Primary Site >> Esophagus Cancer

Gene >> VCP

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000358901
Start 35062279:35062279(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.883A>G
AA Mutation p.Lys295Glu(p.K295E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000358901
Start 35067912:35067912(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.281T>C
AA Mutation p.Val94Ala(p.V94A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000358901
Start 35060390:35060390(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765061140
CDS Mutation c.1618A>G
AA Mutation p.Ile540Val(p.I540V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000358901
Start 35067941:35067941(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.252G>A
AA Mutation p.Met84Ile(p.M84I)
Mutation Classification Missense_Mutation
Feature Type Transcript