Primary Site >> Stomach Cancer

Gene >> DHH

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000266991
Start 49091197:49091197(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750409317
CDS Mutation c.496G>A
AA Mutation p.Ala166Thr(p.A166T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000266991
Start 49094325:49094325(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.188C>T
AA Mutation p.Ala63Val(p.A63V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000266991
Start 49091154:49091154(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.539A>G
AA Mutation p.Asn180Ser(p.N180S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000266991
Start 49094339:49094339(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.174C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000266991
Start 49091288:49091288(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748745609
CDS Mutation c.405C>T
Mutation Classification Silent
Feature Type Transcript