Primary Site >> Stomach Cancer

Gene >> ADH5

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000296412
Start 99082061:99082061(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.170C>T
AA Mutation p.Pro57Leu(p.P57L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000296412
Start 99072436:99072436(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773778500
CDS Mutation c.1106G>A
AA Mutation p.Arg369Gln(p.R369Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000296412
Start 99081977:99081977(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779698938
CDS Mutation c.254C>T
AA Mutation p.Ala85Val(p.A85V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000296412
Start 99074970:99074970(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.905C>T
AA Mutation p.Ala302Val(p.A302V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000296412
Start 99076445:99076445(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.672C>T
Mutation Classification Silent
Feature Type Transcript