Primary Site >> Stomach Cancer

Gene >> HELT

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000515777
Start 185020390:185020390(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762115587
CDS Mutation c.347C>T
AA Mutation p.Ala116Val(p.A116V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000515777
Start 185020705:185020705(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.662A>G
AA Mutation p.Asn221Ser(p.N221S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000515777
Start 185020713:185020713(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.670G>A
AA Mutation p.Gly224Ser(p.G224S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000515777
Start 185019485:185019485(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.126G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000515777
Start 185019806:185019806(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.192A>G
Mutation Classification Silent
Feature Type Transcript