Primary Site >> Esophagus Cancer

Gene >> PCGF2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000611883
Start 38736137:38736137(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.610G>A
AA Mutation p.Glu204Lys(p.E204K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000611883
Start 38736138:38736138(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.609G>T
AA Mutation p.Lys203Asn(p.K203N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000611883
Start 38735526:38735526(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.732C>G
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence frameshift_variant
Transcription ID ENST00000611883
Start 38736105:38736105(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.642delC
AA Mutation p.Tyr215ThrfsTer24(p.Y215Tfs*24)
Mutation Classification Frame_Shift_Del
Feature Type Transcript