ver.2
Home
|
Help
|
Advanced search
Previous release (v1)
2024-04-30 14:04:25, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NR_172053 3977 bp RNA linear PRI 27-JUN-2023
DEFINITION Homo sapiens semaphorin 4G (SEMA4G), transcript variant 5,
non-coding RNA.
ACCESSION NR_172053
VERSION NR_172053.1
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 3977)
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 3977)
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 3977)
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 3977)
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 3977)
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 3977)
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 3977)
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 3977)
AUTHORS Holtmaat AJ, De Winter F, De Wit J, Gorter JA, da Silva FH and
Verhaagen J.
TITLE Semaphorins: contributors to structural stability of hippocampal
networks?
JOURNAL Prog Brain Res 138, 17-38 (2002)
PUBMED 12432760
REMARK Review article
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from AL133215.17.
Summary: Semaphorins are a large family of conserved secreted and
membrane associated proteins which possess a semaphorin (Sema)
domain and a PSI domain (found in plexins, semaphorins and
integrins) in the N-terminal extracellular portion. Based on
sequence and structural similarities, semaphorins are put into
eight classes: invertebrates contain classes 1 and 2, viruses have
class V, and vertebrates contain classes 3-7. Semaphorins serve as
axon guidance ligands via multimeric receptor complexes, some (if
not all) containing plexin proteins. Multiple transcript variants
encoding different isoforms have been found for this gene.
[provided by RefSeq, Feb 2011].
##Evidence-Data-START##
RNAseq introns :: single sample supports all introns SAMEA1968540,
SAMEA2142348 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: full length.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-88 AL133215.17 52328-52415
89-231 AL133215.17 55718-55860
232-380 AL133215.17 55953-56101
381-443 AL133215.17 56371-56433
444-542 AL133215.17 60456-60554
543-636 AL133215.17 61119-61212
637-750 AL133215.17 61351-61464
751-920 AL133215.17 61673-61842
921-1090 AL133215.17 61926-62095
1091-1235 AL133215.17 62672-62816
1236-1458 AL133215.17 62946-63168
1459-1574 AL133215.17 63402-63517
1575-1735 AL133215.17 63646-63806
1736-1797 AL133215.17 63992-64053
1798-2850 AL133215.17 66129-67181
2851-3977 AL133215.17 67314-68440
FEATURES Location/Qualifiers
source 1..3977
/organism="Homo sapiens"
/mol_type="transcribed RNA"
/db_xref="taxon:9606"
/chromosome="10"
/map="10q24.31"
gene 1..3977
/gene="SEMA4G"
/note="semaphorin 4G"
/db_xref="GeneID:57715"
/db_xref="HGNC:HGNC:10735"
/db_xref="MIM:618991"
misc_RNA 1..3977
/gene="SEMA4G"
/product="semaphorin 4G, transcript variant 5"
/db_xref="GeneID:57715"
/db_xref="HGNC:HGNC:10735"
/db_xref="MIM:618991"
exon 1..88
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 1..2
/gene="SEMA4G"
/replace=""
/replace="ag"
/db_xref="dbSNP:1467940472"
variation 1
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1194222240"
variation 2
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1253674040"
variation 3
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1375312685"
variation 4
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850567705"
variation 5
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1479078047"
variation 6
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1296202088"
variation 7
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:991345198"
variation 8
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133849907"
variation 10
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1408262006"
variation 11
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850567967"
variation 12
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1370130694"
variation 13..14
/gene="SEMA4G"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1589975880"
variation 13
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1589975877"
variation 14
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133849925"
variation 17
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1174345519"
variation 22..29
/gene="SEMA4G"
/replace="cagctggt"
/replace="cagctggtcagctggt"
/db_xref="dbSNP:1419154452"
variation 26
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850568268"
variation 27
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1410747126"
variation 28
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:866504226"
variation 30
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1436737403"
variation 32
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1393334579"
variation 33..41
/gene="SEMA4G"
/replace="gtggggccg"
/replace="gtggggccgtggggccg"
/db_xref="dbSNP:1850568583"
variation 35..38
/gene="SEMA4G"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:2133849963"
variation 39
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1005296035"
variation 42
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850568737"
variation 44
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850568792"
variation 45
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133849980"
variation 46
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850568859"
variation 47
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850568916"
variation 48..53
/gene="SEMA4G"
/replace="cg"
/replace="cgcgcg"
/db_xref="dbSNP:1850569061"
variation 48
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:917174896"
variation 50
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1175789338"
variation 53
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1392762963"
variation 63
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1461341188"
variation 64
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850569329"
variation 65
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1212560086"
variation 66
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850569479"
variation 68
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1589975902"
variation 71
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850569628"
variation 72
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850569699"
variation 73
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:546087970"
variation 75
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1254875583"
variation 78
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:982522207"
variation 79
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1332295021"
variation 80
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133850056"
variation 81
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850570085"
variation 82
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850570148"
variation 83
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:557633516"
variation 84
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850570281"
variation 85
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:374064553"
variation 86
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:922120937"
variation 87
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133850081"
exon 89..231
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 89
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1010644581"
variation 95
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1430821467"
variation 99
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850672377"
variation 104
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1402602510"
misc_feature 108..2624
/gene="SEMA4G"
/inference="COORDINATES:
alignment:Blast2seq::RefSeq|NM_001393925.1"
/note="primary ORF has stop codon >50 nucleotides from the
terminal splice site; nonsense-mediated decay (NMD)
candidate"
variation 108
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1191397762"
variation 110
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1344292943"
variation 111..134
/gene="SEMA4G"
/replace=""
/replace="tgggggaggctctggcccctcctc"
/db_xref="dbSNP:1564791884"
variation 112..116
/gene="SEMA4G"
/replace="ggggg"
/replace="gggggg"
/db_xref="dbSNP:1850672932"
variation 112
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:745907076"
variation 113
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:769754047"
variation 116
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850673074"
variation 122
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1393022504"
variation 125
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:775751808"
variation 127
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1043525758"
variation 128
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1167174298"
variation 137
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850673445"
variation 142
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:1850673633"
variation 142
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:763127413"
variation 146
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:141766082"
variation 147
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1850673834"
variation 148
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1469347701"
variation 150
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:201769907"
variation 151
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1363910803"
variation 153
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850674227"
variation 154
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:762257142"
variation 156
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850674430"
variation 157
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:768000743"
variation 158
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:753300939"
variation 159
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:765633702"
variation 161
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:528334576"
variation 169
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:764810125"
variation 170
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1322465491"
variation 172
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:752448070"
variation 175
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1261974981"
variation 177
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:150563616"
variation 178
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:751304450"
variation 179
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133857417"
variation 180
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850675630"
variation 183
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1195652118"
variation 184
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:139918504"
variation 185
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:571547734"
variation 186
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850676089"
variation 189
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850676178"
variation 192
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1202124518"
variation 194
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133857469"
variation 197
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:532192623"
variation 198
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:780081656"
variation 200
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:2133857483"
variation 202
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:867204232"
variation 203
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1159955320"
variation 210
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:749532175"
variation 211
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:768824226"
variation 214
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1850677171"
variation 216
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850677263"
variation 219
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:774700812"
variation 222
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:369789414"
variation 225
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:962113918"
variation 226..229
/gene="SEMA4G"
/replace="a"
/replace="atga"
/db_xref="dbSNP:1406530664"
variation 226
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:772310279"
variation 227
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1344402684"
variation 228
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378220105"
variation 229
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133857555"
exon 232..380
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 238
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:369353258"
variation 245
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:144341151"
variation 246
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:372839640"
variation 247
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1370809407"
variation 249
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:780136613"
variation 255
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:913597081"
variation 258
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:749297787"
variation 261
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1441420061"
variation 265
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:755205395"
variation 266
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850682502"
variation 269
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1360751746"
variation 275
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850682665"
variation 277
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1248834281"
variation 279
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850682797"
variation 280
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850682873"
variation 281
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1284517077"
variation 282
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:779253360"
variation 285
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:748287481"
variation 287
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1205748549"
variation 290..297
/gene="SEMA4G"
/replace="ggagg"
/replace="ggaggagg"
/db_xref="dbSNP:1850683258"
variation 291
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1234802535"
variation 294
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:199970914"
variation 296
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:756103359"
variation 301
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:747581175"
variation 305
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850683769"
variation 308
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1029721556"
variation 312
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1243856800"
variation 314
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1446315165"
variation 319
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:376810147"
variation 320
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1384733681"
variation 321
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1384572205"
variation 324
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:750643700"
variation 325
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:202147105"
variation 328
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1007038634"
variation 329
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1589978805"
variation 331
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1352343381"
variation 332
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1402573417"
variation 337..344
/gene="SEMA4G"
/replace="tctctc"
/replace="tctctctc"
/db_xref="dbSNP:1441071018"
variation 339
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850685194"
variation 340
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:199688982"
variation 342
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850685355"
variation 346
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:762606692"
variation 353
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:146573432"
variation 354
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:140040145"
variation 362
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1445693261"
variation 365
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850685679"
variation 367
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:761353685"
variation 368
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1387484882"
variation 369
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1056746530"
variation 373
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:373053309"
variation 376
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:750147136"
variation 378
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:760612775"
exon 381..443
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 386
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:765388169"
variation 387
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1385079315"
variation 393
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:200094625"
variation 395
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:879452513"
variation 396
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:752650927"
variation 397..400
/gene="SEMA4G"
/replace="c"
/replace="cccc"
/db_xref="dbSNP:1589979126"
variation 398
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:149776999"
variation 401
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:891205288"
variation 404
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1423146487"
variation 408
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850694572"
variation 414..416
/gene="SEMA4G"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1457139894"
variation 414
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1257694646"
variation 419
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:751823274"
variation 422
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1224318002"
variation 424..428
/gene="SEMA4G"
/replace="aaaaa"
/replace="aaaaaa"
/db_xref="dbSNP:769978574"
variation 424
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:757731950"
variation 425
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:368462093"
variation 432
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1221941297"
variation 437
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1274539366"
variation 439
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:746403415"
variation 441
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1056293944"
exon 444..542
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 444
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1433192968"
variation 445
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:374837913"
variation 446..447
/gene="SEMA4G"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1564794259"
variation 446
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:368885285"
variation 449
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1488741560"
variation 452
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850858994"
variation 457
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:759972554"
variation 458
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1311071149"
variation 459
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:765790226"
variation 461
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:371741444"
variation 462
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:756797401"
variation 464
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:941992758"
variation 465
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:145690277"
variation 466
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:750061929"
variation 467
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850859667"
variation 468
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564794293"
variation 473
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850859891"
variation 475
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1259506525"
variation 476
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:560293126"
variation 477..487
/gene="SEMA4G"
/replace="c"
/replace="cggctcaattc"
/db_xref="dbSNP:1850860190"
variation 477
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:893274055"
variation 478
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:749056930"
variation 479
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1370695015"
variation 483
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:768561807"
variation 489
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:779061181"
variation 491
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1432659738"
variation 493
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1589984551"
variation 494
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:921297403"
variation 495
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850860820"
variation 497
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:748069351"
variation 500
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850860959"
variation 501
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:376189318"
variation 505
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:932716016"
variation 507
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:751439655"
variation 509
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:772327550"
variation 514
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:572662465"
variation 515
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:760573069"
variation 516
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1406589169"
variation 518
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850861612"
variation 520
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1300897600"
variation 522
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133871074"
variation 524
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850861780"
variation 525
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1295606625"
variation 527
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1413321602"
variation 528..531
/gene="SEMA4G"
/replace="ct"
/replace="ctct"
/db_xref="dbSNP:1438510738"
variation 528
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1366536028"
variation 530
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850862143"
variation 533
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1400263197"
variation 538
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1340182509"
variation 539..540
/gene="SEMA4G"
/replace="ca"
/replace="caca"
/db_xref="dbSNP:764948073"
variation 540
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850862460"
variation 541
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850862536"
exon 543..636
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 543
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1004659697"
variation 545
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1205461904"
variation 551
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:746066448"
variation 552
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:770161568"
variation 553
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:149008935"
variation 559
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:764608308"
variation 563
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1446373763"
variation 568
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:887525390"
variation 570
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133873792"
variation 571
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:151095552"
variation 572
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:963256942"
variation 574
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:774709885"
variation 575
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:74154244"
variation 576
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:779530961"
variation 580
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:748582901"
variation 581
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:753596253"
variation 582
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1362954670"
variation 583
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1336829326"
variation 586..590
/gene="SEMA4G"
/replace="ag"
/replace="aggag"
/db_xref="dbSNP:768692347"
variation 587
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:374443024"
variation 588
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:752480989"
variation 590
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:758114685"
variation 592
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1215594471"
variation 594
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1564794890"
variation 595
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:758664453"
variation 600
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1326652882"
variation 602
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1316309086"
variation 603
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1198014436"
variation 610
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:746889193"
variation 612
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:140978394"
variation 613
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:201619012"
variation 615
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1589985904"
variation 616
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1236872889"
variation 619
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:934729093"
variation 624
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850892374"
variation 625
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850892457"
variation 629
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:746116241"
variation 630
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1420941687"
variation 631
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1477311108"
variation 633
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:769933802"
variation 635
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:775849846"
exon 637..750
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 637
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1242205501"
variation 638
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850902998"
variation 641
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:749483446"
variation 642..643
/gene="SEMA4G"
/replace="g"
/replace="gg"
/db_xref="dbSNP:750452775"
variation 642
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:769114862"
variation 643
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1444498751"
variation 644
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:948989926"
variation 645
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1352712085"
variation 646
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1850903953"
variation 651
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:202220509"
variation 652
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:773841551"
variation 653
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:759183570"
variation 654
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:769395836"
variation 661
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:775330142"
variation 664
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:762461498"
variation 672
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:370387075"
variation 673
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:751241762"
variation 676
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1419465318"
variation 678..680
/gene="SEMA4G"
/replace="att"
/replace="attatt"
/db_xref="dbSNP:760677059"
variation 679
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564795185"
variation 680
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1589986519"
variation 687
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1393099586"
variation 688
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1589986527"
variation 689..702
/gene="SEMA4G"
/replace="ccgcc"
/replace="ccgccggagccgcc"
/db_xref="dbSNP:1392548033"
variation 690
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:188609242"
variation 691
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:375357185"
variation 693
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:200186312"
variation 694
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:756229401"
variation 696
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1375680753"
variation 697
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850905942"
variation 699
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:534321099"
variation 700
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:780089392"
variation 702
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:374506045"
variation 704
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1850906271"
variation 705
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1159156117"
variation 708
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:759497574"
variation 709
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1246356373"
variation 710
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:554197284"
variation 712
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:142527271"
variation 714..715
/gene="SEMA4G"
/replace=""
/replace="ct"
/db_xref="dbSNP:765930905"
variation 716
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:192790321"
variation 722
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:753223422"
variation 722
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133875208"
variation 723..728
/gene="SEMA4G"
/replace="gag"
/replace="gaggag"
/db_xref="dbSNP:1439037196"
variation 725
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:755117958"
variation 733
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:779341258"
variation 734
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1181223858"
variation 735
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1439657511"
variation 738
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:954618111"
variation 740
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1184542680"
variation 747
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:748404181"
exon 751..920
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 752
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:374767509"
variation 754
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:369471768"
variation 755
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:145899563"
variation 757
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1319299438"
variation 758
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:768211235"
variation 763
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1461931758"
variation 764
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1392770440"
variation 770
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:562278554"
variation 771
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:138710515"
variation 776
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:772951663"
variation 777
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:528948930"
variation 780
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:760610802"
variation 781
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:371666695"
variation 782
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1178341036"
variation 783
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1303651661"
variation 787
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1208157981"
variation 788
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:907505061"
variation 791
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1316488117"
variation 792
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:759573797"
variation 798
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1465509378"
variation 800
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:765335147"
variation 801
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1452714855"
variation 804
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1292595629"
variation 809
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:752884133"
variation 810
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:758650850"
variation 812
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:940372860"
variation 813..815
/gene="SEMA4G"
/replace=""
/replace="gac"
/db_xref="dbSNP:1850922975"
variation 816
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1297186803"
variation 818
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1037811860"
variation 823
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1356018019"
variation 825
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1387941598"
variation 827..833
/gene="SEMA4G"
/replace="cttc"
/replace="cttcttc"
/db_xref="dbSNP:1298602317"
variation 829
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1329808982"
variation 830
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1233131910"
variation 833
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:751912530"
variation 835
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:540792779"
variation 836
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:781655724"
variation 840
/gene="SEMA4G"
/replace=""
/replace="c"
/db_xref="dbSNP:781528969"
variation 840
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:898907623"
variation 841
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:775552640"
variation 848
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:754499823"
variation 852
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:199950454"
variation 854
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:142733326"
variation 856
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850925211"
variation 860
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133876712"
variation 862
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1179175680"
variation 864
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:771647101"
variation 872
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1382158574"
variation 873
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850925617"
variation 879
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:773006606"
variation 880
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:201790937"
variation 882
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850926055"
variation 884
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:919007889"
variation 890..907
/gene="SEMA4G"
/replace="ccgtgtggc"
/replace="ccgtgtggcccgtgtggc"
/db_xref="dbSNP:746431273"
variation 890
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:868505946"
variation 891
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:770726629"
variation 892
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:551004768"
variation 894
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1389345205"
variation 895
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:759469028"
variation 900..913
/gene="SEMA4G"
/replace="cgtgtggctcgtgt"
/replace="cgtgtggctcgtgtggctcgtgt"
/db_xref="dbSNP:1850927374"
variation 900
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:765262844"
variation 901
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:377151700"
variation 902
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:763278051"
variation 905
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:764466706"
variation 906
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:751824969"
variation 909
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:888912092"
variation 910
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1224011022"
variation 911
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:118166648"
variation 913
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:767904665"
variation 919
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1850928191"
variation 920
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1199366181"
exon 921..1090
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 921
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:2133877724"
variation 922
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:200202967"
variation 924
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:762050264"
variation 926
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1170863177"
variation 927
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133877770"
variation 928
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:137857983"
variation 929..931
/gene="SEMA4G"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1850933595"
variation 931
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:866490784"
variation 933
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133877805"
variation 934
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133877813"
variation 935
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850933809"
variation 937
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133877834"
variation 938
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1238045368"
variation 939
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133877862"
variation 941
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:961966703"
variation 942
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133877885"
variation 944
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133877896"
variation 946
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:1850934122"
variation 946
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133877909"
variation 948
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133877929"
variation 949..956
/gene="SEMA4G"
/replace="agaag"
/replace="agaagaag"
/db_xref="dbSNP:1179910574"
variation 949
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133877937"
variation 950
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:750733650"
variation 951
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133877972"
variation 952
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1850934544"
variation 953
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:149549143"
variation 954
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1850934768"
variation 955
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133878008"
variation 956
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:766970037"
variation 957
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133878023"
variation 958
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133878031"
variation 961
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133878041"
variation 962
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:144136150"
variation 963
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133878063"
variation 965
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133878069"
variation 966
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850935025"
variation 967
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:2133878084"
variation 969
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133878090"
variation 972
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133878099"
variation 975
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:2133878106"
variation 976
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133878118"
variation 978
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:954409603"
variation 979
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:374601814"
variation 981
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:908122906"
variation 983
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133878155"
variation 984
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1329807522"
variation 988
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133878172"
variation 989
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564795878"
variation 990
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133878196"
variation 991
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:777213392"
variation 992
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:751242836"
variation 994
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133878218"
variation 995
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133878227"
variation 997
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133878231"
variation 998
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:188155769"
variation 1000
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:138709087"
variation 1002
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:780858350"
variation 1003
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:141723515"
variation 1007
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:2133878282"
variation 1008
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850935891"
variation 1009
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:201040570"
variation 1010
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:200499542"
variation 1013
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1372311283"
variation 1014
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:576159833"
variation 1015
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:376301016"
variation 1019
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1413942825"
variation 1024
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850936462"
variation 1030
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:774536639"
variation 1034
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1313882295"
variation 1037
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1207707838"
variation 1041
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:943187702"
variation 1047
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:767392247"
variation 1048
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1161933809"
variation 1049
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:761950373"
variation 1050
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:772280066"
variation 1051
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:749963260"
variation 1052
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1235341225"
variation 1054
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:761169377"
variation 1056
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:766701174"
variation 1058
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:754363609"
variation 1059
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850937754"
variation 1062
/gene="SEMA4G"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1426443730"
variation 1064
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:759995340"
variation 1065
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:370799129"
variation 1075
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:755545765"
variation 1076
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:374213077"
variation 1077
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1420759299"
variation 1079
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1313225853"
variation 1080
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:2133878596"
variation 1082
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133878605"
variation 1083
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133878615"
variation 1085
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:146235728"
variation 1089
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:767264493"
exon 1091..1235
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 1091
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1473090285"
variation 1093
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:184755985"
variation 1095
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1589989813"
variation 1096
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:142303289"
variation 1097
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413764190"
variation 1098
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:200241224"
variation 1102
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1850976356"
variation 1104
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:764921000"
variation 1105
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1216318709"
variation 1106
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:752708818"
variation 1111
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:758200614"
variation 1113
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1161211887"
variation 1117
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1201341797"
variation 1119
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:369063086"
variation 1120
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:751695050"
variation 1122
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850977775"
variation 1123
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1187494537"
variation 1125
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1589989912"
variation 1128
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850978202"
variation 1131
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1264248737"
variation 1132
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1589989925"
variation 1136
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:964354750"
variation 1137
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1850978747"
variation 1142
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:190271357"
variation 1143
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1372385660"
variation 1145
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:757320010"
variation 1147
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:376797424"
variation 1148
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850979346"
variation 1149
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:150824972"
variation 1150
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1240413142"
variation 1151
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1193173688"
variation 1153
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1399753855"
variation 1156
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1850979819"
variation 1157
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1433937750"
variation 1158..1160
/gene="SEMA4G"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1452660752"
variation 1158
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:780443579"
variation 1160
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:367883776"
variation 1163
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:770163597"
variation 1165
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1342003827"
variation 1173
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1397546136"
variation 1174
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:372466257"
variation 1175
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850980546"
variation 1176
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:749809765"
variation 1178
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:376969087"
variation 1180
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850980816"
variation 1182
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1229991911"
variation 1183..1185
/gene="SEMA4G"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:35989286"
variation 1183
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1339531318"
variation 1185
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:988692457"
variation 1186
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:774913495"
variation 1188
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:199762950"
variation 1189
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:553537753"
variation 1192
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850981685"
variation 1193
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:776474084"
variation 1195
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:759217416"
variation 1197
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1261099304"
variation 1198
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:199677082"
variation 1200
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1200907162"
variation 1201
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:752375155"
variation 1205
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:577628245"
variation 1207
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:764005138"
variation 1208
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:751463430"
variation 1209
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:781196938"
variation 1211
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:750677818"
variation 1212
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1390825588"
variation 1214
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1388071510"
variation 1216
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850983227"
variation 1217
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:756226933"
variation 1218
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:965691185"
variation 1223
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1365199089"
variation 1224
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:949989449"
variation 1225
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:147630038"
variation 1234
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:749676557"
variation 1235
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:768865327"
exon 1236..1458
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 1236
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:775053317"
variation 1245
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850994061"
variation 1247..1248
/gene="SEMA4G"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1564796771"
variation 1249
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1850994366"
variation 1252
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:748920327"
variation 1254
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:761554973"
variation 1255
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:774063487"
variation 1259
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850994826"
variation 1260
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:761753573"
variation 1270
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:917222193"
variation 1275
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1850995253"
variation 1277
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1210217429"
variation 1278
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1354888744"
variation 1279
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1564796809"
variation 1280..1286
/gene="SEMA4G"
/replace=""
/replace="agacttg"
/db_xref="dbSNP:1564796818"
variation 1281
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:767502487"
variation 1283
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:773129383"
variation 1286
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:760713409"
variation 1287
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1203491941"
variation 1288
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:766463475"
variation 1294
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850996705"
variation 1295
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1471143694"
variation 1296
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:754033511"
variation 1297
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1850996981"
variation 1299
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1290463761"
variation 1301
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:755190563"
variation 1304
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:765708793"
variation 1310
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:971229127"
variation 1313..1341
/gene="SEMA4G"
/replace="gttg"
/replace="gttgcacccactgatggctcggcccgttg"
/db_xref="dbSNP:1850997601"
variation 1314
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:753167511"
variation 1317
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:979985262"
variation 1319
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1221818105"
variation 1320
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1371460605"
variation 1321..1324
/gene="SEMA4G"
/replace=""
/replace="cact"
/db_xref="dbSNP:1422220691"
variation 1322
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:758828192"
variation 1323
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:778460071"
variation 1330
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1850998242"
variation 1331
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1170412118"
variation 1332
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1330018610"
variation 1333
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:199635372"
variation 1336
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:779575501"
variation 1337
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:565104337"
variation 1338
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:201564489"
variation 1339
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1400651750"
variation 1340
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1850999005"
variation 1341
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:778525725"
variation 1343
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:748004748"
variation 1344
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1213885536"
variation 1350
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:149116714"
variation 1351
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:371636173"
variation 1356
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:367801117"
variation 1357
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:770950663"
variation 1358
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1589990995"
variation 1361
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:889294061"
variation 1367
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1182151325"
variation 1371
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:776709167"
variation 1374
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:759518723"
variation 1375
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:76584327"
variation 1378
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:143118773"
variation 1380
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1186433901"
variation 1383
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:150071842"
variation 1384
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:764503702"
variation 1389
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851000938"
variation 1391
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1345529789"
variation 1392
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:752037569"
variation 1393
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133884735"
variation 1395
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851001443"
variation 1397
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:757714467"
variation 1399
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:779441290"
variation 1400
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1316183503"
variation 1409
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851001826"
variation 1411
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851001929"
variation 1412..1417
/gene="SEMA4G"
/replace="cac"
/replace="caccac"
/db_xref="dbSNP:755502387"
variation 1417
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:147741050"
variation 1418
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851002277"
variation 1430
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:199671205"
variation 1432
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:553260640"
variation 1434
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:1851002597"
variation 1435
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:747781429"
variation 1440
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1231751585"
variation 1441
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1457264028"
variation 1442
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1564797032"
variation 1443
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851003219"
variation 1445
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133884897"
variation 1448
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564797037"
variation 1449
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:771880296"
variation 1451
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851003533"
variation 1455
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1354200251"
exon 1459..1574
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 1459
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851018889"
variation 1460
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:750865022"
variation 1465
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:754532026"
variation 1470
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1302211133"
variation 1472
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1564797210"
variation 1475
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1458448137"
variation 1477
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:201540929"
variation 1478
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:752382102"
variation 1481
/gene="SEMA4G"
/replace="c"
/replace="cctac"
/db_xref="dbSNP:1851020664"
variation 1481
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:7901675"
variation 1482
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:144844358"
variation 1486
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1427873810"
variation 1487
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:542169408"
variation 1488
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:781235374"
variation 1490
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:200666280"
variation 1491
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1400944443"
variation 1492
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1425740385"
variation 1495
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564797257"
variation 1498
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:770024953"
variation 1499
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:775644707"
variation 1502
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:147919269"
variation 1503
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851022799"
variation 1505
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1735148329"
variation 1510
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:372822376"
variation 1513
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:962692236"
variation 1517
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:377379944"
variation 1520
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133886261"
variation 1521
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851023312"
variation 1522
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:762280561"
variation 1525
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1009845265"
variation 1526
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851023747"
variation 1529
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:767751429"
variation 1530
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1384559788"
variation 1532
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:773734788"
variation 1535
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1340727081"
variation 1536
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133886347"
variation 1538
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1661076286"
variation 1539
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1253166327"
variation 1541
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1197875859"
variation 1542
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:761134082"
variation 1544..1547
/gene="SEMA4G"
/replace="tg"
/replace="tgtg"
/db_xref="dbSNP:1851024692"
variation 1545
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1437655804"
variation 1546
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:764733748"
variation 1547
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:752147128"
variation 1558
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:757896884"
variation 1560
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1307458129"
variation 1561..1567
/gene="SEMA4G"
/replace="tctct"
/replace="tctctct"
/db_xref="dbSNP:1187347525"
variation 1561
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1424188963"
variation 1568
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:763844803"
variation 1569
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:377270509"
variation 1574
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1395507326"
exon 1575..1735
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 1576
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:200163492"
variation 1577
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:773503586"
variation 1578
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1316773436"
variation 1580
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:761187011"
variation 1584
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1235416443"
variation 1586
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1306051543"
variation 1589
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:766932360"
variation 1590
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1353345900"
variation 1591
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:777088467"
variation 1593
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1191733049"
variation 1594
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1261588998"
variation 1596
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:762570919"
variation 1597
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1203475590"
variation 1599
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:763459869"
variation 1601
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:141233234"
variation 1602
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:778175945"
variation 1605
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851035626"
variation 1608
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:113498503"
variation 1610
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1453643880"
variation 1613
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133887370"
variation 1618
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:755967370"
variation 1621
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1367220882"
variation 1622
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:200695967"
variation 1625
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851036004"
variation 1631
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1365187139"
variation 1632
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1450944219"
variation 1633
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:962865221"
variation 1635
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:780182850"
variation 1636
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:147992447"
variation 1637
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1453337360"
variation 1641
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:140692272"
variation 1642
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:778822733"
variation 1644
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133887521"
variation 1650
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851036845"
variation 1654
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1328594140"
variation 1655
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1564797582"
variation 1660
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1442804873"
variation 1662
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:748411182"
variation 1663
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851037376"
variation 1666
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851037479"
variation 1668
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:772130257"
variation 1669
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1307898484"
variation 1674
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1449228698"
variation 1676
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:770900988"
variation 1678
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851038019"
variation 1679
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1318990634"
variation 1681
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1236915123"
variation 1684
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1260199125"
variation 1686
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851038517"
variation 1687
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851038668"
variation 1688
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:777961396"
variation 1690
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:747411614"
variation 1691
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1251127577"
variation 1692
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1382570602"
variation 1694
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:771261070"
variation 1695
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:371386076"
variation 1699
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:756576170"
variation 1700
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:759917226"
variation 1702
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:768215640"
variation 1704
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1180693559"
variation 1705
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1417942007"
variation 1709
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:780011724"
variation 1710
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:761371562"
variation 1712
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133887829"
variation 1713
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1392930732"
variation 1716
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851041113"
variation 1717
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1461216948"
variation 1723
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:767343866"
variation 1724
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:750070570"
variation 1725
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1389861288"
variation 1727
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1229597463"
variation 1729
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:760597640"
variation 1730
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:912639818"
variation 1731
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:984794076"
variation 1735
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:766227835"
exon 1736..1797
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 1736
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851052204"
variation 1739
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:138772734"
variation 1742
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851052415"
variation 1743
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:375633368"
variation 1744
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1358635527"
variation 1745..1761
/gene="SEMA4G"
/replace="ga"
/replace="gatacaggacatagaga"
/db_xref="dbSNP:1435619713"
variation 1747
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1271640141"
variation 1750
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:764114736"
variation 1751
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:995770723"
variation 1756
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851053214"
variation 1757..1764
/gene="SEMA4G"
/replace="agag"
/replace="agagagag"
/db_xref="dbSNP:767881320"
variation 1758
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1325570015"
variation 1760
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:190201835"
variation 1761
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851053643"
variation 1763
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851053737"
variation 1769
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:538842540"
variation 1770
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851053925"
variation 1771
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:757411949"
variation 1775
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133889080"
variation 1779
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:781378063"
variation 1780
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:746282456"
variation 1782
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1231622802"
variation 1783
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1279237287"
variation 1785
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:756467836"
variation 1787
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:369529769"
variation 1790
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851054882"
variation 1792
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:534283434"
exon 1798..2850
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 1798
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1373085610"
variation 1799
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851211935"
variation 1800..1812
/gene="SEMA4G"
/replace="ccaccaccac"
/replace="ccaccaccaccac"
/replace="ccaccaccaccaccac"
/db_xref="dbSNP:145835827"
variation 1800..1801
/gene="SEMA4G"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1554884798"
variation 1802
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1334008977"
variation 1806
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1327563265"
variation 1808
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851212995"
variation 1812..1814
/gene="SEMA4G"
/replace=""
/replace="ctg"
/db_xref="dbSNP:755081302"
variation 1816
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:552270687"
variation 1819
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1341977736"
variation 1820
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1235282106"
variation 1821
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1282755788"
variation 1822
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:754085049"
variation 1827
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1589998314"
variation 1830
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1199969523"
variation 1833
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:760031264"
variation 1834
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:753257306"
variation 1836
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133901396"
variation 1837
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:773478369"
variation 1838
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:778125924"
variation 1843
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:570573396"
variation 1845
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1175068535"
variation 1850
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:755545892"
variation 1853
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:779730408"
variation 1855
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1158667773"
variation 1858
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:748889973"
variation 1859
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1384413039"
variation 1862
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:768472015"
variation 1863
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:761068926"
variation 1866
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1442105033"
variation 1867
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851217451"
variation 1868
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851217575"
variation 1870
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1305846909"
variation 1871
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:183718929"
variation 1872
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1232869244"
variation 1874
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:549851109"
variation 1877
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1245506254"
variation 1878
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1353024006"
variation 1881
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:146245319"
variation 1882
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:760851566"
variation 1883
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851218914"
variation 1884
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851219065"
variation 1886
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:770897727"
variation 1888
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1195301504"
variation 1889
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1264768450"
variation 1892
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:777019767"
variation 1894
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:759761969"
variation 1895
/gene="SEMA4G"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1005161073"
variation 1896
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:201001972"
variation 1900
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1451010139"
variation 1901
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851220823"
variation 1906
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1157499811"
variation 1908
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:776051888"
variation 1909
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851221493"
variation 1910
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1005716850"
variation 1911
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851222036"
variation 1915
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851222273"
variation 1916
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1017136365"
variation 1918
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:763219828"
variation 1919
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:764701072"
variation 1920
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:137971825"
variation 1922
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:755671543"
variation 1924
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851223790"
variation 1925
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851224022"
variation 1926
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1355476316"
variation 1927
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1589998686"
variation 1928..1930
/gene="SEMA4G"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1251708384"
variation 1928
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:977978033"
variation 1929
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:765835066"
variation 1930
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851225605"
variation 1931
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1589998724"
variation 1934
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:753494547"
variation 1935
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1315808916"
variation 1937
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1287605179"
variation 1938
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:149389232"
variation 1939
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:144727154"
variation 1940
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851227514"
variation 1943
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:748043373"
variation 1945
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851228007"
variation 1946
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:148516703"
variation 1947
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:374200198"
variation 1949
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851228915"
variation 1952
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:142773171"
variation 1953
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:147237913"
variation 1961
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851229807"
variation 1962
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:141030743"
variation 1964
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851230304"
variation 1967
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851230541"
variation 1970..1971
/gene="SEMA4G"
/replace=""
/replace="tg"
/db_xref="dbSNP:1851230987"
variation 1970
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851230778"
variation 1971
/gene="SEMA4G"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1851231197"
variation 1973
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:770205655"
variation 1976
/gene="SEMA4G"
/replace=""
/replace="g"
/db_xref="dbSNP:1851231852"
variation 1976
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851231625"
variation 1977..1978
/gene="SEMA4G"
/replace=""
/replace="aa"
/db_xref="dbSNP:1851232419"
variation 1977
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:775542275"
variation 1978
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851232649"
variation 1979
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851232858"
variation 1980
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851233038"
variation 1980
/gene="SEMA4G"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1851233269"
variation 1982
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851233489"
variation 1991
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:755113434"
variation 1992
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:764316566"
variation 1997
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:774952582"
variation 2000
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133902664"
variation 2003
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:762161081"
variation 2005
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1298897763"
variation 2008
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851235035"
variation 2009
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:765887043"
variation 2010
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:753406520"
variation 2011
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1408024389"
variation 2015
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851235974"
variation 2018
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:754482102"
variation 2019
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1307475986"
variation 2021
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:764912089"
variation 2022
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:539263557"
variation 2023
/gene="SEMA4G"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1851237219"
variation 2025
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:866091256"
variation 2026
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:558586100"
variation 2027
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:777395006"
variation 2028
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1589998968"
variation 2029
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851238350"
variation 2030
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851238569"
variation 2031
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1049622681"
variation 2032
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:746976668"
variation 2033
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:940882437"
variation 2039
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:757318232"
variation 2042
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851239938"
variation 2044
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851240164"
variation 2045
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1444392472"
variation 2047
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1204049997"
variation 2048
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851240875"
variation 2051
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:977211113"
variation 2053
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851241278"
variation 2054
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1257594428"
variation 2057
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1486401615"
variation 2058
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:781268916"
variation 2059
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:144879682"
variation 2060
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1423563944"
variation 2061
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851242706"
variation 2064
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1171588564"
variation 2066..2068
/gene="SEMA4G"
/replace="cac"
/replace="cacac"
/db_xref="dbSNP:1392472908"
variation 2069
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851243412"
variation 2073
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:902133075"
variation 2075
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851243897"
variation 2077
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851244159"
variation 2079
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851244380"
variation 2085
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851244630"
variation 2088
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1168271228"
variation 2089
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1376084022"
variation 2091
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1416703361"
variation 2094
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:775801456"
variation 2100
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1378378322"
variation 2101
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:997799025"
variation 2102
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851245990"
variation 2105
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:749431067"
variation 2106
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1339881664"
variation 2110
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1031887205"
variation 2112
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:769068051"
variation 2114
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1589999247"
variation 2115
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:774521972"
variation 2116
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1207455851"
variation 2117
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:762152467"
variation 2118
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:772635727"
variation 2119
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851247954"
variation 2120..2124
/gene="SEMA4G"
/replace="tg"
/replace="tgatg"
/db_xref="dbSNP:1187659489"
variation 2120
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851248197"
variation 2121
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851248500"
variation 2123
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851248659"
variation 2124
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:957195278"
variation 2129
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1589999321"
variation 2130
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851249179"
variation 2131
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:759100020"
variation 2132
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1448113201"
variation 2133
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851249681"
variation 2134
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:990022918"
variation 2136
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1395953506"
variation 2137
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:544195173"
variation 2138
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851250291"
variation 2140
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:752430522"
variation 2142
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1358691563"
variation 2147
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1224493460"
variation 2151
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1454241106"
variation 2152
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1265325492"
variation 2153..2157
/gene="SEMA4G"
/replace="c"
/replace="cgcgc"
/db_xref="dbSNP:1851251239"
variation 2153
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:147942823"
variation 2154
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:140546736"
variation 2155
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:751374543"
variation 2156..2157
/gene="SEMA4G"
/replace=""
/replace="tata"
/db_xref="dbSNP:1851251846"
variation 2156
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:757083877"
variation 2159
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1589999484"
variation 2160
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:149914326"
variation 2161
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:750335846"
variation 2170..2185
/gene="SEMA4G"
/replace="gcctcatcctggcctc"
/replace="gcctcatcctggcctcatcctggcctc"
/db_xref="dbSNP:1851252713"
variation 2170
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1380369416"
variation 2172
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:756293264"
variation 2174
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:779930213"
variation 2178
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851253195"
variation 2182
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:939406010"
variation 2183
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:749539011"
variation 2184
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1270578063"
variation 2185
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:71488078"
variation 2186
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851254045"
variation 2188
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:768819125"
variation 2190
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:144937502"
variation 2194..2196
/gene="SEMA4G"
/replace=""
/replace="tct"
/db_xref="dbSNP:569204913"
variation 2197
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:748554644"
variation 2198
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851254882"
variation 2199
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1210510722"
variation 2202
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:887229636"
variation 2203
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:772406976"
variation 2204
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851255424"
variation 2210
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851255543"
variation 2211
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:773734595"
variation 2212
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:761134134"
variation 2215
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851256014"
variation 2217
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:769355889"
variation 2218
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:774916385"
variation 2223
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:542184127"
variation 2224
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1326312908"
variation 2225
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851256871"
variation 2227
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:763691852"
variation 2228
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851257157"
variation 2229
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:149052530"
variation 2230
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:41291464"
variation 2231
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851257680"
variation 2232
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1242957860"
variation 2233
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:527848892"
variation 2234
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851258036"
variation 2235
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:756057332"
variation 2236
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:780027867"
variation 2237
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851258594"
variation 2239
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413539150"
variation 2241
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:200288019"
variation 2242..2248
/gene="SEMA4G"
/replace="act"
/replace="actcact"
/db_xref="dbSNP:748396129"
variation 2242
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1327673019"
variation 2245
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1208690414"
variation 2246
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851259631"
variation 2247
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1274190195"
variation 2249
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133904692"
variation 2250
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1159862173"
variation 2253
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:138505815"
variation 2254
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:140405167"
variation 2258
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851260166"
variation 2259
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1473694674"
variation 2262
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:779055594"
variation 2263
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:531476226"
variation 2265
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1286873399"
variation 2267
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:778047878"
variation 2269
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:145555722"
variation 2270..2295
/gene="SEMA4G"
/replace="ag"
/replace="aggatctgcggtgcaactgcagacag"
/db_xref="dbSNP:1351574365"
variation 2270
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1472206434"
variation 2271
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:771404491"
variation 2272
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415680566"
variation 2273
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851262875"
variation 2274
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851263063"
variation 2276
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851263236"
variation 2278
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:777161655"
variation 2279
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:138067900"
variation 2280
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1282725183"
variation 2282
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1354773723"
variation 2283
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1411329720"
variation 2285
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851264505"
variation 2287
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1305609497"
variation 2288
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851264866"
variation 2292..2294
/gene="SEMA4G"
/replace="a"
/replace="aca"
/db_xref="dbSNP:1349407594"
variation 2293
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1228303776"
variation 2294
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851265432"
variation 2295
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1285314078"
variation 2301
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1358827837"
variation 2308
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1226997498"
variation 2311
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:375760083"
variation 2314
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1438587910"
variation 2316
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:774176474"
variation 2318
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1249714433"
variation 2319
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:761489347"
variation 2320
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1188499233"
variation 2322..2341
/gene="SEMA4G"
/replace="gatgagggtgatgatgaggg"
/replace="gatgagggtgatgatgagggtgatgatgaggg"
/db_xref="dbSNP:772358119"
variation 2324
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:767433560"
variation 2325..2328
/gene="SEMA4G"
/replace="g"
/replace="gagg"
/db_xref="dbSNP:1851267553"
variation 2327
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:773199318"
variation 2328
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:760515196"
variation 2329
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1359315768"
variation 2335
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:145330425"
variation 2337
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:753794838"
variation 2337
/gene="SEMA4G"
/replace="g"
/replace="gg"
/replace="gggg"
/db_xref="dbSNP:1851268481"
variation 2338
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133905431"
variation 2339..2350
/gene="SEMA4G"
/replace="gggggctggggg"
/replace="gggggctggggggctggggg"
/db_xref="dbSNP:1406962803"
variation 2339..2343
/gene="SEMA4G"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1411362753"
variation 2339..2340
/gene="SEMA4G"
/replace=""
/replace="aa"
/db_xref="dbSNP:1851269415"
variation 2339
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:755038247"
variation 2341
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1369335681"
variation 2342
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1414869947"
variation 2343
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851270194"
variation 2344..2355
/gene="SEMA4G"
/replace="ctgggggcctgg"
/replace="ctgggggcctgggggcctgg"
/db_xref="dbSNP:1475018399"
variation 2344
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1335400856"
variation 2345
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590000321"
variation 2347
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1342807731"
variation 2350
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:565974154"
variation 2351
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590000368"
variation 2353
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1283942354"
variation 2357
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:927913032"
variation 2358
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851271928"
variation 2359
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1230873584"
variation 2360
/gene="SEMA4G"
/replace=""
/replace="c"
/db_xref="dbSNP:1487389551"
variation 2360
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851272264"
variation 2361
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851272553"
variation 2362
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1272774402"
variation 2364
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:752924036"
variation 2365
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1201126917"
variation 2366
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851273137"
variation 2369
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:539199769"
variation 2371
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:889434035"
variation 2373
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851273660"
variation 2378
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1011010207"
variation 2381
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851273972"
variation 2387
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851274114"
variation 2390
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:200801941"
variation 2391..2392
/gene="SEMA4G"
/replace=""
/replace="gc"
/replace="gccc"
/replace="gcccc"
/replace="gccccc"
/replace="gcccccc"
/replace="gccccccc"
/db_xref="dbSNP:rs1851274585"
variation 2391
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851274273"
variation 2391
/gene="SEMA4G"
/replace="g"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1554885050"
variation 2392..2396
/gene="SEMA4G"
/replace=""
/replace="cccca"
/db_xref="dbSNP:1851275324"
variation 2392..2395
/gene="SEMA4G"
/replace="ccc"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1307646381"
variation 2392
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1564800318"
variation 2393..2400
/gene="SEMA4G"
/replace="ccc"
/replace="cccagccc"
/db_xref="dbSNP:1451113011"
variation 2393
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1490149544"
variation 2394
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1319007353"
variation 2396..2397
/gene="SEMA4G"
/replace=""
/replace="ag"
/db_xref="dbSNP:1244403035"
variation 2396
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:747411482"
variation 2397
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:757616280"
variation 2397
/gene="SEMA4G"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1851276615"
variation 2398..2413
/gene="SEMA4G"
/replace="ccccacc"
/replace="ccccaccacccccacc"
/db_xref="dbSNP:1851277127"
variation 2398..2401
/gene="SEMA4G"
/replace="cccc"
/replace="ccccccccccc"
/replace="ccccccccccccccc"
/db_xref="dbSNP:1564800345"
variation 2398
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1389197846"
variation 2399
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1434747606"
variation 2401..2406
/gene="SEMA4G"
/replace="c"
/replace="caccac"
/db_xref="dbSNP:1173800017"
variation 2401
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133906339"
variation 2402..2405
/gene="SEMA4G"
/replace=""
/replace="acca"
/db_xref="dbSNP:1399486489"
variation 2402
/gene="SEMA4G"
/replace=""
/replace="a"
/db_xref="dbSNP:1851277715"
variation 2402
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1326270062"
variation 2403
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:781570245"
variation 2404
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:746344453"
variation 2405
/gene="SEMA4G"
/replace=""
/replace="a"
/db_xref="dbSNP:1851278531"
variation 2405
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1438563345"
variation 2406..2425
/gene="SEMA4G"
/replace="cccccaccgcc"
/replace="cccccaccgcccccaccgcc"
/replace="cccccaccgcccccaccgcccccaccgcc"
/db_xref="dbSNP:773176617"
variation 2406..2410
/gene="SEMA4G"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:746736051"
variation 2407
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1334155427"
variation 2408
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:570600855"
variation 2411
/gene="SEMA4G"
/replace=""
/replace="a"
/db_xref="dbSNP:1366311394"
variation 2411
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1437736186"
variation 2412
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1465984153"
variation 2413
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:537981098"
variation 2414
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1364699879"
variation 2416
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1234288227"
variation 2418
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590000861"
variation 2420
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1257825267"
variation 2421
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1476929728"
variation 2422
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:773939741"
variation 2423
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1199749295"
variation 2426
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1268693928"
variation 2427
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:771918484"
variation 2428
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:772968534"
variation 2429
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:368791581"
variation 2430
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1454424276"
variation 2432
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133906812"
variation 2433
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1200638891"
variation 2435
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:766151814"
variation 2439
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:983229924"
variation 2440
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:776467523"
variation 2443
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:908616884"
variation 2444
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:759454826"
variation 2447
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:765317734"
variation 2448
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851283080"
variation 2449
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:941479176"
variation 2450
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:752836080"
variation 2451
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1318914837"
variation 2452
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1590001080"
variation 2459
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:764345648"
variation 2460
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851284021"
variation 2462
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1387547863"
variation 2465
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1303695342"
variation 2466
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:556496771"
variation 2467
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:757591403"
variation 2472
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:574711696"
variation 2473
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1331107517"
variation 2474
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851285121"
variation 2475
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1590001162"
variation 2476
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:781551217"
variation 2477
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1220506232"
variation 2478
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1590001187"
variation 2479
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1407498903"
variation 2483
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:746374262"
variation 2489
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851286122"
variation 2491
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:756701345"
variation 2492
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1211209380"
variation 2494
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851286938"
variation 2500
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:780702310"
variation 2501
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851287302"
variation 2506
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:747701115"
variation 2507
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:771687718"
variation 2510
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1413580384"
variation 2511
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:962140588"
variation 2512
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:976145243"
variation 2518
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:777592361"
variation 2519
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1157657574"
variation 2523
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1402208941"
variation 2525
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851288279"
variation 2526
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1411611036"
variation 2527
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1460684927"
variation 2529
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851288704"
variation 2530
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851288842"
variation 2533
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:921452117"
variation 2534
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851289124"
variation 2535
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1590001329"
variation 2540
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:376187099"
variation 2542
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1295465666"
variation 2546
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:776432076"
variation 2547
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1386472605"
variation 2549
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:141726768"
variation 2550
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:769758760"
variation 2553
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:554126222"
variation 2555
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851290572"
variation 2558
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851290768"
variation 2562
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:199549347"
variation 2563
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:764116745"
variation 2567
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:986379770"
variation 2571
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1246763144"
variation 2573
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1227060568"
variation 2576
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851291821"
variation 2577
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1177109703"
variation 2578
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1263267741"
variation 2584
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851292306"
variation 2585
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:751732798"
variation 2586
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1287154805"
variation 2587
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:150436471"
variation 2588
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:750866450"
variation 2589
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851292761"
variation 2594
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:756516259"
variation 2595
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:375024485"
variation 2597
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851293256"
variation 2598
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1250475715"
variation 2600
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1424709004"
variation 2601
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:754349112"
variation 2603
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851293867"
variation 2604
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1367130443"
variation 2605
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1424259786"
variation 2606
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:369095063"
variation 2607
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1372422706"
variation 2608
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1222819487"
variation 2610
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1590001608"
variation 2612
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:138231164"
variation 2614
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1052793166"
variation 2615
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1307300351"
variation 2616..2623
/gene="SEMA4G"
/replace="tctg"
/replace="tctgtctg"
/db_xref="dbSNP:1851296377"
variation 2618
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:149579572"
variation 2618
/gene="SEMA4G"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1056241246"
variation 2623
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851297087"
variation 2625
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1012519597"
variation 2626
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851297556"
variation 2628
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851297775"
variation 2629
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:770679319"
variation 2633
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851298209"
variation 2634..2635
/gene="SEMA4G"
/replace=""
/replace="g"
/db_xref="dbSNP:1851298451"
variation 2640
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:780708778"
variation 2641
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1011343221"
variation 2645
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:745721149"
variation 2646
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1276335802"
variation 2649
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:769527048"
variation 2650
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851299997"
variation 2654
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:879129411"
variation 2656
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1373716210"
variation 2657
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:775434918"
variation 2658
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:762807711"
variation 2664
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1483848011"
variation 2667
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:768734270"
variation 2674
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851301714"
variation 2677
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1173041083"
variation 2680
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:969880106"
variation 2681
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1003167771"
variation 2690
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1180250824"
variation 2692
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1257290025"
variation 2701
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851302969"
variation 2704..2706
/gene="SEMA4G"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1183256014"
variation 2706
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1482030451"
variation 2708..2710
/gene="SEMA4G"
/replace="ccc"
/replace="ccccc"
/db_xref="dbSNP:1256227888"
variation 2708
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133908720"
variation 2709
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1023540260"
variation 2716
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851304104"
variation 2719
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1436403588"
variation 2720
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:887726997"
variation 2722
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133908809"
variation 2723
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851304584"
variation 2724
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:781204292"
variation 2727
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851305040"
variation 2729
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1014839064"
variation 2732
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851305511"
variation 2733
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:962032640"
variation 2747
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:976114197"
variation 2749
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:745690393"
variation 2752
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851306652"
variation 2753
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851306867"
variation 2754
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851307077"
variation 2763
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851307315"
variation 2768
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:950718210"
variation 2770..2771
/gene="SEMA4G"
/replace=""
/replace="ag"
/db_xref="dbSNP:1590001957"
variation 2773..2798
/gene="SEMA4G"
/replace=""
/replace="caggcccagccaaagccccctcctca"
/db_xref="dbSNP:1590001967"
variation 2775
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851308106"
variation 2776
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851308337"
variation 2777
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:953557741"
variation 2778
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1362537886"
variation 2782
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:986736713"
variation 2786
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:982791219"
variation 2788..2792
/gene="SEMA4G"
/replace="ccccc"
/replace="cccccc"
/db_xref="dbSNP:1851309403"
variation 2789
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1410299026"
variation 2794
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:908564430"
variation 2797..2798
/gene="SEMA4G"
/replace=""
/replace="ca"
/db_xref="dbSNP:2133909252"
variation 2800
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:962745699"
variation 2801
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1453609825"
variation 2803
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:974131731"
variation 2804
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:921398275"
variation 2805
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851310611"
variation 2806
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1308719600"
variation 2810
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133909360"
variation 2813
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1564800882"
variation 2817
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851311037"
variation 2819
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1416775905"
variation 2821
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851311226"
variation 2822
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1193893340"
variation 2824
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:932827701"
variation 2827
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1385143611"
variation 2829
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:947584470"
variation 2831
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:977712151"
variation 2833
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1242406016"
variation 2834
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851312352"
variation 2835
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1333845024"
variation 2836
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:564705467"
variation 2837
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:912794871"
variation 2838
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1342470994"
variation 2840
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1331866472"
variation 2845
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851313372"
exon 2851..3977
/gene="SEMA4G"
/inference="alignment:Splign:2.1.0"
variation 2851
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1169802472"
variation 2854
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:2133910482"
variation 2856
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1358850075"
variation 2860
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:761133475"
variation 2861
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1191685942"
variation 2862
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851322719"
variation 2864
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:565832622"
variation 2865
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1301023166"
variation 2867
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1238599331"
variation 2868
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:140873008"
variation 2869..2872
/gene="SEMA4G"
/replace="atat"
/replace="atatat"
/db_xref="dbSNP:1180219371"
variation 2870
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:775161961"
variation 2871
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851323614"
variation 2873
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1435583593"
variation 2874
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1347264509"
variation 2880
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:755490675"
variation 2881
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1022174562"
variation 2882
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851324366"
variation 2884
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1282490941"
variation 2893
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1232746478"
variation 2895
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851325083"
variation 2901..2903
/gene="SEMA4G"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1564801111"
variation 2901
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1015510000"
variation 2904
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:551143626"
variation 2906
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1309192746"
variation 2907
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1446522565"
variation 2908
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851326399"
variation 2910
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1313501848"
variation 2912
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851326936"
variation 2913
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851327156"
variation 2915
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1381487456"
variation 2921
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1370845164"
variation 2930
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1212785459"
variation 2931
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:962694375"
variation 2932
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851328377"
variation 2935
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:11591349"
variation 2936
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:536866327"
variation 2937
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1250348904"
variation 2941
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1447859281"
variation 2942
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1186203566"
variation 2943
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:977649336"
variation 2946
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133911153"
variation 2950
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:756712868"
variation 2953
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1204147027"
variation 2954
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:556345883"
variation 2955
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1434047317"
variation 2957
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851330601"
variation 2959
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1173815254"
variation 2960
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:567995095"
variation 2961
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:986972740"
variation 2964
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1322261528"
variation 2970
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1386272160"
variation 2971
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1468467340"
variation 2972
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851331669"
variation 2973
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:745459702"
variation 2975
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:755937099"
variation 2976
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851332127"
variation 2979
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242453332"
variation 2980
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:11190780"
variation 2981
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1369013608"
variation 2985
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1217004954"
variation 2987
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:749061715"
variation 2995
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1323427412"
variation 2996
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:768679541"
variation 2997
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:562213978"
variation 3000
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1463832678"
variation 3001
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1215245125"
variation 3003
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1392099800"
variation 3006
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1247539943"
variation 3007
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851334603"
variation 3009
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1489476783"
variation 3010
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851335052"
variation 3015
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:774150942"
variation 3016
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1330576370"
variation 3017
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:554180516"
variation 3018
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1161357971"
variation 3019
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1222920929"
variation 3024..3028
/gene="SEMA4G"
/replace="ct"
/replace="cttct"
/db_xref="dbSNP:1409419478"
variation 3027..3031
/gene="SEMA4G"
/replace="ct"
/replace="ctcct"
/db_xref="dbSNP:1399901647"
variation 3032
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851337089"
variation 3033
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1164988814"
variation 3035
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1347204536"
variation 3038..3042
/gene="SEMA4G"
/replace="tt"
/replace="ttctt"
/db_xref="dbSNP:1851337943"
variation 3040
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1351283007"
variation 3042
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851338509"
variation 3048
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:748317224"
variation 3051
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1301958846"
variation 3055
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851339309"
variation 3060
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1350650732"
variation 3061
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:771987099"
variation 3062
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:909015462"
variation 3063
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:947024954"
variation 3065
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1348931588"
variation 3081
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1044109678"
variation 3082
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851341027"
variation 3090
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851341287"
variation 3094
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851341554"
variation 3096
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1223598937"
variation 3099
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:941896553"
variation 3105
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1590003340"
variation 3106..3109
/gene="SEMA4G"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:749161619"
variation 3106
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:867056759"
variation 3108
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851342959"
variation 3109
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1341846221"
variation 3113
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1323698735"
variation 3116
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1219725456"
variation 3117
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:897779980"
variation 3118
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1483432059"
variation 3120
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:766759551"
variation 3121
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133912160"
variation 3123
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1398820091"
variation 3126
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:938445182"
variation 3127
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1249568875"
variation 3129..3131
/gene="SEMA4G"
/replace="t"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:1564801421"
variation 3137
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851345504"
variation 3139
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851345730"
variation 3141
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133912278"
variation 3143..3145
/gene="SEMA4G"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:34661749"
variation 3143
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1469396700"
variation 3145
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1590003500"
variation 3148
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1051674712"
variation 3149
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1473643656"
variation 3150
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415748001"
variation 3156
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1403242646"
variation 3158
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851347694"
variation 3159
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851347910"
variation 3160
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413115744"
variation 3164
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1186071819"
variation 3165
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1162547813"
variation 3166
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1370560535"
variation 3172
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:889128459"
variation 3173
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851348837"
variation 3174
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1431132181"
variation 3179..3187
/gene="SEMA4G"
/replace="ctcc"
/replace="ctcccctcc"
/db_xref="dbSNP:1310336433"
variation 3181
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851349496"
variation 3182
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1056944101"
variation 3185
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851350086"
variation 3187
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:886274992"
variation 3189
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1828080527"
variation 3192..3198
/gene="SEMA4G"
/replace="cct"
/replace="ccttcct"
/db_xref="dbSNP:1442168150"
variation 3192
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1285150909"
variation 3193
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:150176473"
variation 3196
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1284040676"
variation 3201
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1243979563"
variation 3203
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1454985511"
variation 3207
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1016127185"
variation 3208
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1342914307"
variation 3209
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1207413139"
variation 3212
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1272637340"
variation 3214..3219
/gene="SEMA4G"
/replace=""
/replace="atcagc"
/db_xref="dbSNP:1437134295"
variation 3214
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:546548368"
variation 3217..3226
/gene="SEMA4G"
/replace=""
/replace="agcctcccca"
/db_xref="dbSNP:1232285107"
variation 3220
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851353656"
variation 3221
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851353903"
variation 3222..3225
/gene="SEMA4G"
/replace="ccc"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1851354331"
variation 3222
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:999055334"
variation 3223..3227
/gene="SEMA4G"
/replace="c"
/replace="cccac"
/db_xref="dbSNP:1188248769"
variation 3224
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:558511473"
variation 3226
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851355064"
variation 3227
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1471688492"
variation 3228..3229
/gene="SEMA4G"
/replace=""
/replace="gtgtga"
/db_xref="dbSNP:1279740182"
variation 3228
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564801584"
variation 3229
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1182551535"
variation 3235
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1390425592"
variation 3236
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:866465441"
variation 3238
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:899127927"
variation 3239
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851356441"
variation 3245..3246
/gene="SEMA4G"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1851356699"
variation 3250..3252
/gene="SEMA4G"
/replace="t"
/replace="tat"
/db_xref="dbSNP:776469814"
variation 3250
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:1564801613"
variation 3251
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:995448141"
variation 3252
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1406943937"
variation 3253..3258
/gene="SEMA4G"
/replace="gaga"
/replace="gagaga"
/db_xref="dbSNP:1031921038"
variation 3254
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1352660512"
variation 3255
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1166136937"
variation 3257
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:960318556"
variation 3261
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851358185"
variation 3266
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1217254719"
variation 3269
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:993082702"
variation 3270
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851358464"
variation 3271
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851358683"
variation 3273
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:576676078"
variation 3274
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851359112"
variation 3276
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:954125817"
variation 3277
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1409881469"
variation 3282
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1590004029"
variation 3283
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1335465291"
variation 3284
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1361197103"
variation 3286
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1450956457"
variation 3292
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1314573273"
variation 3293
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242083934"
variation 3295..3296
/gene="SEMA4G"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1366179476"
variation 3295
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851361189"
variation 3297
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1734059355"
variation 3298..3301
/gene="SEMA4G"
/replace="aaca"
/replace="aacaaca"
/db_xref="dbSNP:398114688"
variation 3299..3306
/gene="SEMA4G"
/replace="acac"
/replace="acacacac"
/db_xref="dbSNP:146737296"
variation 3299
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851362081"
variation 3301
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1470152414"
variation 3302
/gene="SEMA4G"
/replace=""
/replace="c"
/db_xref="dbSNP:1554885387"
variation 3304..3307
/gene="SEMA4G"
/replace="c"
/replace="cacc"
/db_xref="dbSNP:1564801730"
variation 3304
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:980911684"
variation 3312
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:908989869"
variation 3313
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1318120156"
variation 3316
/gene="SEMA4G"
/replace=""
/replace="a"
/db_xref="dbSNP:1851363694"
variation 3317
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1297128475"
variation 3318..3319
/gene="SEMA4G"
/replace=""
/replace="at"
/db_xref="dbSNP:201653131"
variation 3319
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851363979"
variation 3320
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:941859324"
variation 3322
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1275426272"
variation 3328
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:544003449"
variation 3335
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:561580399"
variation 3340
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:987306998"
variation 3341
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1761267634"
variation 3347
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851365080"
variation 3348
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:760046546"
variation 3351
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851365638"
variation 3359
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:570837619"
variation 3361
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851366097"
variation 3362
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1461145737"
variation 3363
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:956410819"
variation 3367
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1172757131"
variation 3368
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590004294"
variation 3372
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:765696472"
variation 3373..3380
/gene="SEMA4G"
/replace="ctgt"
/replace="ctgtctgt"
/db_xref="dbSNP:1851367609"
variation 3373
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851367435"
variation 3375
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:776736066"
variation 3387
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:541757083"
variation 3388
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1455911411"
variation 3390
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133914046"
variation 3392
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:947649741"
variation 3393
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:540658889"
variation 3398
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1458477096"
variation 3400
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851368804"
variation 3415
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:979738620"
variation 3416
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133914138"
variation 3417
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1419920691"
variation 3435
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851369510"
variation 3438
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:926970920"
variation 3440
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:938406307"
variation 3447
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1345587818"
variation 3452..3460
/gene="SEMA4G"
/replace="ggatg"
/replace="ggatggatg"
/db_xref="dbSNP:1156991738"
variation 3453
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1590004435"
variation 3458
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1411538590"
variation 3459
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1447292211"
variation 3460
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1057292576"
variation 3470
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1401448436"
variation 3471
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:148889377"
variation 3473
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1354019972"
variation 3476
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1357855929"
variation 3477
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:185501392"
variation 3478
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1437149072"
variation 3479
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1393859490"
variation 3482
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1314077837"
variation 3486..3487
/gene="SEMA4G"
/replace="c"
/replace="cc"
/db_xref="dbSNP:745620184"
variation 3492
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851373532"
variation 3493
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1357883329"
variation 3495
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1058101"
variation 3496..3500
/gene="SEMA4G"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1564801889"
variation 3497
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1043523463"
variation 3499
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1440759734"
variation 3500
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1037520890"
variation 3501
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851374834"
variation 3507
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851375125"
variation 3511
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851375359"
variation 3516..3520
/gene="SEMA4G"
/replace="tc"
/replace="tcctc"
/db_xref="dbSNP:1851375586"
variation 3517
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1287105200"
variation 3518
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:899075093"
variation 3520
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851376270"
variation 3521
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:758453345"
variation 3522
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:999022475"
variation 3524
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:533032857"
variation 3526
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851377123"
variation 3531
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851377286"
variation 3533..3541
/gene="SEMA4G"
/replace="gggaaaggg"
/replace="gggaaagggggaaaggg"
/db_xref="dbSNP:1237569905"
variation 3533
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1276666015"
variation 3539
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851377980"
variation 3540..3546
/gene="SEMA4G"
/replace="ggag"
/replace="ggaggag"
/db_xref="dbSNP:1212458091"
variation 3546
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:539958411"
variation 3552
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1031806643"
variation 3554
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:996061169"
variation 3555..3559
/gene="SEMA4G"
/replace="tgtct"
/replace="tgtctgtct"
/db_xref="dbSNP:1851379088"
variation 3555..3557
/gene="SEMA4G"
/replace="t"
/replace="tgt"
/db_xref="dbSNP:1851378916"
variation 3556
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1276056518"
variation 3557
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1318520975"
variation 3560
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851379758"
variation 3563
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1028300853"
variation 3564
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1222315298"
variation 3569
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:145456828"
variation 3571
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851380461"
variation 3575
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1259577119"
variation 3576
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851380817"
variation 3577
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851380992"
variation 3583
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:969446661"
variation 3587
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851381422"
variation 3591
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1313689869"
variation 3592
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851381840"
variation 3595
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851382067"
variation 3601
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:980495734"
variation 3603
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1016423976"
variation 3605
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851382772"
variation 3609
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:764283941"
variation 3610
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851383229"
variation 3611
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851383454"
variation 3612
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:889784981"
variation 3613
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851383892"
variation 3618
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851384118"
variation 3619
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1482005638"
variation 3620
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1008277694"
variation 3621
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:751801892"
variation 3627
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133915301"
variation 3632
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1590004825"
variation 3635
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851385217"
variation 3636..3637
/gene="SEMA4G"
/replace=""
/replace="ct"
/db_xref="dbSNP:971792769"
variation 3636
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851385462"
variation 3637
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:919060865"
variation 3639
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851386135"
variation 3648
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:1851386346"
variation 3649
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1365943648"
variation 3650
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1160574437"
variation 3651
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:549901293"
variation 3652
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851387327"
variation 3653
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:987778470"
variation 3655
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:956145941"
variation 3659
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1189614913"
variation 3660
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1484440106"
variation 3664
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851388353"
variation 3665
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851388576"
variation 3666
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:722435"
variation 3668
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851389219"
variation 3669
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:2133915599"
variation 3671
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1174615834"
variation 3673
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1377821148"
variation 3674
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1486785377"
variation 3676
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851390176"
variation 3678
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851390425"
variation 3679
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1021817552"
variation 3683
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851390914"
variation 3687
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1258766345"
variation 3688
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:13114"
variation 3690
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:530575708"
variation 3697
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1322070191"
variation 3698
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851392002"
variation 3700
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851392246"
variation 3702
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590005004"
variation 3704
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851392702"
variation 3708
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1294208197"
variation 3711
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851393161"
variation 3716
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:796584525"
variation 3717
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851393640"
variation 3720
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1443718900"
variation 3721
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:549209014"
variation 3722..3726
/gene="SEMA4G"
/replace="ccccc"
/replace="cccccc"
/db_xref="dbSNP:1851394245"
variation 3724
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851394479"
variation 3726
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1851394644"
variation 3727
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1272765213"
variation 3728
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:535391514"
variation 3731
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:2133915982"
variation 3735
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:722434"
variation 3736
/gene="SEMA4G"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:756150215"
variation 3737
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851395747"
variation 3739..3747
/gene="SEMA4G"
/replace="tga"
/replace="tgaggatga"
/db_xref="dbSNP:1851395903"
variation 3742
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1287595742"
variation 3744
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1590005102"
variation 3745..3750
/gene="SEMA4G"
/replace="tg"
/replace="tgactg"
/db_xref="dbSNP:1282127784"
variation 3749..3751
/gene="SEMA4G"
/replace="t"
/replace="tgt"
/db_xref="dbSNP:1851396880"
variation 3750
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851397104"
variation 3753
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851397297"
variation 3754
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851397538"
variation 3759
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1851397765"
variation 3763
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1453577215"
variation 3764
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851398062"
variation 3765
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1339982424"
variation 3770
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:992545494"
variation 3771
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1473984676"
variation 3775
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:377579383"
variation 3778
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1193217573"
variation 3782
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1429752865"
variation 3783
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:535979784"
variation 3785
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851399630"
variation 3786
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1053207362"
variation 3793
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1204475752"
variation 3798
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1468760178"
variation 3801
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851400265"
variation 3802
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:895968520"
variation 3809
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:547453410"
variation 3810
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1215821939"
variation 3813
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1014460178"
variation 3815
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851401422"
variation 3818
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1272754894"
variation 3822
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590005244"
variation 3825
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:566052365"
variation 3826
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:1228291159"
variation 3827
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:539856889"
variation 3828..3835
/gene="SEMA4G"
/replace="aatg"
/replace="aatgaatg"
/db_xref="dbSNP:1851402794"
variation 3831
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1294126122"
variation 3834
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:1245235656"
variation 3835
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1023629686"
variation 3844
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:907599520"
variation 3845
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851403820"
variation 3846
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1194666457"
variation 3848
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1459569804"
variation 3851
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851404319"
variation 3854
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1397200065"
variation 3857
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1006217092"
variation 3859
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851405001"
variation 3863
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:940472396"
variation 3867
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1370830712"
variation 3868
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851405676"
variation 3871
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851405873"
variation 3873
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851406098"
variation 3876
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564802346"
variation 3879
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1168572915"
variation 3883
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1454629864"
variation 3887
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851406807"
variation 3893
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1015896546"
variation 3894
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1183846917"
variation 3895
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1590005486"
variation 3896..3897
/gene="SEMA4G"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1851407769"
variation 3896
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1037468969"
variation 3897
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1267016453"
variation 3898
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851408064"
variation 3900
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:971763006"
variation 3901
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:780109310"
variation 3911
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851408894"
variation 3914
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:920446283"
variation 3916
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1590005630"
variation 3917..3922
/gene="SEMA4G"
/replace="ggggag"
/replace="ggggagggggag"
/db_xref="dbSNP:1851409933"
variation 3917
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1026045787"
variation 3918
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1249625499"
variation 3922
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1397803701"
variation 3923
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851410880"
variation 3925
/gene="SEMA4G"
/replace="a"
/replace="t"
/db_xref="dbSNP:11190781"
variation 3926
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:1851411332"
variation 3928
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:375892284"
variation 3935
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590005760"
variation 3937
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851412105"
variation 3938
/gene="SEMA4G"
/replace=""
/replace="t"
/db_xref="dbSNP:1348958879"
variation 3938
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590005788"
variation 3941
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1441105677"
variation 3942
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:890411724"
variation 3943
/gene="SEMA4G"
/replace="a"
/replace="c"
/db_xref="dbSNP:2133917246"
variation 3944
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1008640180"
variation 3945
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:576811967"
variation 3946..3947
/gene="SEMA4G"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1851413621"
variation 3947
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:537243928"
variation 3948
/gene="SEMA4G"
/replace="a"
/replace="g"
/db_xref="dbSNP:555966416"
variation 3949
/gene="SEMA4G"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:573637014"
variation 3951
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:934667679"
variation 3952
/gene="SEMA4G"
/replace="g"
/replace="t"
/db_xref="dbSNP:1171676783"
regulatory 3955..3960
/regulatory_class="polyA_signal_sequence"
/gene="SEMA4G"
/note="hexamer: AATAAA"
variation 3963
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:866768376"
variation 3964
/gene="SEMA4G"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1010346124"
variation 3965
/gene="SEMA4G"
/replace="c"
/replace="g"
/db_xref="dbSNP:1851414998"
variation 3966
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851415299"
variation 3970
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:917372450"
variation 3971..3974
/gene="SEMA4G"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1439739794"
variation 3972
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1590006249"
variation 3974
/gene="SEMA4G"
/replace="c"
/replace="t"
/db_xref="dbSNP:1851416502"
polyA_site 3977
/gene="SEMA4G"
/note="major polyA site"
ORIGIN
agccgcggccccttcctctcgcagctggtgctgtggggccgcggagccgcgcgtcgctgtctctatggccccggatccgagcgcaaagtctgggcctccccaggaagatgtgggggaggctctggcccctcctcctcagcatcctcacagcaactgcagtcccaggaccctcactgcggagaccgtctagagaactagatgccacccctcggatgaccataccctatgaagagctctctgggacccggcacttcaagggccaagcccagaactactcaacactgctgctggaggaggcctcagcaaggctgctggtgggagcccgaggtgccctgttctctctcagtgccaacgacataggagatggggctcacaaagagatccactgggaagcctccccagagatgcaaagcaaatgtcatcaaaaagggaaaaacaaccagacggagtgctttaaccatgtgcggttcctgcagcggctcaattctacccacctctatgcatgtgggactcacgccttccagcccctctgtgcagccattgatgctgaggccttcaccttgccaaccagcttcgaggaggggaaggagaagtgtccttatgacccagcccgtggcttcacaggcctcatcattgatggaggcctctacacagccactaggtatgaattccggagcattcctgacatccgccggagccgccacccacactccctgagaactgaggagacaccaatgcattggctcaatgatgcggagtttgtgttctccgtcctcgtgcgggagagcaaggccagtgcagtgggtgatgatgacaaggtgtactacttcttcacggagcgtgccactgaggagggctctggcagcttcactcagagccgcagcagtcaccgtgtggcccgtgtggctcgtgtctgcaagggagacctgggagggaagaagatcctgcagaagaagtggacttccttcctgaaagcccgtctcatctgccacattccactgtatgagacactgcgtggggtctgcagcctggatgctgaaacctcaagccgtacacacttctatgcagccttcacgctgagcacacagtggaagaccctggaggcctcagccatctgccgctatgacctggcagagatccaggctgtctttgcaggaccctatatggaataccaggatggttcccggcgctggggtcgctatgagggtggggtgcctgagccccggcctggctcgtgtatcacagattcattgcgcagccaaggctacaattcatcccaagacttgccatccctggtcctggactttgtaaagttgcacccactgatggctcggcccgttgtgcccacacgtggacggcccctgctgctcaagcgcaacatacgctacacacaccttacagggacacctgtcaccacgcctgctggacctacctatgacctgctctttctgggcacagctgatggctggatccacaaggccgtagtcctgggctctgggatgcacattattgaagagacacaagtgttcagggagtcccagtctgtggaaaatctagtcatctctctattgcagcacagcctctatgtgggggctcctagcggagtcatccagctaccactctccagctgctcccgctaccgatcctgctatgactgcatcttggcccgagacccctactgtggctgggaccctggcacccatgcctgcgcagcagccaccaccatagccaacaggacagcactgatacaggacatagagagaggaaatcgaggctgtgagagcagcagggatacagggccaccaccaccactgaagacccgctctgtgctccggggtgatgatgtcctcctgccctgtgaccagccatccaacctggcccgggccttgtggctactcaatgggagcatgggcctgagcgatgggcagggtggctaccgtgtgggcgtggacgggctgctggttacagatgcacagcctgagcacagtggcaactatggctgctatgccgaggaaaatggcctccgcaccctgctggcctcctatagtctcacagtccggccagccactcctgccccagctccaaaagcccctgccacacctggggcacagctggcacctgatgtgagactgctctatgtgctagccattgccgcgcttggtggcctctgcctcatcctggcctcctccctcctctatgtggcctgtctgcgggaaggcagacgagggcgccgacggaaatactcactgggtcgggccagccgggcaggaggatctgcggtgcaactgcagacagtctcaggccagtgtcctggagaggaagatgagggtgatgatgagggggctgggggcctggagggcagctgtctccagatcatccctggggagggagccccagccccaccacccccaccgcccccaccgccaccggctgagctgaccaatggcttggtggcactgcccagccggctgcggaggatgaatggcaatagctatgtgcttctgaggcagagcaacaatggagtaccagcagggccctgctccttcgccgaggaactcagccgcatcctggaaaaaaggaagcacacgcagctcgtggagcagctagatgagagctctgtctgagcccagcctcccagaacaaatgctcttccaagccagcctatctgtcccaggctgggccactgcctccctaacacagccaccctcccttcattacccccactccatacccttctcccaactttttgatgtccctgtagggctggccagtcaggcccagccaaagccccctcctcagtctccacagacccacatgtgagcagcccaggcccatcggtgctcctcagaggcagggctctgcaggtccatatgggctcaatgtcaccaccctctgcatggccctgtgtgctggatggtcctgaaaccagacaagacctctgccagccacctaagccctgcgtacattcacatgcacacatggaagaatgtttatcggctgggctgcagtgcccccaccctcaccttctcctggtgcattcttgtttcatccctgcttctggacttggggtaccctcccaattgccacatcctatctggtcctcttccccagccccatgtggtgacctctttgtcaagagcttgggaacgggccagcctggggaggtaagactgcatcactcccctcctctcccttcctgtgtggcccttgtgaatcagcctccccactctccttggtcattctcaagagtatgagagacagagctccaggcatgtcccatccccatgcacatgtggtaacacacacctgtatcacacatgtgcttacatttccactcacatgcacctctgagcctcccttgctgtcttggacctgtctgttgggtttagtccgtggacatttcagagggagatccccctcccatttaactgtcctcacaggcccttgcctaggatggatgaccaacactgcactcaatgagccagcctctcttttgggggaatcaagcatttgcttcctctagactacagcagggaaagggaggagaaatctgatgtctcaactggcacatgaagcccattcttggaactatgcaaagggcagaggctgggagtttggacgcttagctcctacccctgtcctacctcaccggggcactttcaggggccaggggcctctgaagtctctaggcctatatgggacaatcaattctgactgagctcccccattcccctcgggtgaggatgactgttatttttgtagctgagaacgtggaatcccacgggtttttactgcccttcacccaacctctcccacctccaccccacaatgaatgtatttattgtgagaatggctacacttctttaggaatgcccccacttacaaccaggtgggtggaacaggcatgtgacagagtggggagcctgggctcagctcctccccctgccgttggttaataaacaccctttttccccaca
//
by
@meso_cacase at
DBCLS
This page is licensed under a
Creative Commons Attribution 4.0 International License (CC BY 4.0).
If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596.
[Full Text]