Primary Site >> Stomach Cancer

Gene >> CELSR3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48660990:48660990(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1645C>T
AA Mutation p.Arg549Cys(p.R549C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48645487:48645487(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7753G>A
AA Mutation p.Ala2585Thr(p.A2585T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48659411:48659411(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3224G>T
AA Mutation p.Arg1075Leu(p.R1075L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48659922:48659922(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755186680
CDS Mutation c.2713C>T
AA Mutation p.Arg905Cys(p.R905C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48640053:48640053(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758292109
CDS Mutation c.9532C>T
AA Mutation p.Arg3178Trp(p.R3178W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48662031:48662031(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754864877
CDS Mutation c.604G>A
AA Mutation p.Ala202Thr(p.A202T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48660851:48660851(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1784T>C
AA Mutation p.Ile595Thr(p.I595T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48660734:48660734(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1901C>T
AA Mutation p.Thr634Met(p.T634M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48656709:48656709(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4388C>T
AA Mutation p.Pro1463Leu(p.P1463L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48649184:48649184(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6504G>T
AA Mutation p.Gln2168His(p.Q2168H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48662204:48662204(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.431G>A
AA Mutation p.Arg144Gln(p.R144Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48659448:48659448(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3187A>G
AA Mutation p.Asn1063Asp(p.N1063D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48661524:48661524(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1111C>T
AA Mutation p.Arg371Cys(p.R371C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48661847:48661847(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.788G>A
AA Mutation p.Arg263His(p.R263H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48657160:48657160(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3937T>G
AA Mutation p.Phe1313Val(p.F1313V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48660134:48660134(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2501C>A
AA Mutation p.Ser834Tyr(p.S834Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48661754:48661754(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.881G>A
AA Mutation p.Arg294His(p.R294H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48659564:48659564(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375268987
CDS Mutation c.3071G>A
AA Mutation p.Arg1024Gln(p.R1024Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48661328:48661328(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1307C>T
AA Mutation p.Ala436Val(p.A436V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48659960:48659960(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771709882
CDS Mutation c.2675G>A
AA Mutation p.Arg892His(p.R892H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48661290:48661290(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1345G>T
AA Mutation p.Gly449Cys(p.G449C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48640424:48640424(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9161G>T
AA Mutation p.Gly3054Val(p.G3054V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48659181:48659181(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754395490
CDS Mutation c.3454C>T
AA Mutation p.Arg1152Trp(p.R1152W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48661458:48661458(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1177C>T
AA Mutation p.Arg393Cys(p.R393C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48659825:48659825(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2810G>A
AA Mutation p.Gly937Asp(p.G937D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48662321:48662321(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.314C>T
AA Mutation p.Pro105Leu(p.P105L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48653052:48653052(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748113150
CDS Mutation c.5584C>T
AA Mutation p.Arg1862Trp(p.R1862W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48662030:48662030(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.605C>T
AA Mutation p.Ala202Val(p.A202V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48653898:48653898(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5258G>A
AA Mutation p.Gly1753Asp(p.G1753D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48651448:48651448(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6097G>A
AA Mutation p.Gly2033Arg(p.G2033R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48659054:48659054(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758290257
CDS Mutation c.3581G>A
AA Mutation p.Arg1194His(p.R1194H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48647948:48647948(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs574354699
CDS Mutation c.7022G>A
AA Mutation p.Arg2341His(p.R2341H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48653099:48653099(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5537G>A
AA Mutation p.Gly1846Asp(p.G1846D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48659130:48659130(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3505C>T
AA Mutation p.Leu1169Phe(p.L1169F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48657049:48657049(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4048G>A
AA Mutation p.Glu1350Lys(p.E1350K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 36
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48654403:48654403(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5038C>T
AA Mutation p.Pro1680Ser(p.P1680S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 37
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48659499:48659499(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3136C>A
AA Mutation p.Pro1046Thr(p.P1046T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 38
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48655101:48655101(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4931G>A
AA Mutation p.Gly1644Asp(p.G1644D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 39
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48661889:48661889(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.746C>A
AA Mutation p.Pro249Gln(p.P249Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 40
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48660080:48660080(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2555A>G
AA Mutation p.Asn852Ser(p.N852S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 41
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48662292:48662292(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.343G>A
AA Mutation p.Val115Ile(p.V115I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 42
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48662486:48662486(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.149C>T
AA Mutation p.Thr50Met(p.T50M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 43
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48659135:48659135(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3500C>A
AA Mutation p.Pro1167His(p.P1167H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 44
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48661044:48661044(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1591G>A
AA Mutation p.Val531Ile(p.V531I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 45
Mutation Consequence missense_variant
Transcription ID ENST00000164024
Start 48652475:48652475(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5713G>A
AA Mutation p.Ala1905Thr(p.A1905T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 46
Mutation Consequence synonymous_variant
Transcription ID ENST00000164024
Start 48659746:48659746(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2889C>A
Mutation Classification Silent
Feature Type Transcript
ID 47
Mutation Consequence synonymous_variant
Transcription ID ENST00000164024
Start 48646173:48646173(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7380G>A
Mutation Classification Silent
Feature Type Transcript
ID 48
Mutation Consequence synonymous_variant
Transcription ID ENST00000164024
Start 48662065:48662065(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.570C>T
Mutation Classification Silent
Feature Type Transcript
ID 49
Mutation Consequence synonymous_variant
Transcription ID ENST00000164024
Start 48659167:48659167(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3468C>T
Mutation Classification Silent
Feature Type Transcript
ID 50
Mutation Consequence synonymous_variant
Transcription ID ENST00000164024
Start 48660478:48660478(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2157G>A
Mutation Classification Silent
Feature Type Transcript
ID 51
Mutation Consequence synonymous_variant
Transcription ID ENST00000164024
Start 48648393:48648393(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6846G>A
Mutation Classification Silent
Feature Type Transcript
ID 52
Mutation Consequence synonymous_variant
Transcription ID ENST00000164024
Start 48660313:48660313(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779113277
CDS Mutation c.2322T>C
Mutation Classification Silent
Feature Type Transcript
ID 53
Mutation Consequence synonymous_variant
Transcription ID ENST00000164024
Start 48662158:48662158(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.477C>A
Mutation Classification Silent
Feature Type Transcript
ID 54
Mutation Consequence synonymous_variant
Transcription ID ENST00000164024
Start 48662209:48662209(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.426C>T
Mutation Classification Silent
Feature Type Transcript
ID 55
Mutation Consequence synonymous_variant
Transcription ID ENST00000164024
Start 48653778:48653778(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5289T>C
Mutation Classification Silent
Feature Type Transcript
ID 56
Mutation Consequence synonymous_variant
Transcription ID ENST00000164024
Start 48657146:48657146(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3951C>T
Mutation Classification Silent
Feature Type Transcript
ID 57
Mutation Consequence synonymous_variant
Transcription ID ENST00000164024
Start 48641520:48641520(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8829G>T
Mutation Classification Silent
Feature Type Transcript
ID 58
Mutation Consequence frameshift_variant
Transcription ID ENST00000164024
Start 48646874:48646874(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.7184delC
AA Mutation p.Pro2395HisfsTer22(p.P2395Hfs*22)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 59
Mutation Consequence frameshift_variant
Transcription ID ENST00000164024
Start 48652482:48652482(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.5706delC
AA Mutation p.Gly1903AlafsTer36(p.G1903Afs*36)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 60
Mutation Consequence frameshift_variant
Transcription ID ENST00000164024
Start 48661748:48661748(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.887delC
AA Mutation p.Pro296ArgfsTer12(p.P296Rfs*12)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 61
Mutation Consequence frameshift_variant
Transcription ID ENST00000164024
Start 48641480:48641480(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.8869delG
AA Mutation p.Glu2957SerfsTer36(p.E2957Sfs*36)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 62
Mutation Consequence frameshift_variant
Transcription ID ENST00000164024
Start 48661944:48661944(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.691delC
AA Mutation p.Arg231GlyfsTer77(p.R231Gfs*77)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 63
Mutation Consequence frameshift_variant
Transcription ID ENST00000164024
Start 48651998:48651998(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.5802delC
AA Mutation p.Ser1935AlafsTer4(p.S1935Afs*4)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 64
Mutation Consequence frameshift_variant
Transcription ID ENST00000164024
Start 48662482:48662482(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.153delG
AA Mutation p.Pro52GlnfsTer10(p.P52Qfs*10)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 65
Mutation Consequence stop_gained
Transcription ID ENST00000164024
Start 48659229:48659229(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3406C>T
AA Mutation p.Gln1136Ter(p.Q1136*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 66
Mutation Consequence frameshift_variant
Transcription ID ENST00000164024
Start 48660952:48660953(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1682dupA
AA Mutation p.His561GlnfsTer11(p.H561Qfs*11)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 67
Mutation Consequence frameshift_variant
Transcription ID ENST00000164024
Start 48655115:48655116(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.4913_4916dupCCGT
AA Mutation p.Ala1640ArgfsTer8(p.A1640Rfs*8)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 68
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000164024
Start 48646259:48646259(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7296-2A>G
Mutation Classification Splice_Site
Feature Type Transcript
ID 69
Mutation Consequence inframe_deletion
Transcription ID ENST00000164024
Start 48662108:48662110(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.525_527delTTT
AA Mutation p.Phe175del(p.F175del)
Mutation Classification In_Frame_Del
Feature Type Transcript