Primary Site >> Stomach Cancer

Gene >> ANK2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113356842:113356842(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8224C>T
AA Mutation p.His2742Tyr(p.H2742Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113330332:113330332(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2987G>T
AA Mutation p.Arg996Leu(p.R996L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113356282:113356282(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7664C>T
AA Mutation p.Thr2555Ile(p.T2555I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113282844:113282844(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2051A>G
AA Mutation p.Lys684Arg(p.K684R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113373415:113373415(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs542400709
CDS Mutation c.11825G>A
AA Mutation p.Arg3942His(p.R3942H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113345904:113345904(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770698838
CDS Mutation c.4253G>A
AA Mutation p.Arg1418His(p.R1418H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000357077
Start 113333056:113333056(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3227C>A
AA Mutation p.Pro1076His(p.P1076H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113278512:113278512(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1835C>T
AA Mutation p.Ala612Val(p.A612V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113373160:113373160(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11681C>T
AA Mutation p.Thr3894Ile(p.T3894I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113353654:113353654(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5036G>C
AA Mutation p.Gly1679Ala(p.G1679A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113353925:113353925(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5307A>T
AA Mutation p.Lys1769Asn(p.K1769N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113350231:113350231(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs564648496
CDS Mutation c.4408G>A
AA Mutation p.Asp1470Asn(p.D1470N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113355652:113355652(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7034A>G
AA Mutation p.Glu2345Gly(p.E2345G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113356219:113356219(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7601G>T
AA Mutation p.Ser2534Ile(p.S2534I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113358960:113358960(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10342A>G
AA Mutation p.Ser3448Gly(p.S3448G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113373099:113373099(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11620A>G
AA Mutation p.Met3874Val(p.M3874V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113356954:113356954(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8336C>T
AA Mutation p.Ala2779Val(p.A2779V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113333083:113333083(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759670378
CDS Mutation c.3254C>T
AA Mutation p.Ala1085Val(p.A1085V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113356179:113356179(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776531245
CDS Mutation c.7561A>G
AA Mutation p.Ser2521Gly(p.S2521G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113354839:113354839(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6221G>T
AA Mutation p.Gly2074Val(p.G2074V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113330377:113330377(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3032G>A
AA Mutation p.Arg1011His(p.R1011H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113343053:113343053(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751096182
CDS Mutation c.4159G>A
AA Mutation p.Gly1387Ser(p.G1387S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113356883:113356883(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8265A>C
AA Mutation p.Glu2755Asp(p.E2755D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113353302:113353302(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4684G>T
AA Mutation p.Val1562Leu(p.V1562L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113355934:113355934(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7316C>T
AA Mutation p.Ala2439Val(p.A2439V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113240503:113240503(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.712C>A
AA Mutation p.His238Asn(p.H238N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113358357:113358357(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9739T>C
AA Mutation p.Ser3247Pro(p.S3247P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113381464:113381464(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11867A>T
AA Mutation p.Asn3956Ile(p.N3956I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113369720:113369720(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770954138
CDS Mutation c.11525G>A
AA Mutation p.Arg3842Gln(p.R3842Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 30
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000357077
Start 113237172:113237172(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.669G>T
AA Mutation p.Lys223Asn(p.K223N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113333092:113333092(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3263G>A
AA Mutation p.Arg1088Gln(p.R1088Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113373306:113373306(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs121912706
CDS Mutation c.11716C>T
AA Mutation p.Arg3906Trp(p.R3906W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113369675:113369675(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11480A>G
AA Mutation p.Gln3827Arg(p.Q3827R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113354590:113354590(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5972G>T
AA Mutation p.Arg1991Leu(p.R1991L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113356315:113356315(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7697A>G
AA Mutation p.His2566Arg(p.H2566R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 36
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113255762:113255762(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1018G>T
AA Mutation p.Ala340Ser(p.A340S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 37
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113277895:113277895(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1742T>G
AA Mutation p.Leu581Arg(p.L581R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 38
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113357538:113357538(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8920G>A
AA Mutation p.Ala2974Thr(p.A2974T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 39
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113357798:113357798(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9180A>C
AA Mutation p.Lys3060Asn(p.K3060N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 40
Mutation Consequence missense_variant
Transcription ID ENST00000357077
Start 113365081:113365081(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.10931A>G
AA Mutation p.Asp3644Gly(p.D3644G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000357077
Start 113356757:113356757(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs564510599
CDS Mutation c.8139C>T
Mutation Classification Silent
Feature Type Transcript
ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000357077
Start 113237082:113237082(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.579G>T
Mutation Classification Silent
Feature Type Transcript
ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000357077
Start 113345926:113345926(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776983267
CDS Mutation c.4275C>T
Mutation Classification Silent
Feature Type Transcript
ID 44
Mutation Consequence synonymous_variant
Transcription ID ENST00000357077
Start 113336768:113336768(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3783A>G
Mutation Classification Silent
Feature Type Transcript
ID 45
Mutation Consequence synonymous_variant
Transcription ID ENST00000357077
Start 113354396:113354396(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754030532
CDS Mutation c.5778G>A
Mutation Classification Silent
Feature Type Transcript
ID 46
Mutation Consequence synonymous_variant
Transcription ID ENST00000357077
Start 113330438:113330438(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767037865
CDS Mutation c.3093C>T
Mutation Classification Silent
Feature Type Transcript
ID 47
Mutation Consequence synonymous_variant
Transcription ID ENST00000357077
Start 113354162:113354162(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5544A>C
Mutation Classification Silent
Feature Type Transcript
ID 48
Mutation Consequence synonymous_variant
Transcription ID ENST00000357077
Start 113355749:113355749(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs553324580
CDS Mutation c.7131C>T
Mutation Classification Silent
Feature Type Transcript
ID 49
Mutation Consequence synonymous_variant
Transcription ID ENST00000357077
Start 113357147:113357147(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8529C>T
Mutation Classification Silent
Feature Type Transcript
ID 50
Mutation Consequence synonymous_variant
Transcription ID ENST00000357077
Start 113356931:113356931(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8313C>T
Mutation Classification Silent
Feature Type Transcript
ID 51
Mutation Consequence synonymous_variant
Transcription ID ENST00000357077
Start 113367594:113367594(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.11061C>T
Mutation Classification Silent
Feature Type Transcript
ID 52
Mutation Consequence synonymous_variant
Transcription ID ENST00000357077
Start 113240556:113240556(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.765G>A
Mutation Classification Silent
Feature Type Transcript
ID 53
Mutation Consequence synonymous_variant
Transcription ID ENST00000357077
Start 113292472:113292472(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779535881
CDS Mutation c.2334C>T
Mutation Classification Silent
Feature Type Transcript
ID 54
Mutation Consequence synonymous_variant
Transcription ID ENST00000357077
Start 113345905:113345905(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778974823
CDS Mutation c.4254C>T
Mutation Classification Silent
Feature Type Transcript
ID 55
Mutation Consequence synonymous_variant
Transcription ID ENST00000357077
Start 113357501:113357501(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8883T>C
Mutation Classification Silent
Feature Type Transcript
ID 56
Mutation Consequence synonymous_variant
Transcription ID ENST00000357077
Start 113354270:113354270(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5652G>A
Mutation Classification Silent
Feature Type Transcript
ID 57
Mutation Consequence synonymous_variant
Transcription ID ENST00000357077
Start 113237163:113237163(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148143699
CDS Mutation c.660A>G
Mutation Classification Silent
Feature Type Transcript
ID 58
Mutation Consequence synonymous_variant
Transcription ID ENST00000357077
Start 113274571:113274571(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1605C>T
Mutation Classification Silent
Feature Type Transcript
ID 59
Mutation Consequence synonymous_variant
Transcription ID ENST00000357077
Start 113343082:113343082(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4188C>T
Mutation Classification Silent
Feature Type Transcript
ID 60
Mutation Consequence frameshift_variant
Transcription ID ENST00000357077
Start 113356058:113356125(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.7440_7507delTGGAATTTTTCCAAGTCACTTTCCTCTTCCTGCAGCTGTTGCCAAAACAGAACTCTTGACGGAAGTGG
AA Mutation p.Gly2481LeufsTer11(p.G2481Lfs*11)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 61
Mutation Consequence frameshift_variant
Transcription ID ENST00000357077
Start 113357074:113357074(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.8460delA
AA Mutation p.Asp2821ThrfsTer41(p.D2821Tfs*41)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 62
Mutation Consequence frameshift_variant
Transcription ID ENST00000357077
Start 113373387:113373387(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.11800delG
AA Mutation p.Asp3934MetfsTer7(p.D3934Mfs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 63
Mutation Consequence frameshift_variant
Transcription ID ENST00000357077
Start 113369801:113369801(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.11609delA
AA Mutation p.Lys3870ArgfsTer27(p.K3870Rfs*27)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 64
Mutation Consequence frameshift_variant
Transcription ID ENST00000357077
Start 113353803:113353803(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.5190delA
AA Mutation p.Gly1731ValfsTer7(p.G1731Vfs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 65
Mutation Consequence frameshift_variant
Transcription ID ENST00000357077
Start 113343100:113343100(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.4212delT
AA Mutation p.Phe1404LeufsTer28(p.F1404Lfs*28)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 66
Mutation Consequence frameshift_variant
Transcription ID ENST00000357077
Start 113049797:113049797(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.73delA
AA Mutation p.Arg25AspfsTer27(p.R25Dfs*27)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 67
Mutation Consequence stop_gained
Transcription ID ENST00000357077
Start 113302836:113302836(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2545G>T
AA Mutation p.Glu849Ter(p.E849*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 68
Mutation Consequence stop_gained
Transcription ID ENST00000357077
Start 113363385:113363385(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10804C>T
AA Mutation p.Arg3602Ter(p.R3602*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 69
Mutation Consequence stop_gained
Transcription ID ENST00000357077
Start 113353680:113353680(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5062C>T
AA Mutation p.Gln1688Ter(p.Q1688*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 70
Mutation Consequence stop_gained
Transcription ID ENST00000357077
Start 113356638:113356638(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8020A>T
AA Mutation p.Lys2674Ter(p.K2674*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript