Primary Site >> Esophagus Cancer

Gene >> SCN8A

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000354534
Start 51806584:51806584(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5098C>G
AA Mutation p.Gln1700Glu(p.Q1700E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000354534
Start 51765934:51765934(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2808G>C
AA Mutation p.Glu936Asp(p.E936D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000354534
Start 51705456:51705456(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752265946
CDS Mutation c.1174G>A
AA Mutation p.Val392Ile(p.V392I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000354534
Start 51769098:51769098(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs550579591
CDS Mutation c.3135C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000354534
Start 51762640:51762640(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772945312
CDS Mutation c.2508C>T
Mutation Classification Silent
Feature Type Transcript