Primary Site >> Stomach Cancer

Gene >> DAPK2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261891
Start 63983745:63983745(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.102T>G
AA Mutation p.Phe34Leu(p.F34L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261891
Start 63983702:63983702(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.145T>C
AA Mutation p.Tyr49His(p.Y49H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000261891
Start 63930443:63930443(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.596T>C
AA Mutation p.Val199Ala(p.V199A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000261891
Start 63911954:63911954(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.986C>G
AA Mutation p.Thr329Ser(p.T329S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000261891
Start 64040187:64040187(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377251760
CDS Mutation c.75C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000261891
Start 63908568:63908568(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1065C>T
Mutation Classification Silent
Feature Type Transcript