Primary Site >> Liver Cancer

Gene >> CTNND1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000399050
Start 57810165:57810165(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2492G>T
AA Mutation p.Gly831Val(p.G831V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000399050
Start 57808225:57808225(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2024G>A
AA Mutation p.Ser675Asn(p.S675N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000399050
Start 57791558:57791558(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.80C>T
AA Mutation p.Thr27Ile(p.T27I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000399050
Start 57802051:57802051(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759069892
CDS Mutation c.1275C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000399050
Start 57815920:57815920(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773613029
CDS Mutation c.2814C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence stop_gained
Transcription ID ENST00000399050
Start 57810164:57810164(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2491G>T
AA Mutation p.Gly831Ter(p.G831*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript