Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FAT3

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92354168:92354168(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1606A>G
AA Mutation p.Thr536Ala(p.T536A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92354255:92354255(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1693T>G
AA Mutation p.Phe565Val(p.F565V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92798241:92798241(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4778C>T
AA Mutation p.Ala1593Val(p.A1593V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92798948:92798948(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778886701
CDS Mutation c.5485G>A
AA Mutation p.Gly1829Ser(p.G1829S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92354957:92354957(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2395C>T
AA Mutation p.Leu799Phe(p.L799F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92798310:92798310(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4847C>T
AA Mutation p.Ala1616Val(p.A1616V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92843965:92843965(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10148C>T
AA Mutation p.Ser3383Phe(p.S3383F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92798915:92798915(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5452G>A
AA Mutation p.Val1818Ile(p.V1818I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92774058:92774058(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199959583
CDS Mutation c.3763G>A
AA Mutation p.Ala1255Thr(p.A1255T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92866903:92866903(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11371C>T
AA Mutation p.Arg3791Cys(p.R3791C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92352884:92352884(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs538781318
CDS Mutation c.322C>T
AA Mutation p.Arg108Cys(p.R108C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92524775:92524775(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2984C>T
AA Mutation p.Ala995Val(p.A995V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92867022:92867022(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11490C>G
AA Mutation p.Ser3830Arg(p.S3830R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92801591:92801591(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765949446
CDS Mutation c.8128G>A
AA Mutation p.Glu2710Lys(p.E2710K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92352784:92352784(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765974517
CDS Mutation c.222G>T
AA Mutation p.Lys74Asn(p.K74N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92353511:92353511(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.949G>T
AA Mutation p.Asp317Tyr(p.D317Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92835002:92835002(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9554A>G
AA Mutation p.Asn3185Ser(p.N3185S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92798987:92798987(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5524T>A
AA Mutation p.Ser1842Thr(p.S1842T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92831960:92831960(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9370C>T
AA Mutation p.Leu3124Phe(p.L3124F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92844292:92844292(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10475A>G
AA Mutation p.His3492Arg(p.H3492R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92353502:92353502(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.940G>T
AA Mutation p.Asp314Tyr(p.D314Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92354645:92354645(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2083G>T
AA Mutation p.Gly695Cys(p.G695C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92890943:92890943(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373934891
CDS Mutation c.13150G>A
AA Mutation p.Val4384Met(p.V4384M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92882929:92882929(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.12023T>C
AA Mutation p.Ile4008Thr(p.I4008T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92353410:92353410(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200065507
CDS Mutation c.848G>A
AA Mutation p.Arg283Gln(p.R283Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92354216:92354216(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1654G>T
AA Mutation p.Ala552Ser(p.A552S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92857249:92857249(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10951G>A
AA Mutation p.Glu3651Lys(p.E3651K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92524808:92524808(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3017T>C
AA Mutation p.Val1006Ala(p.V1006A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92840704:92840704(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs537765652
CDS Mutation c.10061G>A
AA Mutation p.Arg3354Gln(p.R3354Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92835041:92835041(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376234071
CDS Mutation c.9593C>T
AA Mutation p.Ala3198Val(p.A3198V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92867086:92867086(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11554C>T
AA Mutation p.Arg3852Cys(p.R3852C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92798487:92798487(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756801253
CDS Mutation c.5024C>T
AA Mutation p.Thr1675Met(p.T1675M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92890965:92890965(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.13172C>A
AA Mutation p.Ser4391Tyr(p.S4391Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92353296:92353296(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.734T>A
AA Mutation p.Val245Asp(p.V245D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92799677:92799677(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6214A>T
AA Mutation p.Ile2072Phe(p.I2072F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 36
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92800401:92800401(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6938C>T
AA Mutation p.Pro2313Leu(p.P2313L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 37
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92761916:92761916(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3280G>C
AA Mutation p.Val1094Leu(p.V1094L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 38
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92789977:92789977(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3920G>A
AA Mutation p.Gly1307Asp(p.G1307D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 39
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92844718:92844718(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs202061798
CDS Mutation c.10901G>A
AA Mutation p.Arg3634His(p.R3634H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 40
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92790171:92790171(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748097452
CDS Mutation c.4114G>A
AA Mutation p.Glu1372Lys(p.E1372K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 41
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92352885:92352885(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780559377
CDS Mutation c.323G>A
AA Mutation p.Arg108His(p.R108H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 42
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92792878:92792878(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4273G>T
AA Mutation p.Val1425Leu(p.V1425L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 43
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92831669:92831669(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9079G>T
AA Mutation p.Val3027Phe(p.V3027F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 44
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92799199:92799199(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5736T>A
AA Mutation p.His1912Gln(p.H1912Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 45
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92799935:92799935(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6472C>A
AA Mutation p.Gln2158Lys(p.Q2158K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 46
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92857256:92857256(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369650040
CDS Mutation c.10958C>T
AA Mutation p.Pro3653Leu(p.P3653L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 47
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92352957:92352957(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.395A>G
AA Mutation p.Tyr132Cys(p.Y132C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 48
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92883102:92883102(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.12196G>A
AA Mutation p.Gly4066Arg(p.G4066R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 49
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92843982:92843982(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs531488417
CDS Mutation c.10165G>A
AA Mutation p.Val3389Met(p.V3389M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 50
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92867072:92867072(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11540C>T
AA Mutation p.Pro3847Leu(p.P3847L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 51
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92882833:92882833(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11927C>T
AA Mutation p.Pro3976Leu(p.P3976L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 52
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92891003:92891003(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200062618
CDS Mutation c.13210G>A
AA Mutation p.Gly4404Ser(p.G4404S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 53
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92882890:92882890(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11984C>T
AA Mutation p.Ala3995Val(p.A3995V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 54
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92798662:92798662(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5199T>G
AA Mutation p.Phe1733Leu(p.F1733L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 55
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92352915:92352915(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.353T>C
AA Mutation p.Val118Ala(p.V118A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 56
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92882946:92882946(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765324804
CDS Mutation c.12040G>A
AA Mutation p.Val4014Ile(p.V4014I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 57
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92801282:92801282(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374977464
CDS Mutation c.7819G>A
AA Mutation p.Val2607Ile(p.V2607I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 58
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92882983:92882983(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.12077G>A
AA Mutation p.Arg4026His(p.R4026H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 59
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92353382:92353382(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760614096
CDS Mutation c.820C>T
AA Mutation p.Pro274Ser(p.P274S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 60
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92883012:92883012(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.12106C>T
AA Mutation p.Arg4036Cys(p.R4036C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 61
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92353386:92353386(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776497356
CDS Mutation c.824G>A
AA Mutation p.Arg275Gln(p.R275Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 62
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92353981:92353981(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1419C>A
AA Mutation p.Phe473Leu(p.F473L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 63
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92524830:92524830(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3039G>T
AA Mutation p.Lys1013Asn(p.K1013N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 64
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92798899:92798899(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5436C>A
AA Mutation p.Phe1812Leu(p.F1812L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 65
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000525166
Start 92889889:92889889(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747818054
CDS Mutation c.12695G>A
AA Mutation p.Arg4232Gln(p.R4232Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 66
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92890678:92890678(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.12885C>A
AA Mutation p.Phe4295Leu(p.F4295L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 67
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92800740:92800740(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7277A>G
AA Mutation p.Asp2426Gly(p.D2426G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 68
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92801675:92801675(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8212A>G
AA Mutation p.Thr2738Ala(p.T2738A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 69
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92883382:92883382(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.12476C>T
AA Mutation p.Ala4159Val(p.A4159V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 70
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92883381:92883381(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.12475G>A
AA Mutation p.Ala4159Thr(p.A4159T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 71
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92355213:92355213(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2651T>C
AA Mutation p.Val884Ala(p.V884A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 72
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92798058:92798058(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4595A>C
AA Mutation p.Glu1532Ala(p.E1532A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 73
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92889196:92889196(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.12609A>G
AA Mutation p.Ile4203Met(p.I4203M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 74
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92762019:92762019(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3383C>T
AA Mutation p.Ala1128Val(p.A1128V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 75
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92798315:92798315(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4852G>A
AA Mutation p.Val1618Ile(p.V1618I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 76
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92798432:92798432(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs566312497
CDS Mutation c.4969C>T
AA Mutation p.Arg1657Trp(p.R1657W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 77
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92353629:92353629(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1067A>G
AA Mutation p.Tyr356Cys(p.Y356C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 78
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92354253:92354253(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1691A>G
AA Mutation p.Asp564Gly(p.D564G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 79
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92790135:92790135(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377563244
CDS Mutation c.4078C>T
AA Mutation p.Arg1360Trp(p.R1360W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 80
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92844142:92844142(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10325A>G
AA Mutation p.Gln3442Arg(p.Q3442R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 81
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92859305:92859305(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11191C>T
AA Mutation p.Pro3731Ser(p.P3731S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 82
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92792956:92792956(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4351C>G
AA Mutation p.Leu1451Val(p.L1451V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 83
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92798210:92798210(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374615122
CDS Mutation c.4747C>T
AA Mutation p.Arg1583Cys(p.R1583C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 84
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92355156:92355156(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2594A>G
AA Mutation p.Lys865Arg(p.K865R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 85
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92798332:92798332(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4869A>T
AA Mutation p.Gln1623His(p.Q1623H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 86
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92798697:92798697(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5234C>A
AA Mutation p.Pro1745His(p.P1745H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 87
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92882783:92882783(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11877C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 88
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92352922:92352922(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.360T>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 89
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92891005:92891005(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.13212C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 90
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92866929:92866929(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11397G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 91
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92790170:92790170(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4113C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 92
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92797972:92797972(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4509T>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 93
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92798092:92798092(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4629C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 94
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92836697:92836697(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9768G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 95
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92801227:92801227(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7764C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 96
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92524734:92524734(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2943C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 97
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92866809:92866809(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11277C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 98
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92355346:92355346(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2784C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 99
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92882807:92882807(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11901C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 100
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92355160:92355160(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2598G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 101
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92831866:92831866(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9276G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 102
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92844653:92844653(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10836C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 103
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92524713:92524713(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376947953
CDS Mutation c.2922C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 104
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92353828:92353828(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs72970548
CDS Mutation c.1266C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 105
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92801788:92801788(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769303051
CDS Mutation c.8325G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 106
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92797861:92797861(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4398C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 107
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92800972:92800972(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7509C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 108
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92831977:92831977(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs114152693
CDS Mutation c.9387C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 109
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92353705:92353705(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1143T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 110
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92801122:92801122(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7659G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 111
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92352994:92352994(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200428460
CDS Mutation c.432G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 112
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92799839:92799839(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6376C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 113
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92857227:92857227(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779979255
CDS Mutation c.10929G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 114
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92801875:92801875(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs192587610
CDS Mutation c.8412C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 115
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92353555:92353555(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.993G>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 116
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92880828:92880828(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11775C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 117
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92882831:92882831(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11925G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 118
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92800972:92800972(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7509C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 119
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92798425:92798425(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4962C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 120
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92831941:92831941(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9351A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 121
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92354779:92354779(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370314147
CDS Mutation c.2217C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 122
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92837800:92837800(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9912G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 123
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92831665:92831665(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9075T>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 124
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92890579:92890579(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.12786G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 125
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92890615:92890615(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759657516
CDS Mutation c.12822C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 126
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92799874:92799874(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760100485
CDS Mutation c.6411C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 127
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92801476:92801476(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8013C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 128
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92800669:92800669(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7206C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 129
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92844350:92844350(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771480729
CDS Mutation c.10533C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 130
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92353726:92353726(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1164C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 131
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92801104:92801104(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765879241
CDS Mutation c.7641C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 132
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92800267:92800267(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6804C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 133
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92800936:92800936(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376936376
CDS Mutation c.7473C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 134
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92844032:92844032(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10215A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 135
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92866956:92866956(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11424C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 136
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92524780:92524780(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758628483
CDS Mutation c.2989C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 137
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92354386:92354386(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs570286992
CDS Mutation c.1824T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 138
Mutation Consequence frameshift_variant
Transcription ID ENST00000525166
Start 92799110:92799110(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.5650delG
AA Mutation p.Val1884SerfsTer21(p.V1884Sfs*21)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 139
Mutation Consequence frameshift_variant
Transcription ID ENST00000525166
Start 92354101:92354101(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1542delC
AA Mutation p.Met515CysfsTer42(p.M515Cfs*42)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 140
Mutation Consequence frameshift_variant
Transcription ID ENST00000525166
Start 92355013:92355013(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2456delG
AA Mutation p.Gly819ValfsTer17(p.G819Vfs*17)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 141
Mutation Consequence frameshift_variant
Transcription ID ENST00000525166
Start 92524923:92524923(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.3138delT
AA Mutation p.Phe1046LeufsTer9(p.F1046Lfs*9)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 142
Mutation Consequence frameshift_variant
Transcription ID ENST00000525166
Start 92883135:92883135(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.12233delC
AA Mutation p.Pro4078ArgfsTer36(p.P4078Rfs*36)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 143
Mutation Consequence stop_gained
Transcription ID ENST00000525166
Start 92697416:92697416(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3190C>T
AA Mutation p.Arg1064Ter(p.R1064*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 144
Mutation Consequence stop_gained
Transcription ID ENST00000525166
Start 92859260:92859260(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11146C>T
AA Mutation p.Arg3716Ter(p.R3716*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 145
Mutation Consequence stop_gained
Transcription ID ENST00000525166
Start 92354431:92354431(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1869C>A
AA Mutation p.Cys623Ter(p.C623*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 146
Mutation Consequence frameshift_variant
Transcription ID ENST00000525166
Start 92798835:92798836(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.5378dupA
AA Mutation p.Asn1793LysfsTer14(p.N1793Kfs*14)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 147
Mutation Consequence frameshift_variant
Transcription ID ENST00000525166
Start 92883145:92883146(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.12243dupC
AA Mutation p.Val4082ArgfsTer13(p.V4082Rfs*13)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 148
Mutation Consequence frameshift_variant
Transcription ID ENST00000525166
Start 92524922:92524923(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.3138dupT
AA Mutation p.Ala1047CysfsTer51(p.A1047Cfs*51)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 149
Mutation Consequence frameshift_variant
Transcription ID ENST00000525166
Start 92889212:92889213(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.12627dupT
AA Mutation p.Val4210CysfsTer6(p.V4210Cfs*6)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> FAT3

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92859209:92859209(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11095C>T
AA Mutation p.Arg3699Trp(p.R3699W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92353658:92353658(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1096T>A
AA Mutation p.Leu366Met(p.L366M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92798903:92798903(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5440A>G
AA Mutation p.Ser1814Gly(p.S1814G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92866894:92866894(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11362G>A
AA Mutation p.Val3788Met(p.V3788M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92762018:92762018(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3382G>T
AA Mutation p.Ala1128Ser(p.A1128S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92762019:92762019(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3383C>T
AA Mutation p.Ala1128Val(p.A1128V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92799036:92799036(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5573G>T
AA Mutation p.Gly1858Val(p.G1858V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92883051:92883051(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201053443
CDS Mutation c.12145G>A
AA Mutation p.Ala4049Thr(p.A4049T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92801537:92801537(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8074G>A
AA Mutation p.Asp2692Asn(p.D2692N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92764985:92764985(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3641A>C
AA Mutation p.Glu1214Ala(p.E1214A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92799033:92799033(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5570T>A
AA Mutation p.Val1857Asp(p.V1857D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92801784:92801784(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8321T>G
AA Mutation p.Phe2774Cys(p.F2774C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92801045:92801045(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7582G>A
AA Mutation p.Val2528Ile(p.V2528I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92832003:92832003(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9413C>A
AA Mutation p.Pro3138His(p.P3138H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92800517:92800517(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757504785
CDS Mutation c.7054G>A
AA Mutation p.Val2352Ile(p.V2352I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92837676:92837676(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9788C>T
AA Mutation p.Ser3263Phe(p.S3263F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92353236:92353236(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.674G>T
AA Mutation p.Arg225Ile(p.R225I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92353965:92353965(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1403G>A
AA Mutation p.Gly468Glu(p.G468E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92774125:92774125(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751543920
CDS Mutation c.3830C>T
AA Mutation p.Ser1277Phe(p.S1277F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92799453:92799453(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5990C>T
AA Mutation p.Ser1997Phe(p.S1997F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92890678:92890678(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.12885C>A
AA Mutation p.Phe4295Leu(p.F4295L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92799657:92799657(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6194G>C
AA Mutation p.Gly2065Ala(p.G2065A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92798345:92798345(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4882C>G
AA Mutation p.Leu1628Val(p.L1628V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92800752:92800752(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7289G>T
AA Mutation p.Arg2430Ile(p.R2430I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92859261:92859261(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11147G>A
AA Mutation p.Arg3716Gln(p.R3716Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000525166
Start 92790136:92790136(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768777673
CDS Mutation c.4079G>A
AA Mutation p.Arg1360Gln(p.R1360Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92867097:92867097(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11565C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92353369:92353369(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.807C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92764980:92764980(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780359938
CDS Mutation c.3636C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000525166
Start 92790041:92790041(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3984G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence stop_gained
Transcription ID ENST00000525166
Start 92801585:92801585(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8122C>T
AA Mutation p.Gln2708Ter(p.Q2708*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence stop_gained
Transcription ID ENST00000525166
Start 92353811:92353811(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1249C>T
AA Mutation p.Arg417Ter(p.R417*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence stop_gained
Transcription ID ENST00000525166
Start 92797895:92797895(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4432G>T
AA Mutation p.Glu1478Ter(p.E1478*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript