Primary Site >> Liver Cancer

Gene >> TF

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000402696
Start 133768145:133768145(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752715864
CDS Mutation c.1603G>A
AA Mutation p.Gly535Ser(p.G535S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000402696
Start 133757869:133757869(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.971T>C
AA Mutation p.Val324Ala(p.V324A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence frameshift_variant
Transcription ID ENST00000402696
Start 133775485:133775486(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1740_1741delGC
AA Mutation p.Leu580PhefsTer4(p.L580Ffs*4)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 4
Mutation Consequence frameshift_variant
Transcription ID ENST00000402696
Start 133757867:133757868(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.970dupG
AA Mutation p.Val324GlyfsTer14(p.V324Gfs*14)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000402696
Start 133755467:133755468(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.609dupA
AA Mutation p.Tyr204IlefsTer28(p.Y204Ifs*28)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 6
Mutation Consequence splice_donor_variant;coding_sequence_variant
Transcription ID ENST00000402696
Start 133764253:133764276(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1276_1297+2delGTCTTGGCAGAAAACTACAATAGT
Mutation Classification Splice_Site
Feature Type Transcript