Primary Site >> Stomach Cancer

Gene >> RBFOX1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000547338
Start 7709120:7709120(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138704494
CDS Mutation c.1060G>A
AA Mutation p.Val354Ile(p.V354I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000547338
Start 7518264:7518264(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755458164
CDS Mutation c.145G>A
AA Mutation p.Ala49Thr(p.A49T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000547338
Start 7664946:7664946(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.908G>A
AA Mutation p.Gly303Glu(p.G303E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000547338
Start 7518331:7518331(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.212C>T
AA Mutation p.Thr71Met(p.T71M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000547338
Start 7518165:7518165(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779321097
CDS Mutation c.46G>A
AA Mutation p.Ala16Thr(p.A16T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000547338
Start 7587257:7587257(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.425A>C
AA Mutation p.Lys142Thr(p.K142T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000547338
Start 7653892:7653892(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766300841
CDS Mutation c.835G>A
AA Mutation p.Val279Met(p.V279M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000547338
Start 7518388:7518388(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.269C>G
AA Mutation p.Thr90Arg(p.T90R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000547338
Start 7595630:7595630(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.550C>T
AA Mutation p.Arg184Cys(p.R184C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000547338
Start 7630606:7630606(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145006582
CDS Mutation c.680C>T
AA Mutation p.Thr227Met(p.T227M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000547338
Start 7595561:7595561(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.481G>A
AA Mutation p.Val161Ile(p.V161I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000547338
Start 7710724:7710724(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1173C>T
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000547338
Start 7709062:7709062(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1002A>G
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000547338
Start 7595560:7595560(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.480C>T
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000547338
Start 7630637:7630637(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.711A>G
Mutation Classification Silent
Feature Type Transcript
ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000547338
Start 7597400:7597403(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.594_597delTAAA
AA Mutation p.Asn198LysfsTer13(p.N198Kfs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 17
Mutation Consequence frameshift_variant
Transcription ID ENST00000547338
Start 7710729:7710730(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1182dupT
AA Mutation p.Ala395CysfsTer35(p.A395Cfs*35)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript