Primary Site >> Esophagus Cancer

Gene >> RFC1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000381897
Start 39304852:39304852(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2075A>T
AA Mutation p.Glu692Val(p.E692V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000381897
Start 39327591:39327591(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.497T>C
AA Mutation p.Leu166Pro(p.L166P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000381897
Start 39295673:39295673(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2898C>A
AA Mutation p.His966Gln(p.H966Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000381897
Start 39308766:39308766(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1755C>T
Mutation Classification Silent
Feature Type Transcript