Primary Site >> Liver Cancer

Gene >> HCFC2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000229330
Start 104086888:104086888(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1105A>G
AA Mutation p.Thr369Ala(p.T369A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000229330
Start 104082840:104082840(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1002T>C
Mutation Classification Silent
Feature Type Transcript
ID 3
Mutation Consequence frameshift_variant
Transcription ID ENST00000229330
Start 104080825:104080826(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.763_764delAA
AA Mutation p.Asn255GlnfsTer12(p.N255Qfs*12)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 4
Mutation Consequence frameshift_variant
Transcription ID ENST00000229330
Start 104080803:104080803(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.741delT
AA Mutation p.His248IlefsTer6(p.H248Ifs*6)
Mutation Classification Frame_Shift_Del
Feature Type Transcript