Primary Site >> Stomach Cancer

Gene >> ETNK1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000266517
Start 22643899:22643899(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.560G>A
AA Mutation p.Arg187Gln(p.R187Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000266517
Start 22643971:22643971(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.632T>C
AA Mutation p.Ile211Thr(p.I211T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000266517
Start 22673560:22673560(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749131482
CDS Mutation c.1112G>A
AA Mutation p.Arg371His(p.R371H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000266517
Start 22643882:22643882(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.543G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000266517
Start 22673534:22673534(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1086T>C
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence stop_gained;inframe_insertion
Transcription ID ENST00000266517
Start 22643848:22643849(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.509_510insTTGATCCCCTGTCCC
AA Mutation p.Gly170_Asn171insTer(p.G170_N171ins*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000266517
Start 22643850:22643851(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.512_513insATGTCCA
AA Mutation p.Asn171LysfsTer4(p.N171Kfs*4)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript