Primary Site >> Stomach Cancer

Gene >> HDAC10

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000216271
Start 50248053:50248053(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1174G>T
AA Mutation p.Ala392Ser(p.A392S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000216271
Start 50248251:50248251(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1055C>A
AA Mutation p.Pro352Gln(p.P352Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000216271
Start 50245713:50245713(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1948C>A
AA Mutation p.Leu650Met(p.L650M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000216271
Start 50248137:50248137(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs541010302
CDS Mutation c.1090G>A
AA Mutation p.Ala364Thr(p.A364T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000216271
Start 50247777:50247777(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1338-1G>T
Mutation Classification Splice_Site
Feature Type Transcript