Primary Site >> Stomach Cancer

Gene >> YES1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000314574
Start 732942:732942(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1315A>G
AA Mutation p.Thr439Ala(p.T439A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000314574
Start 736939:736939(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1160T>G
AA Mutation p.Ile387Ser(p.I387S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000314574
Start 747955:747955(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.435T>C
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000314574
Start 736827:736827(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1272T>C
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000314574
Start 732849:732849(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779772570
CDS Mutation c.1408C>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence stop_gained
Transcription ID ENST00000314574
Start 745763:745763(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.669T>A
AA Mutation p.Tyr223Ter(p.Y223*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript