Primary Site >> Esophagus Cancer

Gene >> CDC20

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000310955
Start 43360573:43360573(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.828G>C
AA Mutation p.Trp276Cys(p.W276C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence splice_donor_variant
Transcription ID ENST00000310955
Start 43360098:43360099(version: GRCh38)
Mutation Type INS
dbSNP_RS rs755204301
CDS Mutation c.556+2dupT
Mutation Classification Splice_Site
Feature Type Transcript