Primary Site >> Stomach Cancer

Gene >> DOK1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000233668
Start 74556519:74556519(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.851G>A
AA Mutation p.Gly284Asp(p.G284D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000233668
Start 74556777:74556777(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751060609
CDS Mutation c.1109C>A
AA Mutation p.Pro370Gln(p.P370Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000233668
Start 74556337:74556337(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.669C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence frameshift_variant
Transcription ID ENST00000233668
Start 74554783:74554783(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.35delT
AA Mutation p.Leu12CysfsTer26(p.L12Cfs*26)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000233668
Start 74554782:74554783(version: GRCh38)
Mutation Type INS
dbSNP_RS rs759252474
CDS Mutation c.35dupT
AA Mutation p.Leu12PhefsTer33(p.L12Ffs*33)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000233668
Start 74556339:74556340(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.675dupC
AA Mutation p.Ser226LeufsTer15(p.S226Lfs*15)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript