Primary Site >> Liver Cancer

Gene >> CUX1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000292535
Start 102196802:102196802(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs569218052
CDS Mutation c.1391C>A
AA Mutation p.Ser464Tyr(p.S464Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000292535
Start 102201611:102201611(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2314G>C
AA Mutation p.Glu772Gln(p.E772Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000292535
Start 102234225:102234225(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3607C>T
AA Mutation p.Arg1203Trp(p.R1203W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000292535
Start 102202190:102202190(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782375328
CDS Mutation c.2893A>G
AA Mutation p.Ile965Val(p.I965V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000292535
Start 102028117:102028117(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.161C>T
AA Mutation p.Ala54Val(p.A54V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000437600
Start 102277956:102277956(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1571G>T
AA Mutation p.Arg524Leu(p.R524L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence inframe_deletion
Transcription ID ENST00000292535
Start 102248898:102248909(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.4376_4387delTTTTCGGCCTCC
AA Mutation p.Leu1459_Leu1462del(p.L1459_L1462del)
Mutation Classification In_Frame_Del
Feature Type Transcript