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Previous release (v1)
2024-04-27 10:16:38, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_001203244 3230 bp mRNA linear PRI 26-JUN-2023
DEFINITION Homo sapiens semaphorin 4G (SEMA4G), transcript variant 2, mRNA.
ACCESSION NM_001203244
VERSION NM_001203244.1
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 3230)
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 3230)
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 3230)
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 3230)
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 3230)
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 3230)
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 3230)
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 3230)
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 BC051030.1, BC128579.1 and
BC020960.1.
Summary: Semaphorins are a large family of conserved secreted and
membrane associated proteins which possess a semaphorin (Sema)
domain and a PSI domain (found in plexins, semaphorins and
integrins) in the N-terminal extracellular portion. Based on
sequence and structural similarities, semaphorins are put into
eight classes: invertebrates contain classes 1 and 2, viruses have
class V, and vertebrates contain classes 3-7. Semaphorins serve as
axon guidance ligands via multimeric receptor complexes, some (if
not all) containing plexin proteins. Multiple transcript variants
encoding different isoforms have been found for this gene.
[provided by RefSeq, Feb 2011].
##Evidence-Data-START##
Transcript exon combination :: BC128579.1 [ECO:0000332]
RNAseq introns :: partial sample support SAMEA1968540,
SAMEA1968832 [ECO:0000350]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-183 BC051030.1 403-585
184-2858 BC128579.1 1-2675
2859-3230 BC020960.1 817-1188
FEATURES Location/Qualifiers
source 1..3230
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="10"
/map="10q24.31"
gene 1..3230
/gene="SEMA4G"
/note="semaphorin 4G"
/db_xref="GeneID:57715"
/db_xref="HGNC:HGNC:10735"
/db_xref="MIM:618991"
exon 1..508
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 5
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1030762196"
variation 6
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850663596"
variation 10
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850663843"
variation 12
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850663913"
variation 13
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:557949623"
variation 25
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1335694004"
variation 28
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1457386306"
variation 29
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850664129"
variation 36
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1365050521"
variation 37
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850664254"
variation 38
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:892265119"
variation 39
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:570166640"
variation 40
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1414497874"
variation 41
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:867026643"
variation 42
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1394108765"
variation 43
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850664603"
variation 44
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:943019392"
variation 45
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:761543704"
variation 49
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1589978234"
variation 54
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:537435528"
variation 60
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:60278872"
variation 62
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:111933864"
variation 64
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1262698358"
variation 65
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850665019"
variation 66
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850665075"
variation 71
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1850665124"
variation 78
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1213813489"
variation 83
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850665221"
variation 90
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1316377096"
variation 93
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:980739677"
variation 97
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:182450988"
variation 98
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850665375"
variation 99
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850665422"
variation 100
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1589978258"
variation 102
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1034747287"
variation 104
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1449004233"
variation 107
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1589978265"
variation 112
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850665683"
variation 115
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1381078635"
variation 119
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850665781"
variation 121
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:934446804"
variation 123
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:960088474"
variation 128
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850665939"
variation 130..131
/gene="SEMA4G"
/replace=""
/replace="gtg"
/db_xref="dbSNP:1850666070"
variation 130
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:115583289"
variation 131
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850666120"
variation 132
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1386772616"
variation 135
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1850666516"
variation 146..150
/gene="SEMA4G"
/replace="ct"
/replace="cttct"
/db_xref="dbSNP:1330691442"
variation 154
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850666602"
variation 158
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850666651"
variation 163..166
/gene="SEMA4G"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:771249674"
variation 166
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1286727183"
variation 169
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1234279287"
variation 171
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850666856"
variation 173
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850666906"
variation 179
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:747642385"
variation 181
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1850667028"
variation 184..186
/gene="SEMA4G"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1365607676"
variation 193
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1850667141"
variation 194
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:553501059"
variation 197
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850667233"
variation 200..205
/gene="SEMA4G"
/replace="ccccc"
/replace="cccccc"
/replace="ccccccc"
/db_xref="dbSNP:1276939230"
variation 200
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850667277"
variation 201
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:578092859"
variation 205
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:949932767"
variation 206
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1044290858"
variation 210
/gene="SEMA4G"
/replace="c"
/replace="ctgc"
/db_xref="dbSNP:1850667555"
variation 216..221
/gene="SEMA4G"
/replace="cccccc"
/replace="ccccccc"
/db_xref="dbSNP:1198554590"
variation 216
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1259348483"
variation 217
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1485595178"
variation 219
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:186703368"
variation 222
/gene="SEMA4G"
/replace=""
/replace="a"
/db_xref="dbSNP:1850667867"
variation 222
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:973566758"
variation 223
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1207497990"
variation 225
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1358003866"
variation 230
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850668057"
variation 231
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1807570131"
variation 231
/gene="SEMA4G"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1807570306"
variation 237
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850668128"
variation 238
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850668209"
variation 241
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850668271"
variation 244
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1266084809"
variation 250
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1451781054"
variation 255
/gene="SEMA4G"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1328543428"
variation 255
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1293029193"
misc_feature 256..258
/gene="SEMA4G"
/note="upstream in-frame stop codon"
variation 257
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1381265281"
variation 259
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1345600213"
variation 261
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850668683"
variation 262
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850668734"
variation 263
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1304369840"
variation 266
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:905793660"
variation 267
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850668844"
variation 276
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:560469443"
variation 281
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850668946"
variation 282
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:563225955"
variation 285
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850669047"
variation 291
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850669092"
variation 293
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1364956082"
variation 296
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1168394557"
variation 298
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:1850669406"
variation 298
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:771649939"
variation 303
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1371109660"
variation 305
/gene="SEMA4G"
/replace=""
/replace="g"
/db_xref="dbSNP:1850669696"
variation 307
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1191340004"
variation 308
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1050718409"
variation 313
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1477407403"
variation 317
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:890089013"
variation 318
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850670117"
variation 320
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1016975985"
variation 321
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1442004696"
variation 322
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1269856612"
variation 323
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850670356"
variation 326
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:897234872"
variation 328
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:944394849"
variation 329
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1268862242"
variation 330
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1052574006"
variation 338
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:192621867"
variation 340
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:752393071"
variation 342
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1564791838"
variation 343
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850671019"
variation 345
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850671101"
variation 346..348
/gene="SEMA4G"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1850671316"
variation 346
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1224898784"
variation 348
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:867629405"
variation 350
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1250557337"
variation 352..356
/gene="SEMA4G"
/replace="ggggg"
/replace="gggggg"
/db_xref="dbSNP:1345238361"
variation 352
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:758309995"
variation 353
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:777690359"
variation 355..357
/gene="SEMA4G"
/replace="ggt"
/replace="ggtggt"
/db_xref="dbSNP:1850671886"
variation 356
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:746967585"
variation 358
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:770865272"
variation 359..360
/gene="SEMA4G"
/replace=""
/replace="tt"
/db_xref="dbSNP:1850672187"
variation 359
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:781140045"
variation 366
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1010644581"
variation 372
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1430821467"
variation 376
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850672377"
variation 381
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1402602510"
CDS 385..2493
/gene="SEMA4G"
/note="isoform 2 precursor is encoded by transcript
variant 2; sema domain, immunoglobulin domain (Ig),
transmembrane domain (TM) and short cytoplasmic domain,
(semaphorin) 4G"
/codon_start=1
/product="semaphorin-4G isoform 2 precursor"
/protein_id="NP_001190173.1"
/db_xref="CCDS:CCDS55724.1"
/db_xref="GeneID:57715"
/db_xref="HGNC:HGNC:10735"
/db_xref="MIM:618991"
/translation="
MWGRLWPLLLSILTATAVPGPSLRRPSRELDATPRMTIPYEELSGTRHFKGQAQNYSTLLLEEASARLLVGARGALFSLSANDIGDGAHKEIHWEASPEMQSKCHQKGKNNQTECFNHVRFLQRLNSTHLYACGTHAFQPLCAAIDAEAFTLPTSFEEGKEKCPYDPARGFTGLIIDGGLYTATRYEFRSIPDIRRSRHPHSLRTEETPMHWLNDAEFVFSVLVRESKASAVGDDDKVYYFFTERATEEGSGSFTQSRSSHRVARVARVCKGDLGGKKILQKKWTSFLKARLICHIPLYETLRGVCSLDAETSSRTHFYAAFTLSTQWKTLEASAICRYDLAEIQAVFAGPYMEYQDGSRRWGRYEGGVPEPRPGSCITDSLRSQGYNSSQDLPSLVLDFVKLHPLMARPVVPTRGRPLLLKRNIRYTHLTGTPVTTPAGPTYDLLFLGTADGWIHKAVVLGSGMHIIEETQVFRESQSVENLVISLLQHSLYVGAPSGVIQLPLSSCSRYRSCYDCILARDPYCGWDPGTHACAAATTIANRSQGSRTALIQDIERGNRGCESSRDTGRALQVHMGSMSPPSAWPCVLDGPETRQDLCQPPKPCVHSHAHMEECLSAGLQCPHPHLLLVHSCFIPASGLGVPSQLPHPIWSSSPAPCGDLFVKSLGTGQPGEVRLHHSPPLPSCVALVNQPPHSPWSFSRV"
sig_peptide 385..435
/gene="SEMA4G"
/inference="COORDINATES: ab initio prediction:SignalP:4.0"
misc_feature 523..1902
/gene="SEMA4G"
/note="The Sema domain, a protein interacting module, of
semaphorins and plexins; Region: Sema; cl15693"
/db_xref="CDD:449580"
misc_feature 547..549
/gene="SEMA4G"
/note="N-linked (GlcNAc...) asparagine.
/evidence=ECO:0000255; propagated from
UniProtKB/Swiss-Prot (Q9NTN9.1); glycosylation site"
misc_feature 715..717
/gene="SEMA4G"
/note="N-linked (GlcNAc...) asparagine.
/evidence=ECO:0000255; propagated from
UniProtKB/Swiss-Prot (Q9NTN9.1); glycosylation site"
misc_feature 760..762
/gene="SEMA4G"
/note="N-linked (GlcNAc...) asparagine.
/evidence=ECO:0000255; propagated from
UniProtKB/Swiss-Prot (Q9NTN9.1); glycosylation site"
misc_feature 1546..1548
/gene="SEMA4G"
/note="N-linked (GlcNAc...) asparagine.
/evidence=ECO:0000255; propagated from
UniProtKB/Swiss-Prot (Q9NTN9.1); glycosylation site"
misc_feature 1903..>1986
/gene="SEMA4G"
/note="Plexin repeat; Region: PSI; pfam01437"
/db_xref="CDD:396154"
misc_feature 2008..2010
/gene="SEMA4G"
/note="N-linked (GlcNAc...) asparagine.
/evidence=ECO:0000255; propagated from
UniProtKB/Swiss-Prot (Q9NTN9.1); glycosylation site"
variation 385
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1191397762"
variation 387
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1344292943"
variation 388..411
/gene="SEMA4G"
/replace=""
/replace="tgggggaggctctggcccctcctc"
/db_xref="dbSNP:1564791884"
variation 389..393
/gene="SEMA4G"
/replace="ggggg"
/replace="gggggg"
/db_xref="dbSNP:1850672932"
variation 389
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:745907076"
variation 390
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:769754047"
variation 393
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850673074"
variation 399
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1393022504"
variation 402
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:775751808"
variation 404
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1043525758"
variation 405
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1167174298"
variation 414
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850673445"
variation 419
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:1850673633"
variation 419
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:763127413"
variation 423
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:141766082"
variation 424
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1850673834"
variation 425
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1469347701"
variation 427
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:201769907"
variation 428
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1363910803"
variation 430
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850674227"
variation 431
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:762257142"
variation 433
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850674430"
variation 434
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:768000743"
variation 435
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:753300939"
variation 436
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:765633702"
variation 438
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:528334576"
variation 446
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:764810125"
variation 447
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1322465491"
variation 449
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:752448070"
variation 452
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1261974981"
variation 454
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:150563616"
variation 455
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:751304450"
variation 456
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133857417"
variation 457
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850675630"
variation 460
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1195652118"
variation 461
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:139918504"
variation 462
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:571547734"
variation 463
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850676089"
variation 466
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850676178"
variation 469
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1202124518"
variation 471
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133857469"
variation 474
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:532192623"
variation 475
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:780081656"
variation 477
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:2133857483"
variation 479
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:867204232"
variation 480
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1159955320"
variation 487
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:749532175"
variation 488
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:768824226"
variation 491
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1850677171"
variation 493
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850677263"
variation 496
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:774700812"
variation 499
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:369789414"
variation 502
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:962113918"
variation 503..506
/gene="SEMA4G"
/replace="a"
/replace="atga"
/db_xref="dbSNP:1406530664"
variation 503
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:772310279"
variation 504
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1344402684"
variation 505
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378220105"
variation 506
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133857555"
exon 509..657
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 515
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:369353258"
variation 522
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:144341151"
variation 523
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:372839640"
variation 524
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1370809407"
variation 526
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:780136613"
variation 532
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:913597081"
variation 535
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:749297787"
variation 538
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1441420061"
variation 542
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:755205395"
variation 543
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850682502"
variation 546
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1360751746"
variation 552
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850682665"
variation 554
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1248834281"
variation 556
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850682797"
variation 557
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850682873"
variation 558
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1284517077"
variation 559
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:779253360"
variation 562
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:748287481"
variation 564
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1205748549"
variation 567..574
/gene="SEMA4G"
/replace="ggagg"
/replace="ggaggagg"
/db_xref="dbSNP:1850683258"
variation 568
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1234802535"
variation 571
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:199970914"
variation 573
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:756103359"
variation 578
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:747581175"
variation 582
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850683769"
variation 585
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1029721556"
variation 589
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1243856800"
variation 591
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1446315165"
variation 596
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:376810147"
variation 597
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1384733681"
variation 598
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1384572205"
variation 601
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:750643700"
variation 602
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:202147105"
variation 605
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1007038634"
variation 606
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1589978805"
variation 608
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1352343381"
variation 609
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1402573417"
variation 614..621
/gene="SEMA4G"
/replace="tctctc"
/replace="tctctctc"
/db_xref="dbSNP:1441071018"
variation 616
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850685194"
variation 617
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:199688982"
variation 619
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850685355"
variation 623
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:762606692"
variation 630
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:146573432"
variation 631
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:140040145"
variation 639
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1445693261"
variation 642
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850685679"
variation 644
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:761353685"
variation 645
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1387484882"
variation 646
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1056746530"
variation 650
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:373053309"
variation 653
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:750147136"
variation 655
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:760612775"
exon 658..720
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 663
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:765388169"
variation 664
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1385079315"
variation 670
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:200094625"
variation 672
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:879452513"
variation 673
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:752650927"
variation 674..677
/gene="SEMA4G"
/replace="c"
/replace="cccc"
/db_xref="dbSNP:1589979126"
variation 675
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:149776999"
variation 678
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:891205288"
variation 681
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1423146487"
variation 685
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850694572"
variation 691..693
/gene="SEMA4G"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1457139894"
variation 691
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1257694646"
variation 696
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:751823274"
variation 699
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1224318002"
variation 701..705
/gene="SEMA4G"
/replace="aaaaa"
/replace="aaaaaa"
/db_xref="dbSNP:769978574"
variation 701
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:757731950"
variation 702
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:368462093"
variation 709
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1221941297"
variation 714
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1274539366"
variation 716
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:746403415"
variation 718
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1056293944"
exon 721..819
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 721
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1433192968"
variation 722
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:374837913"
variation 723..724
/gene="SEMA4G"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1564794259"
variation 723
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:368885285"
variation 726
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1488741560"
variation 729
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850858994"
variation 734
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:759972554"
variation 735
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1311071149"
variation 736
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:765790226"
variation 738
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:371741444"
variation 739
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:756797401"
variation 741
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:941992758"
variation 742
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:145690277"
variation 743
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:750061929"
variation 744
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850859667"
variation 745
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564794293"
variation 750
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850859891"
variation 752
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1259506525"
variation 753
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:560293126"
variation 754..764
/gene="SEMA4G"
/replace="c"
/replace="cggctcaattc"
/db_xref="dbSNP:1850860190"
variation 754
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:893274055"
variation 755
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:749056930"
variation 756
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1370695015"
variation 760
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:768561807"
variation 766
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:779061181"
variation 768
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1432659738"
variation 770
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1589984551"
variation 771
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:921297403"
variation 772
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850860820"
variation 774
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:748069351"
variation 777
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850860959"
variation 778
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:376189318"
variation 782
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:932716016"
variation 784
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:751439655"
variation 786
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:772327550"
variation 791
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:572662465"
variation 792
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:760573069"
variation 793
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1406589169"
variation 795
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850861612"
variation 797
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1300897600"
variation 799
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133871074"
variation 801
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850861780"
variation 802
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1295606625"
variation 804
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1413321602"
variation 805..808
/gene="SEMA4G"
/replace="ct"
/replace="ctct"
/db_xref="dbSNP:1438510738"
variation 805
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1366536028"
variation 807
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850862143"
variation 810
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1400263197"
variation 815
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1340182509"
variation 816..817
/gene="SEMA4G"
/replace="ca"
/replace="caca"
/db_xref="dbSNP:764948073"
variation 817
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850862460"
variation 818
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850862536"
exon 820..913
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 820
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1004659697"
variation 822
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1205461904"
variation 828
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:746066448"
variation 829
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:770161568"
variation 830
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:149008935"
variation 836
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:764608308"
variation 840
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1446373763"
variation 845
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:887525390"
variation 847
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133873792"
variation 848
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:151095552"
variation 849
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:963256942"
variation 851
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:774709885"
variation 852
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:74154244"
variation 853
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:779530961"
variation 857
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:748582901"
variation 858
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:753596253"
variation 859
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1362954670"
variation 860
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1336829326"
variation 863..867
/gene="SEMA4G"
/replace="ag"
/replace="aggag"
/db_xref="dbSNP:768692347"
variation 864
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:374443024"
variation 865
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:752480989"
variation 867
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:758114685"
variation 869
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1215594471"
variation 871
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1564794890"
variation 872
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:758664453"
variation 877
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1326652882"
variation 879
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1316309086"
variation 880
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1198014436"
variation 887
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:746889193"
variation 889
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:140978394"
variation 890
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:201619012"
variation 892
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1589985904"
variation 893
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1236872889"
variation 896
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:934729093"
variation 901
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850892374"
variation 902
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850892457"
variation 906
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:746116241"
variation 907
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1420941687"
variation 908
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1477311108"
variation 910
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:769933802"
variation 912
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:775849846"
exon 914..1027
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 914
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1242205501"
variation 915
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850902998"
variation 918
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:749483446"
variation 919..920
/gene="SEMA4G"
/replace="g"
/replace="gg"
/db_xref="dbSNP:750452775"
variation 919
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:769114862"
variation 920
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1444498751"
variation 921
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:948989926"
variation 922
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1352712085"
variation 923
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1850903953"
variation 928
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:202220509"
variation 929
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:773841551"
variation 930
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:759183570"
variation 931
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:769395836"
variation 938
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:775330142"
variation 941
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:762461498"
variation 949
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:370387075"
variation 950
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:751241762"
variation 953
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1419465318"
variation 955..957
/gene="SEMA4G"
/replace="att"
/replace="attatt"
/db_xref="dbSNP:760677059"
variation 956
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564795185"
variation 957
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1589986519"
variation 964
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1393099586"
variation 965
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1589986527"
variation 966..979
/gene="SEMA4G"
/replace="ccgcc"
/replace="ccgccggagccgcc"
/db_xref="dbSNP:1392548033"
variation 967
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:188609242"
variation 968
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:375357185"
variation 970
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:200186312"
variation 971
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:756229401"
variation 973
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1375680753"
variation 974
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850905942"
variation 976
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:534321099"
variation 977
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:780089392"
variation 979
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:374506045"
variation 981
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1850906271"
variation 982
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1159156117"
variation 985
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:759497574"
variation 986
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1246356373"
variation 987
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:554197284"
variation 989
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:142527271"
variation 991..992
/gene="SEMA4G"
/replace=""
/replace="ct"
/db_xref="dbSNP:765930905"
variation 993
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:192790321"
variation 999
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:753223422"
variation 999
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133875208"
variation 1000..1005
/gene="SEMA4G"
/replace="gag"
/replace="gaggag"
/db_xref="dbSNP:1439037196"
variation 1002
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:755117958"
variation 1010
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:779341258"
variation 1011
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1181223858"
variation 1012
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1439657511"
variation 1015
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:954618111"
variation 1017
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1184542680"
variation 1024
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:748404181"
exon 1028..1197
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 1029
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:374767509"
variation 1031
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:369471768"
variation 1032
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:145899563"
variation 1034
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1319299438"
variation 1035
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:768211235"
variation 1040
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1461931758"
variation 1041
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1392770440"
variation 1047
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:562278554"
variation 1048
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:138710515"
variation 1053
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:772951663"
variation 1054
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:528948930"
variation 1057
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:760610802"
variation 1058
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:371666695"
variation 1059
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1178341036"
variation 1060
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1303651661"
variation 1064
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1208157981"
variation 1065
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:907505061"
variation 1068
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1316488117"
variation 1069
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:759573797"
variation 1075
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1465509378"
variation 1077
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:765335147"
variation 1078
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1452714855"
variation 1081
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1292595629"
variation 1086
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:752884133"
variation 1087
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:758650850"
variation 1089
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:940372860"
variation 1090..1092
/gene="SEMA4G"
/replace=""
/replace="gac"
/db_xref="dbSNP:1850922975"
variation 1093
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1297186803"
variation 1095
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1037811860"
variation 1100
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1356018019"
variation 1102
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1387941598"
variation 1104..1110
/gene="SEMA4G"
/replace="cttc"
/replace="cttcttc"
/db_xref="dbSNP:1298602317"
variation 1106
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1329808982"
variation 1107
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1233131910"
variation 1110
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:751912530"
variation 1112
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:540792779"
variation 1113
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:781655724"
variation 1117
/gene="SEMA4G"
/replace=""
/replace="c"
/db_xref="dbSNP:781528969"
variation 1117
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:898907623"
variation 1118
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:775552640"
variation 1125
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:754499823"
variation 1129
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:199950454"
variation 1131
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:142733326"
variation 1133
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850925211"
variation 1137
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133876712"
variation 1139
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1179175680"
variation 1141
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:771647101"
variation 1149
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1382158574"
variation 1150
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850925617"
variation 1156
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:773006606"
variation 1157
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:201790937"
variation 1159
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850926055"
variation 1161
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:919007889"
variation 1167..1184
/gene="SEMA4G"
/replace="ccgtgtggc"
/replace="ccgtgtggcccgtgtggc"
/db_xref="dbSNP:746431273"
variation 1167
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:868505946"
variation 1168
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:770726629"
variation 1169
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:551004768"
variation 1171
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1389345205"
variation 1172
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:759469028"
variation 1177..1190
/gene="SEMA4G"
/replace="cgtgtggctcgtgt"
/replace="cgtgtggctcgtgtggctcgtgt"
/db_xref="dbSNP:1850927374"
variation 1177
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:765262844"
variation 1178
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:377151700"
variation 1179
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:763278051"
variation 1182
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:764466706"
variation 1183
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:751824969"
variation 1186
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:888912092"
variation 1187
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1224011022"
variation 1188
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:118166648"
variation 1190
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:767904665"
variation 1196
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1850928191"
variation 1197
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1199366181"
exon 1198..1367
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 1198
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:2133877724"
variation 1199
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:200202967"
variation 1201
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:762050264"
variation 1203
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1170863177"
variation 1204
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133877770"
variation 1205
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:137857983"
variation 1206..1208
/gene="SEMA4G"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1850933595"
variation 1208
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:866490784"
variation 1210
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133877805"
variation 1211
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133877813"
variation 1212
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850933809"
variation 1214
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133877834"
variation 1215
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1238045368"
variation 1216
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133877862"
variation 1218
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:961966703"
variation 1219
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133877885"
variation 1221
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133877896"
variation 1223
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:1850934122"
variation 1223
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133877909"
variation 1225
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133877929"
variation 1226..1233
/gene="SEMA4G"
/replace="agaag"
/replace="agaagaag"
/db_xref="dbSNP:1179910574"
variation 1226
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133877937"
variation 1227
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:750733650"
variation 1228
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133877972"
variation 1229
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1850934544"
variation 1230
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:149549143"
variation 1231
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1850934768"
variation 1232
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133878008"
variation 1233
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:766970037"
variation 1234
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133878023"
variation 1235
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133878031"
variation 1238
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133878041"
variation 1239
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:144136150"
variation 1240
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133878063"
variation 1242
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133878069"
variation 1243
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850935025"
variation 1244
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:2133878084"
variation 1246
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133878090"
variation 1249
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133878099"
variation 1252
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:2133878106"
variation 1253
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133878118"
variation 1255
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:954409603"
variation 1256
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:374601814"
variation 1258
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:908122906"
variation 1260
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133878155"
variation 1261
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1329807522"
variation 1265
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133878172"
variation 1266
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564795878"
variation 1267
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133878196"
variation 1268
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:777213392"
variation 1269
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:751242836"
variation 1271
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133878218"
variation 1272
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133878227"
variation 1274
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133878231"
variation 1275
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:188155769"
variation 1277
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:138709087"
variation 1279
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:780858350"
variation 1280
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:141723515"
variation 1284
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:2133878282"
variation 1285
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850935891"
variation 1286
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:201040570"
variation 1287
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:200499542"
variation 1290
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1372311283"
variation 1291
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:576159833"
variation 1292
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:376301016"
variation 1296
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1413942825"
variation 1301
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850936462"
variation 1307
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:774536639"
variation 1311
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1313882295"
variation 1314
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1207707838"
variation 1318
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:943187702"
variation 1324
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:767392247"
variation 1325
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1161933809"
variation 1326
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:761950373"
variation 1327
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:772280066"
variation 1328
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:749963260"
variation 1329
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1235341225"
variation 1331
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:761169377"
variation 1333
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:766701174"
variation 1335
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:754363609"
variation 1336
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850937754"
variation 1339
/gene="SEMA4G"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1426443730"
variation 1341
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:759995340"
variation 1342
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:370799129"
variation 1352
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:755545765"
variation 1353
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:374213077"
variation 1354
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1420759299"
variation 1356
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1313225853"
variation 1357
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133878596"
variation 1359
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133878605"
variation 1360
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133878615"
variation 1362
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:146235728"
variation 1366
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:767264493"
exon 1368..1512
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 1368
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1473090285"
variation 1370
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:184755985"
variation 1372
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1589989813"
variation 1373
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:142303289"
variation 1374
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413764190"
variation 1375
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:200241224"
variation 1379
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1850976356"
variation 1381
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:764921000"
variation 1382
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1216318709"
variation 1383
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:752708818"
variation 1388
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:758200614"
variation 1390
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1161211887"
variation 1394
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1201341797"
variation 1396
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:369063086"
variation 1397
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:751695050"
variation 1399
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850977775"
variation 1400
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1187494537"
variation 1402
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1589989912"
variation 1405
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850978202"
variation 1408
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1264248737"
variation 1409
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1589989925"
variation 1413
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:964354750"
variation 1414
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1850978747"
variation 1419
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:190271357"
variation 1420
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1372385660"
variation 1422
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:757320010"
variation 1424
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:376797424"
variation 1425
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850979346"
variation 1426
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:150824972"
variation 1427
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1240413142"
variation 1428
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1193173688"
variation 1430
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1399753855"
variation 1433
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850979819"
variation 1434
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1433937750"
variation 1435..1437
/gene="SEMA4G"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1452660752"
variation 1435
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:780443579"
variation 1437
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:367883776"
variation 1440
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:770163597"
variation 1442
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1342003827"
variation 1450
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1397546136"
variation 1451
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:372466257"
variation 1452
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850980546"
variation 1453
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:749809765"
variation 1455
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:376969087"
variation 1457
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850980816"
variation 1459
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1229991911"
variation 1460..1462
/gene="SEMA4G"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:35989286"
variation 1460
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1339531318"
variation 1462
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:988692457"
variation 1463
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:774913495"
variation 1465
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:199762950"
variation 1466
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:553537753"
variation 1469
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850981685"
variation 1470
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:776474084"
variation 1472
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:759217416"
variation 1474
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1261099304"
variation 1475
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:199677082"
variation 1477
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1200907162"
variation 1478
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:752375155"
variation 1482
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:577628245"
variation 1484
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:764005138"
variation 1485
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:751463430"
variation 1486
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:781196938"
variation 1488
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:750677818"
variation 1489
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1390825588"
variation 1491
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1388071510"
variation 1493
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850983227"
variation 1494
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:756226933"
variation 1495
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:965691185"
variation 1500
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1365199089"
variation 1501
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:949989449"
variation 1502
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:147630038"
variation 1511
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:749676557"
variation 1512
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:768865327"
exon 1513..1735
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 1513
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:775053317"
variation 1522
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850994061"
variation 1524..1525
/gene="SEMA4G"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1564796771"
variation 1526
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1850994366"
variation 1529
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:748920327"
variation 1531
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:761554973"
variation 1532
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:774063487"
variation 1536
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850994826"
variation 1537
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:761753573"
variation 1547
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:917222193"
variation 1552
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1850995253"
variation 1554
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1210217429"
variation 1555
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1354888744"
variation 1556
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1564796809"
variation 1557..1563
/gene="SEMA4G"
/replace=""
/replace="agacttg"
/db_xref="dbSNP:1564796818"
variation 1558
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:767502487"
variation 1560
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:773129383"
variation 1563
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:760713409"
variation 1564
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1203491941"
variation 1565
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:766463475"
variation 1571
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850996705"
variation 1572
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1471143694"
variation 1573
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:754033511"
variation 1574
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850996981"
variation 1576
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1290463761"
variation 1578
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:755190563"
variation 1581
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:765708793"
variation 1587
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:971229127"
variation 1590..1618
/gene="SEMA4G"
/replace="gttg"
/replace="gttgcacccactgatggctcggcccgttg"
/db_xref="dbSNP:1850997601"
variation 1591
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:753167511"
variation 1594
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:979985262"
variation 1596
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1221818105"
variation 1597
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1371460605"
variation 1598..1601
/gene="SEMA4G"
/replace=""
/replace="cact"
/db_xref="dbSNP:1422220691"
variation 1599
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:758828192"
variation 1600
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:778460071"
variation 1607
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850998242"
variation 1608
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1170412118"
variation 1609
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1330018610"
variation 1610
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:199635372"
variation 1613
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:779575501"
variation 1614
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:565104337"
variation 1615
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:201564489"
variation 1616
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1400651750"
variation 1617
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850999005"
variation 1618
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:778525725"
variation 1620
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:748004748"
variation 1621
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1213885536"
variation 1627
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:149116714"
variation 1628
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:371636173"
variation 1633
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:367801117"
variation 1634
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:770950663"
variation 1635
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1589990995"
variation 1638
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:889294061"
variation 1644
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1182151325"
variation 1648
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:776709167"
variation 1651
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:759518723"
variation 1652
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:76584327"
variation 1655
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:143118773"
variation 1657
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1186433901"
variation 1660
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:150071842"
variation 1661
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:764503702"
variation 1666
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851000938"
variation 1668
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1345529789"
variation 1669
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:752037569"
variation 1670
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133884735"
variation 1672
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851001443"
variation 1674
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:757714467"
variation 1676
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:779441290"
variation 1677
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1316183503"
variation 1686
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851001826"
variation 1688
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851001929"
variation 1689..1694
/gene="SEMA4G"
/replace="cac"
/replace="caccac"
/db_xref="dbSNP:755502387"
variation 1694
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:147741050"
variation 1695
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851002277"
variation 1707
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:199671205"
variation 1709
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:553260640"
variation 1711
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:1851002597"
variation 1712
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:747781429"
variation 1717
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1231751585"
variation 1718
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1457264028"
variation 1719
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1564797032"
variation 1720
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851003219"
variation 1722
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133884897"
variation 1725
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564797037"
variation 1726
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:771880296"
variation 1728
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851003533"
variation 1732
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1354200251"
exon 1736..1851
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 1736
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851018889"
variation 1737
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:750865022"
variation 1742
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:754532026"
variation 1747
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1302211133"
variation 1749
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1564797210"
variation 1752
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1458448137"
variation 1754
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:201540929"
variation 1755
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:752382102"
variation 1758
/gene="SEMA4G"
/replace="c"
/replace="cctac"
/db_xref="dbSNP:1851020664"
variation 1758
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:7901675"
variation 1759
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:144844358"
variation 1763
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1427873810"
variation 1764
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:542169408"
variation 1765
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:781235374"
variation 1767
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:200666280"
variation 1768
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1400944443"
variation 1769
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1425740385"
variation 1772
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564797257"
variation 1775
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:770024953"
variation 1776
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:775644707"
variation 1779
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:147919269"
variation 1780
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851022799"
variation 1782
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1735148329"
variation 1787
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:372822376"
variation 1790
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:962692236"
variation 1794
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:377379944"
variation 1797
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133886261"
variation 1798
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851023312"
variation 1799
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:762280561"
variation 1802
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1009845265"
variation 1803
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851023747"
variation 1806
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:767751429"
variation 1807
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1384559788"
variation 1809
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:773734788"
variation 1812
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1340727081"
variation 1813
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133886347"
variation 1815
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1661076286"
variation 1816
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1253166327"
variation 1818
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1197875859"
variation 1819
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:761134082"
variation 1821..1824
/gene="SEMA4G"
/replace="tg"
/replace="tgtg"
/db_xref="dbSNP:1851024692"
variation 1822
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1437655804"
variation 1823
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:764733748"
variation 1824
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:752147128"
variation 1835
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:757896884"
variation 1837
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1307458129"
variation 1838..1844
/gene="SEMA4G"
/replace="tctct"
/replace="tctctct"
/db_xref="dbSNP:1187347525"
variation 1838
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1424188963"
variation 1845
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:763844803"
variation 1846
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:377270509"
variation 1851
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1395507326"
exon 1852..2027
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 1853
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:200163492"
variation 1854
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:773503586"
variation 1855
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1316773436"
variation 1857
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:761187011"
variation 1861
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1235416443"
variation 1863
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1306051543"
variation 1866
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:766932360"
variation 1867
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1353345900"
variation 1868
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:777088467"
variation 1870
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1191733049"
variation 1871
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1261588998"
variation 1873
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:762570919"
variation 1874
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1203475590"
variation 1876
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:763459869"
variation 1878
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:141233234"
variation 1879
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:778175945"
variation 1882
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851035626"
variation 1885
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:113498503"
variation 1887
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1453643880"
variation 1890
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133887370"
variation 1895
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:755967370"
variation 1898
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1367220882"
variation 1899
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:200695967"
variation 1902
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851036004"
variation 1908
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1365187139"
variation 1909
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1450944219"
variation 1910
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:962865221"
variation 1912
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:780182850"
variation 1913
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:147992447"
variation 1914
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1453337360"
variation 1918
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:140692272"
variation 1919
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:778822733"
variation 1921
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133887521"
variation 1927
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851036845"
variation 1931
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1328594140"
variation 1932
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1564797582"
variation 1937
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1442804873"
variation 1939
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:748411182"
variation 1940
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851037376"
variation 1943
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851037479"
variation 1945
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:772130257"
variation 1946
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1307898484"
variation 1951
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1449228698"
variation 1953
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:770900988"
variation 1955
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851038019"
variation 1956
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1318990634"
variation 1958
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1236915123"
variation 1961
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1260199125"
variation 1963
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851038517"
variation 1964
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851038668"
variation 1965
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:777961396"
variation 1967
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:747411614"
variation 1968
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1251127577"
variation 1969
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1382570602"
variation 1971
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:771261070"
variation 1972
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:371386076"
variation 1976
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:756576170"
variation 1977
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:759917226"
variation 1979
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:768215640"
variation 1981
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1180693559"
variation 1982
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1417942007"
variation 1986
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:780011724"
variation 1987
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:761371562"
variation 1989
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133887829"
variation 1990
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1392930732"
variation 1993
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851041113"
variation 1994
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1461216948"
variation 2000
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:767343866"
variation 2001
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:750070570"
variation 2002
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1389861288"
variation 2004
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1229597463"
variation 2006
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:760597640"
variation 2007
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:912639818"
variation 2008
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:984794076"
variation 2012
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:766227835"
variation 2016
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:7905266"
variation 2017
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1305237666"
variation 2019..2021
/gene="SEMA4G"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1851042581"
variation 2019
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:754808483"
variation 2021
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:779066804"
variation 2023
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133888012"
variation 2024
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133888016"
variation 2025
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:925424123"
variation 2027
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:752779759"
exon 2028..2089
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 2028
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851052204"
variation 2031
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:138772734"
variation 2034
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851052415"
variation 2035
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:375633368"
variation 2036
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1358635527"
variation 2037..2053
/gene="SEMA4G"
/replace="ga"
/replace="gatacaggacatagaga"
/db_xref="dbSNP:1435619713"
variation 2039
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1271640141"
variation 2042
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:764114736"
variation 2043
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:995770723"
variation 2048
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851053214"
variation 2049..2056
/gene="SEMA4G"
/replace="agag"
/replace="agagagag"
/db_xref="dbSNP:767881320"
variation 2050
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1325570015"
variation 2052
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:190201835"
variation 2053
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851053643"
variation 2055
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851053737"
variation 2061
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:538842540"
variation 2062
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851053925"
variation 2063
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:757411949"
variation 2067
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133889080"
variation 2071
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:781378063"
variation 2072
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:746282456"
variation 2074
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1231622802"
variation 2075
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1279237287"
variation 2077
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:756467836"
variation 2079
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:369529769"
variation 2082
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851054882"
variation 2084
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:534283434"
exon 2090..3216
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 2090
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1169802472"
variation 2093
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133910482"
variation 2095
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1358850075"
variation 2099
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:761133475"
variation 2100
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1191685942"
variation 2101
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851322719"
variation 2103
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:565832622"
variation 2104
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1301023166"
variation 2106
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1238599331"
variation 2107
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:140873008"
variation 2108..2111
/gene="SEMA4G"
/replace="atat"
/replace="atatat"
/db_xref="dbSNP:1180219371"
variation 2109
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:775161961"
variation 2110
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851323614"
variation 2112
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1435583593"
variation 2113
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1347264509"
variation 2119
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:755490675"
variation 2120
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1022174562"
variation 2121
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851324366"
variation 2123
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1282490941"
variation 2132
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1232746478"
variation 2134
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851325083"
variation 2140..2142
/gene="SEMA4G"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1564801111"
variation 2140
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1015510000"
variation 2143
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:551143626"
variation 2145
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1309192746"
variation 2146
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1446522565"
variation 2147
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851326399"
variation 2149
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1313501848"
variation 2151
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851326936"
variation 2152
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851327156"
variation 2154
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1381487456"
variation 2160
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1370845164"
variation 2169
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1212785459"
variation 2170
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:962694375"
variation 2171
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851328377"
variation 2174
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:11591349"
variation 2175
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:536866327"
variation 2176
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1250348904"
variation 2180
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1447859281"
variation 2181
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1186203566"
variation 2182
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:977649336"
variation 2185
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133911153"
variation 2189
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:756712868"
variation 2192
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1204147027"
variation 2193
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:556345883"
variation 2194
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1434047317"
variation 2196
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851330601"
variation 2198
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1173815254"
variation 2199
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:567995095"
variation 2200
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:986972740"
variation 2203
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1322261528"
variation 2209
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1386272160"
variation 2210
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1468467340"
variation 2211
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851331669"
variation 2212
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:745459702"
variation 2214
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:755937099"
variation 2215
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851332127"
variation 2218
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242453332"
variation 2219
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:11190780"
variation 2220
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1369013608"
variation 2224
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1217004954"
variation 2226
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:749061715"
variation 2234
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1323427412"
variation 2235
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:768679541"
variation 2236
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:562213978"
variation 2239
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1463832678"
variation 2240
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1215245125"
variation 2242
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1392099800"
variation 2245
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1247539943"
variation 2246
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851334603"
variation 2248
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1489476783"
variation 2249
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851335052"
variation 2254
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:774150942"
variation 2255
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1330576370"
variation 2256
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:554180516"
variation 2257
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1161357971"
variation 2258
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1222920929"
variation 2263..2267
/gene="SEMA4G"
/replace="ct"
/replace="cttct"
/db_xref="dbSNP:1409419478"
variation 2266..2270
/gene="SEMA4G"
/replace="ct"
/replace="ctcct"
/db_xref="dbSNP:1399901647"
variation 2271
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851337089"
variation 2272
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1164988814"
variation 2274
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1347204536"
variation 2277..2281
/gene="SEMA4G"
/replace="tt"
/replace="ttctt"
/db_xref="dbSNP:1851337943"
variation 2279
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1351283007"
variation 2281
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851338509"
variation 2287
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:748317224"
variation 2290
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1301958846"
variation 2294
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851339309"
variation 2299
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1350650732"
variation 2300
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:771987099"
variation 2301
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:909015462"
variation 2302
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:947024954"
variation 2304
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1348931588"
variation 2320
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1044109678"
variation 2321
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851341027"
variation 2329
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851341287"
variation 2333
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851341554"
variation 2335
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1223598937"
variation 2338
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:941896553"
variation 2344
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1590003340"
variation 2345..2348
/gene="SEMA4G"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:749161619"
variation 2345
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:867056759"
variation 2347
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851342959"
variation 2348
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1341846221"
variation 2352
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1323698735"
variation 2355
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1219725456"
variation 2356
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:897779980"
variation 2357
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1483432059"
variation 2359
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:766759551"
variation 2360
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133912160"
variation 2362
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1398820091"
variation 2365
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:938445182"
variation 2366
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1249568875"
variation 2368..2370
/gene="SEMA4G"
/replace="t"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:1564801421"
variation 2376
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851345504"
variation 2378
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851345730"
variation 2380
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133912278"
variation 2382..2384
/gene="SEMA4G"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:34661749"
variation 2382
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1469396700"
variation 2384
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1590003500"
variation 2387
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1051674712"
variation 2388
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1473643656"
variation 2389
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415748001"
variation 2395
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1403242646"
variation 2397
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851347694"
variation 2398
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851347910"
variation 2399
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413115744"
variation 2403
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1186071819"
variation 2404
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1162547813"
variation 2405
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1370560535"
variation 2411
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:889128459"
variation 2412
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851348837"
variation 2413
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1431132181"
variation 2418..2426
/gene="SEMA4G"
/replace="ctcc"
/replace="ctcccctcc"
/db_xref="dbSNP:1310336433"
variation 2420
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851349496"
variation 2421
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1056944101"
variation 2424
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851350086"
variation 2426
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:886274992"
variation 2428
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1828080527"
variation 2431..2437
/gene="SEMA4G"
/replace="cct"
/replace="ccttcct"
/db_xref="dbSNP:1442168150"
variation 2431
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1285150909"
variation 2432
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:150176473"
variation 2435
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1284040676"
variation 2440
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1243979563"
variation 2442
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1454985511"
variation 2446
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1016127185"
variation 2447
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1342914307"
variation 2448
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1207413139"
variation 2451
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1272637340"
variation 2453..2458
/gene="SEMA4G"
/replace=""
/replace="atcagc"
/db_xref="dbSNP:1437134295"
variation 2453
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:546548368"
variation 2456..2465
/gene="SEMA4G"
/replace=""
/replace="agcctcccca"
/db_xref="dbSNP:1232285107"
variation 2459
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851353656"
variation 2460
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851353903"
variation 2461..2464
/gene="SEMA4G"
/replace="ccc"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1851354331"
variation 2461
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:999055334"
variation 2462..2466
/gene="SEMA4G"
/replace="c"
/replace="cccac"
/db_xref="dbSNP:1188248769"
variation 2463
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:558511473"
variation 2465
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851355064"
variation 2466
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1471688492"
variation 2467..2468
/gene="SEMA4G"
/replace=""
/replace="gtgtga"
/db_xref="dbSNP:1279740182"
variation 2467
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564801584"
variation 2468
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1182551535"
variation 2474
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1390425592"
variation 2475
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:866465441"
variation 2477
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:899127927"
variation 2478
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851356441"
variation 2484..2485
/gene="SEMA4G"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1851356699"
variation 2489..2491
/gene="SEMA4G"
/replace="t"
/replace="tat"
/db_xref="dbSNP:776469814"
variation 2489
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:1564801613"
variation 2490
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:995448141"
variation 2491
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1406943937"
variation 2492..2497
/gene="SEMA4G"
/replace="gaga"
/replace="gagaga"
/db_xref="dbSNP:1031921038"
variation 2493
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1352660512"
variation 2494
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1166136937"
variation 2496
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:960318556"
variation 2500
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851358185"
variation 2505
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1217254719"
variation 2508
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:993082702"
variation 2509
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851358464"
variation 2510
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851358683"
variation 2512
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:576676078"
variation 2513
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851359112"
variation 2515
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:954125817"
variation 2516
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1409881469"
variation 2521
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1590004029"
variation 2522
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1335465291"
variation 2523
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1361197103"
variation 2525
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1450956457"
variation 2531
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1314573273"
variation 2532
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242083934"
variation 2534..2535
/gene="SEMA4G"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1366179476"
variation 2534
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851361189"
variation 2536
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1734059355"
variation 2537..2540
/gene="SEMA4G"
/replace="aaca"
/replace="aacaaca"
/db_xref="dbSNP:398114688"
variation 2538..2545
/gene="SEMA4G"
/replace="acac"
/replace="acacacac"
/db_xref="dbSNP:146737296"
variation 2538
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851362081"
variation 2540
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1470152414"
variation 2541
/gene="SEMA4G"
/replace=""
/replace="c"
/db_xref="dbSNP:1554885387"
variation 2543..2546
/gene="SEMA4G"
/replace="c"
/replace="cacc"
/db_xref="dbSNP:1564801730"
variation 2543
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:980911684"
variation 2551
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:908989869"
variation 2552
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1318120156"
variation 2555
/gene="SEMA4G"
/replace=""
/replace="a"
/db_xref="dbSNP:1851363694"
variation 2556
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1297128475"
variation 2557..2558
/gene="SEMA4G"
/replace=""
/replace="at"
/db_xref="dbSNP:201653131"
variation 2558
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851363979"
variation 2559
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:941859324"
variation 2561
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1275426272"
variation 2567
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:544003449"
variation 2574
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:561580399"
variation 2579
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:987306998"
variation 2580
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1761267634"
variation 2586
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851365080"
variation 2587
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:760046546"
variation 2590
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851365638"
variation 2598
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:570837619"
variation 2600
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851366097"
variation 2601
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1461145737"
variation 2602
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:956410819"
variation 2606
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1172757131"
variation 2607
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590004294"
variation 2611
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:765696472"
variation 2612..2619
/gene="SEMA4G"
/replace="ctgt"
/replace="ctgtctgt"
/db_xref="dbSNP:1851367609"
variation 2612
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851367435"
variation 2614
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:776736066"
variation 2626
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:541757083"
variation 2627
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1455911411"
variation 2629
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133914046"
variation 2631
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:947649741"
variation 2632
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:540658889"
variation 2637
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1458477096"
variation 2639
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851368804"
variation 2654
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:979738620"
variation 2655
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133914138"
variation 2656
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1419920691"
variation 2674
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851369510"
variation 2677
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:926970920"
variation 2679
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:938406307"
variation 2686
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1345587818"
variation 2691..2699
/gene="SEMA4G"
/replace="ggatg"
/replace="ggatggatg"
/db_xref="dbSNP:1156991738"
variation 2692
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1590004435"
variation 2697
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1411538590"
variation 2698
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1447292211"
variation 2699
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1057292576"
variation 2709
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1401448436"
variation 2710
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:148889377"
variation 2712
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1354019972"
variation 2715
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1357855929"
variation 2716
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:185501392"
variation 2717
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1437149072"
variation 2718
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1393859490"
variation 2721
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1314077837"
variation 2725..2726
/gene="SEMA4G"
/replace="c"
/replace="cc"
/db_xref="dbSNP:745620184"
variation 2731
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851373532"
variation 2732
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1357883329"
variation 2734
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1058101"
variation 2735..2739
/gene="SEMA4G"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1564801889"
variation 2736
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1043523463"
variation 2738
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1440759734"
variation 2739
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1037520890"
variation 2740
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851374834"
variation 2746
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851375125"
variation 2750
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851375359"
variation 2755..2759
/gene="SEMA4G"
/replace="tc"
/replace="tcctc"
/db_xref="dbSNP:1851375586"
variation 2756
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1287105200"
variation 2757
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:899075093"
variation 2759
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851376270"
variation 2760
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:758453345"
variation 2761
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:999022475"
variation 2763
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:533032857"
variation 2765
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851377123"
variation 2770
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851377286"
variation 2772..2780
/gene="SEMA4G"
/replace="gggaaaggg"
/replace="gggaaagggggaaaggg"
/db_xref="dbSNP:1237569905"
variation 2772
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1276666015"
variation 2778
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851377980"
variation 2779..2785
/gene="SEMA4G"
/replace="ggag"
/replace="ggaggag"
/db_xref="dbSNP:1212458091"
variation 2785
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:539958411"
variation 2791
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1031806643"
variation 2793
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:996061169"
variation 2794..2798
/gene="SEMA4G"
/replace="tgtct"
/replace="tgtctgtct"
/db_xref="dbSNP:1851379088"
variation 2794..2796
/gene="SEMA4G"
/replace="t"
/replace="tgt"
/db_xref="dbSNP:1851378916"
variation 2795
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1276056518"
variation 2796
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1318520975"
variation 2799
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851379758"
variation 2802
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1028300853"
variation 2803
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1222315298"
variation 2808
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:145456828"
variation 2810
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851380461"
variation 2814
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1259577119"
variation 2815
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851380817"
variation 2816
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851380992"
variation 2822
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:969446661"
variation 2826
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851381422"
variation 2830
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1313689869"
variation 2831
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851381840"
variation 2834
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851382067"
variation 2840
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:980495734"
variation 2842
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1016423976"
variation 2844
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851382772"
variation 2848
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:764283941"
variation 2849
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851383229"
variation 2850
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851383454"
variation 2851
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:889784981"
variation 2852
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851383892"
variation 2857
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851384118"
variation 2858
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1482005638"
variation 2859
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1008277694"
variation 2860
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:751801892"
variation 2866
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133915301"
variation 2871
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1590004825"
variation 2874
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851385217"
variation 2875..2876
/gene="SEMA4G"
/replace=""
/replace="ct"
/db_xref="dbSNP:971792769"
variation 2875
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851385462"
variation 2876
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:919060865"
variation 2878
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851386135"
variation 2887
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851386346"
variation 2888
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1365943648"
variation 2889
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1160574437"
variation 2890
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:549901293"
variation 2891
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851387327"
variation 2892
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:987778470"
variation 2894
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:956145941"
variation 2898
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1189614913"
variation 2899
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1484440106"
variation 2903
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851388353"
variation 2904
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851388576"
variation 2905
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:722435"
variation 2907
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851389219"
variation 2908
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133915599"
variation 2910
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1174615834"
variation 2912
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1377821148"
variation 2913
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1486785377"
variation 2915
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851390176"
variation 2917
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851390425"
variation 2918
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1021817552"
variation 2922
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851390914"
variation 2926
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1258766345"
variation 2927
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:13114"
variation 2929
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:530575708"
variation 2936
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1322070191"
variation 2937
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851392002"
variation 2939
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851392246"
variation 2941
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590005004"
variation 2943
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851392702"
variation 2947
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1294208197"
variation 2950
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851393161"
variation 2955
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:796584525"
variation 2956
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851393640"
variation 2959
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1443718900"
variation 2960
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:549209014"
variation 2961..2965
/gene="SEMA4G"
/replace="ccccc"
/replace="cccccc"
/db_xref="dbSNP:1851394245"
variation 2963
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851394479"
variation 2965
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851394644"
variation 2966
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1272765213"
variation 2967
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:535391514"
variation 2970
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133915982"
variation 2974
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:722434"
variation 2975
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:756150215"
variation 2976
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851395747"
variation 2978..2986
/gene="SEMA4G"
/replace="tga"
/replace="tgaggatga"
/db_xref="dbSNP:1851395903"
variation 2981
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1287595742"
variation 2983
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1590005102"
variation 2984..2989
/gene="SEMA4G"
/replace="tg"
/replace="tgactg"
/db_xref="dbSNP:1282127784"
variation 2988..2990
/gene="SEMA4G"
/replace="t"
/replace="tgt"
/db_xref="dbSNP:1851396880"
variation 2989
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851397104"
variation 2992
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851397297"
variation 2993
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851397538"
variation 2998
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851397765"
variation 3002
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1453577215"
variation 3003
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851398062"
variation 3004
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1339982424"
variation 3009
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:992545494"
variation 3010
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1473984676"
variation 3014
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:377579383"
variation 3017
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1193217573"
variation 3021
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1429752865"
variation 3022
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:535979784"
variation 3024
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851399630"
variation 3025
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1053207362"
variation 3032
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1204475752"
variation 3037
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1468760178"
variation 3040
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851400265"
variation 3041
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:895968520"
variation 3048
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:547453410"
variation 3049
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1215821939"
variation 3052
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1014460178"
variation 3054
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851401422"
variation 3057
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1272754894"
variation 3061
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590005244"
variation 3064
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:566052365"
variation 3065
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1228291159"
variation 3066
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:539856889"
variation 3067..3074
/gene="SEMA4G"
/replace="aatg"
/replace="aatgaatg"
/db_xref="dbSNP:1851402794"
variation 3070
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1294126122"
variation 3073
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:1245235656"
variation 3074
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1023629686"
variation 3083
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:907599520"
variation 3084
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851403820"
variation 3085
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1194666457"
variation 3087
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1459569804"
variation 3090
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851404319"
variation 3093
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1397200065"
variation 3096
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1006217092"
variation 3098
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851405001"
variation 3102
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:940472396"
variation 3106
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1370830712"
variation 3107
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851405676"
variation 3110
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851405873"
variation 3112
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851406098"
variation 3115
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564802346"
variation 3118
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1168572915"
variation 3122
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1454629864"
variation 3126
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851406807"
variation 3132
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1015896546"
variation 3133
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1183846917"
variation 3134
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1590005486"
variation 3135..3136
/gene="SEMA4G"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1851407769"
variation 3135
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1037468969"
variation 3136
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1267016453"
variation 3137
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851408064"
variation 3139
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:971763006"
variation 3140
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:780109310"
variation 3150
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851408894"
variation 3153
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:920446283"
variation 3155
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1590005630"
variation 3156..3161
/gene="SEMA4G"
/replace="ggggag"
/replace="ggggagggggag"
/db_xref="dbSNP:1851409933"
variation 3156
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1026045787"
variation 3157
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1249625499"
variation 3161
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1397803701"
variation 3162
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851410880"
variation 3164
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:11190781"
variation 3165
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851411332"
variation 3167
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:375892284"
variation 3174
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590005760"
variation 3176
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851412105"
variation 3177
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:1348958879"
variation 3177
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590005788"
variation 3180
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1441105677"
variation 3181
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:890411724"
variation 3182
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133917246"
variation 3183
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1008640180"
variation 3184
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:576811967"
variation 3185..3186
/gene="SEMA4G"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1851413621"
variation 3186
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:537243928"
variation 3187
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:555966416"
variation 3188
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:573637014"
variation 3190
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:934667679"
variation 3191
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1171676783"
regulatory 3194..3199
/regulatory_class="polyA_signal_sequence"
/gene="SEMA4G"
/note="hexamer: AATAAA"
variation 3202
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:866768376"
variation 3203
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1010346124"
variation 3204
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851414998"
variation 3205
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851415299"
variation 3209
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:917372450"
variation 3210..3213
/gene="SEMA4G"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1439739794"
variation 3211
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590006249"
variation 3213
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851416502"
polyA_site 3216
/gene="SEMA4G"
/note="major polyA site"
ORIGIN
aaaacggacctcagaaaaccaggactagctctactgtcgggggcagggtgaccccatcagtaacctacaacccctctagaacttcacaactccctctcaccatggagtttgcatttgatgcagaaaggcatgtgatccctccctccttctgacctcttagctggggattccatggccacacaaccctgtgactccatgtccccccgattccaggaccccccatggccccatgattccttgactcctatgaccttatgacccctgaccttccaagtgacttccttggactttgacccctgtgactgtgcttcccattccccgcccccacaacctgtgactctggctccctttgggggtcttgttagtctgggcctccccaggaagatgtgggggaggctctggcccctcctcctcagcatcctcacagcaactgcagtcccaggaccctcactgcggagaccgtctagagaactagatgccacccctcggatgaccataccctatgaagagctctctgggacccggcacttcaagggccaagcccagaactactcaacactgctgctggaggaggcctcagcaaggctgctggtgggagcccgaggtgccctgttctctctcagtgccaacgacataggagatggggctcacaaagagatccactgggaagcctccccagagatgcaaagcaaatgtcatcaaaaagggaaaaacaaccagacggagtgctttaaccatgtgcggttcctgcagcggctcaattctacccacctctatgcatgtgggactcacgccttccagcccctctgtgcagccattgatgctgaggccttcaccttgccaaccagcttcgaggaggggaaggagaagtgtccttatgacccagcccgtggcttcacaggcctcatcattgatggaggcctctacacagccactaggtatgaattccggagcattcctgacatccgccggagccgccacccacactccctgagaactgaggagacaccaatgcattggctcaatgatgcggagtttgtgttctccgtcctcgtgcgggagagcaaggccagtgcagtgggtgatgatgacaaggtgtactacttcttcacggagcgtgccactgaggagggctctggcagcttcactcagagccgcagcagtcaccgtgtggcccgtgtggctcgtgtctgcaagggagacctgggagggaagaagatcctgcagaagaagtggacttccttcctgaaagcccgtctcatctgccacattccactgtatgagacactgcgtggggtctgcagcctggatgctgaaacctcaagccgtacacacttctatgcagccttcacgctgagcacacagtggaagaccctggaggcctcagccatctgccgctatgacctggcagagatccaggctgtctttgcaggaccctatatggaataccaggatggttcccggcgctggggtcgctatgagggtggggtgcctgagccccggcctggctcgtgtatcacagattcattgcgcagccaaggctacaattcatcccaagacttgccatccctggtcctggactttgtaaagttgcacccactgatggctcggcccgttgtgcccacacgtggacggcccctgctgctcaagcgcaacatacgctacacacaccttacagggacacctgtcaccacgcctgctggacctacctatgacctgctctttctgggcacagctgatggctggatccacaaggccgtagtcctgggctctgggatgcacattattgaagagacacaagtgttcagggagtcccagtctgtggaaaatctagtcatctctctattgcagcacagcctctatgtgggggctcctagcggagtcatccagctaccactctccagctgctcccgctaccgatcctgctatgactgcatcttggcccgagacccctactgtggctgggaccctggcacccatgcctgcgcagcagccaccaccatagccaacaggtcccagggaagcaggacagcactgatacaggacatagagagaggaaatcgaggctgtgagagcagcagggatacaggcagggctctgcaggtccatatgggctcaatgtcaccaccctctgcatggccctgtgtgctggatggtcctgaaaccagacaagacctctgccagccacctaagccctgcgtacattcacatgcacacatggaagaatgtttatcggctgggctgcagtgcccccaccctcaccttctcctggtgcattcttgtttcatccctgcttctggacttggggtaccctcccaattgccacatcctatctggtcctcttccccagccccatgtggtgacctctttgtcaagagcttgggaacgggccagcctggggaggtaagactgcatcactcccctcctctcccttcctgtgtggcccttgtgaatcagcctccccactctccttggtcattctcaagagtatgagagacagagctccaggcatgtcccatccccatgcacatgtggtaacacacacctgtatcacacatgtgcttacatttccactcacatgcacctctgagcctcccttgctgtcttggacctgtctgttgggtttagtccgtggacatttcagagggagatccccctcccatttaactgtcctcacaggcccttgcctaggatggatgaccaacactgcactcaatgagccagcctctcttttgggggaatcaagcatttgcttcctctagactacagcagggaaagggaggagaaatctgatgtctcaactggcacatgaagcccattcttggaactatgcaaagggcagaggctgggagtttggacgcttagctcctacccctgtcctacctcaccggggcactttcaggggccaggggcctctgaagtctctaggcctatatgggacaatcaattctgactgagctcccccattcccctcgggtgaggatgactgttatttttgtagctgagaacgtggaatcccacgggtttttactgcccttcacccaacctctcccacctccaccccacaatgaatgtatttattgtgagaatggctacacttctttaggaatgcccccacttacaaccaggtgggtggaacaggcatgtgacagagtggggagcctgggctcagctcctccccctgccgttggttaataaacaccctttttccccacaaaaaaaaaaaaaaa
//
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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