Primary Site >> Liver Cancer

Gene >> ACPP

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000336375
Start 132342574:132342574(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.578A>G
AA Mutation p.Lys193Arg(p.K193R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000351273
Start 132367779:132367779(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1214G>C
AA Mutation p.Arg405Pro(p.R405P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000336375
Start 132356721:132356721(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148218296
CDS Mutation c.1004C>T
AA Mutation p.Thr335Met(p.T335M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000336375
Start 132331660:132331660(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.230A>T
AA Mutation p.Gln77Leu(p.Q77L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000336375
Start 132356730:132356730(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1013A>T
AA Mutation p.Glu338Val(p.E338V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000336375
Start 132352743:132352743(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.888A>C
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000336375
Start 132342623:132342623(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.627C>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000336375
Start 132342550:132342550(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.556-2A>C
Mutation Classification Splice_Site
Feature Type Transcript