Primary Site >> Liver Cancer

Gene >> PHC3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000494943
Start 170128839:170128839(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1597C>G
AA Mutation p.Gln533Glu(p.Q533E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000494943
Start 170102875:170102875(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2492A>T
AA Mutation p.Asn831Ile(p.N831I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000494943
Start 170122675:170122675(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1822A>C
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000494943
Start 170149245:170149245(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.379-1G>C
Mutation Classification Splice_Site
Feature Type Transcript
ID 5
Mutation Consequence inframe_deletion
Transcription ID ENST00000494943
Start 170136594:170136617(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.685_708delTCACAGAATGGTCCACCAAAAAGC
AA Mutation p.Ser229_Ser236del(p.S229_S236del)
Mutation Classification In_Frame_Del
Feature Type Transcript