Primary Site >> Liver Cancer

Gene >> NR2F2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000394166
Start 96332508:96332508(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.403C>A
AA Mutation p.Arg135Ser(p.R135S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000394166
Start 96334403:96334403(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.770C>G
AA Mutation p.Ala257Gly(p.A257G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence stop_gained;frameshift_variant
Transcription ID ENST00000394166
Start 96332378:96332379(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.273_274delCG
AA Mutation p.Tyr91Ter(p.Y91*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence inframe_deletion
Transcription ID ENST00000394166
Start 96334284:96334307(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.652_675delAGGATGCTCTTCAGCGCCGTCGAG
AA Mutation p.Arg218_Glu225del(p.R218_E225del)
Mutation Classification In_Frame_Del
Feature Type Transcript