaggaccccccatggccccatgattccttgactcctatgaccttatgacccctgaccttccaagtgacttccttggactttgacccctgtgactgtgcttcccattccccgcccccacaacctgtgactctggctccctttgggggtcttgttagtctgggcctccccaggaagatgtgggggaggctctggcccctcctcctcagcatcctcacagcaactgcagtcccaggaccctcactgcggagaccgtctagagaactagatgccacccctcggatgaccataccctatgaagagctctctgggacccggcacttcaagggccaagcccagaactactcaacactgctgctggaggaggcctcagcaaggctgctggtgggagcccgaggtgccctgttctctctcagtgccaacgacataggagatggggctcacaaagagatccactgggaagcctccccagagatgcaaagcaaatgtcatcaaaaagggaaaaacaaccagacggagtgctttaaccatgtgcggttcctgcagcggctcaattctacccacctctatgcatgtgggactcacgccttccagcccctctgtgcagccattgatgctgaggccttcaccttgccaaccagcttcgaggaggggaaggagaagtgtccttatgacccagcccgtggcttcacaggcctcatcattgatggaggcctctacacagccactaggtatgaattccggagcattcctgacatccgccggagccgccacccacactccctgagaactgaggagacaccaatgcattggctcaatgatgcggagtttgtgttctccgtcctcgtgcgggagagcaaggccagtgcagtgggtgatgatgacaaggtgtactacttcttcacggagcgtgccactgaggagggctctggcagcttcactcagagccgcagcagtcaccgtgtggcccgtgtggctcgtgtctgcaagggagacctgggagggaagaagatcctgcagaagaagtggacttccttcctgaaagcccgtctcatctgccacattccactgtatgagacactgcgtggggtctgcagcctggatgctgaaacctcaagccgtacacacttctatgcagccttcacgctgagcacacagtggaagaccctggaggcctcagccatctgccgctatgacctggcagagatccaggctgtctttgcaggaccctatatggaataccaggatggttcccggcgctggggtcgctatgagggtggggtgcctgagccccggcctggctcgtgtatcacagattcattgcgcagccaaggctacaattcatcccaagacttgccatccctggtcctggactttgtaaagttgcacccactgatggctcggcccgttgtgcccacacgtggacggcccctgctgctcaagcgcaacatacgctacacacaccttacagggacacctgtcaccacgcctgctggacctacctatgacctgctctttctgggcacagctgatggctggatccacaaggccgtagtcctgggctctgggatgcacattattgaagagacacaagtgttcagggagtcccagtctgtggaaaatctagtcatctctctattgcagcacagcctctatgtgggggctcctagcggagtcatccagctaccactctccagctgctcccgctaccgatcctgctatgactgcatcttggcccgagacccctactgtggctgggaccctggcacccatgcctgcgcagcagccaccaccatagccaacaggacagcactgatacaggacatagagagaggaaatcgaggctgtgagagcagcagggatacagggccaccaccaccactgaagacccgctctgtgctccggggtgatgatgtcctcctgccctgtgaccagccatccaacctggcccgggccttgtggctactcaatgggagcatgggcctgagcgatgggcagggtggctaccgtgtgggcgtggacgggctgctggttacagatgcacagcctgagcacagtggcaactatggctgctatgccgaggaaaatggcctccgcaccctgctggcctcctatagtctcacagtccggccagccactcctgccccagctccaaaagcccctgccacacctggggcacagctggcacctgatgtgagactgctctatgtgctagccattgccgcgcttggtggcctctgcctcatcctggcctcctccctcctctatgtggcctgtctgcgggaaggcagacgagggcgccgacggaaatactcactgggtcgggccagccgggcaggaggatctgcggtgcaactgcagacagtctcaggccagtgtcctggagaggaagatgagggtgatgatgagggggctgggggcctggagggcagctgtctccagatcatccctggggagggagccccagccccaccacccccaccgcccccaccgccaccggctgagctgaccaatggcttggtggcactgcccagccggctgcggaggatgaatggcaatagctatgtgcttctgaggcagagcaacaatggagtaccagcagggccctgctccttcgccgaggaactcagccgcatcctggaaaaaaggaagcacacgcagctcgtggagcagctagatgagagctctgtctgagcccagcctcccagaacaaatgctcttccaagccagcctatctgtcccaggctgggccactgcctccctaacacagccaccctcccttcattacccccactccatacccttctcccaactttttgatgtccctgtagggctggccagtcaggcccagccaaagccccctcctcagtctccacagacccacatgtgagcagcccaggcccatcggtgctcctcagaggcagggctctgcaggtccatatgggctcaatgtcaccaccctctgcatggccctgtgtgctggatggtcctgaaaccagacaagacctctgccagccacctaagccctgcgtacattcacatgcacacatggaagaatgtttatcggctgggctgcagtgcccccaccctcaccttctcctggtgcattcttgtttcatccctgcttctggacttggggtaccctcccaattgccacatcctatctggtcctcttccccagccccatgtggtgacctctttgtcaagagcttgggaacgggccagcctggggaggtaagactgcatcactcccctcctctcccttcctgtgtggcccttgtgaatcagcctccccactctccttggtcattctcaagagtatgagagacagagctccaggcatgtcccatccccatgcacatgtggtaacacacacctgtatcacacatgtgcttacatttccactcacatgcacctctgagcctcccttgctgtcttggacctgtctgttgggtttagtccgtggacatttcagagggagatccccctcccatttaactgtcctcacaggcccttgcctaggatggatgaccaacactgcactcaatgagccagcctctcttttgggggaatcaagcatttgcttcctctagactacagcagggaaagggaggagaaatctgatgtctcaactggcacatgaagcccattcttggaactatgcaaagggcagaggctgggagtttggacgcttagctcctacccctgtcctacctcaccggggcactttcaggggccaggggcctctgaagtctctaggcctatatgggacaatcaattctgactgagctcccccattcccctcgggtgaggatgactgttatttttgtagctgagaacgtggaatcccacgggtttttactgcccttcacccaacctctcccacctccaccccacaatgaatgtatttattgtgagaatggctacacttctttaggaatgcccccacttacaaccaggtgggtggaacaggcatgtgacagagtggggagcctgggctcagctcctccccctgccgttggttaataaacaccctttttccccaca
//
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.
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