Primary Site >> Liver Cancer

Gene >> FURIN

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000268171
Start 90880708:90880708(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1574C>T
AA Mutation p.Ala525Val(p.A525V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000268171
Start 90881375:90881375(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749641930
CDS Mutation c.1882A>G
AA Mutation p.Ser628Gly(p.S628G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000268171
Start 90880094:90880094(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1377A>T
AA Mutation p.Lys459Asn(p.K459N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000268171
Start 90880176:90880176(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1459G>A
AA Mutation p.Ala487Thr(p.A487T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000268171
Start 90881698:90881698(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762528103
CDS Mutation c.2205C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000268171
Start 90881470:90881470(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1977C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence stop_gained
Transcription ID ENST00000268171
Start 90879923:90879923(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1315C>T
AA Mutation p.Gln439Ter(p.Q439*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript