Primary Site >> Liver Cancer

Gene >> MLXIPL

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000313375
Start 73605732:73605732(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.857T>G
AA Mutation p.Leu286Arg(p.L286R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000313375
Start 73605960:73605960(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.770T>C
AA Mutation p.Phe257Ser(p.F257S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000313375
Start 73599665:73599665(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs146487355
CDS Mutation c.932C>T
AA Mutation p.Pro311Leu(p.P311L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000313375
Start 73594294:73594294(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2420C>G
AA Mutation p.Ser807Cys(p.S807C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000313375
Start 73624224:73624224(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.269T>C
AA Mutation p.Phe90Ser(p.F90S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000313375
Start 73605967:73605967(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.763A>G
AA Mutation p.Thr255Ala(p.T255A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000313375
Start 73595661:73595661(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2286G>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000313375
Start 73597188:73597189(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1557_1596dupCACTGCGGGGAGCAACAACCCCTGCCTCACACAGCTGCTC
AA Mutation p.Thr533HisfsTer17(p.T533Hfs*17)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 9
Mutation Consequence inframe_deletion;splice_region_variant
Transcription ID ENST00000313375
Start 73605749:73605766(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.823_840delTACGTCGGCAATGCTGAC
AA Mutation p.Tyr275_Asp280del(p.Y275_D280del)
Mutation Classification In_Frame_Del
Feature Type Transcript