Primary Site >> Liver Cancer

Gene >> AXIN2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000307078
Start 65541532:65541532(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.982G>A
AA Mutation p.Gly328Ser(p.G328S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000307078
Start 65549583:65549583(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs139274803
CDS Mutation c.893A>G
AA Mutation p.Asn298Ser(p.N298S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000307078
Start 65537524:65537524(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1512C>G
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000307078
Start 65536477:65536477(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1984C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000307078
Start 65549646:65549647(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.829_830delAG
AA Mutation p.Ser277ArgfsTer4(p.S277Rfs*4)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000307078
Start 65557846:65557846(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.775delG
AA Mutation p.Ala259ArgfsTer3(p.A259Rfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 7
Mutation Consequence stop_gained
Transcription ID ENST00000307078
Start 65538208:65538208(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1195C>T
AA Mutation p.Arg399Ter(p.R399*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence stop_gained;splice_region_variant
Transcription ID ENST00000307078
Start 65538343:65538343(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1060A>T
AA Mutation p.Arg354Ter(p.R354*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript