Primary Site >> Liver Cancer

Gene >> SLC27A3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000368661
Start 153775450:153775450(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.94T>C
AA Mutation p.Phe32Leu(p.F32L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000368661
Start 153777793:153777793(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1210G>C
AA Mutation p.Ala404Pro(p.A404P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000368661
Start 153778320:153778320(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772719483
CDS Mutation c.1462C>T
AA Mutation p.Arg488Trp(p.R488W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence frameshift_variant
Transcription ID ENST00000368661
Start 153775947:153775948(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.591_592insT
AA Mutation p.Gly198TrpfsTer105(p.G198Wfs*105)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 5
Mutation Consequence inframe_deletion
Transcription ID ENST00000368661
Start 153777780:153777797(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1197_1214delATCCAAGTTCTCGGCTGG
AA Mutation p.Lys399_Gly405delinsAsn(p.K399_G405delinsN)
Mutation Classification In_Frame_Del
Feature Type Transcript
ID 6
Mutation Consequence inframe_deletion
Transcription ID ENST00000368661
Start 153775391:153775393(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.37_39delGAG
AA Mutation p.Glu13del(p.E13del)
Mutation Classification In_Frame_Del
Feature Type Transcript