Primary Site >> Liver Cancer

Gene >> ZNF185

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000370268
Start 152922219:152922219(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.700C>T
AA Mutation p.Pro234Ser(p.P234S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000370268
Start 152945449:152945449(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1391A>G
AA Mutation p.Glu464Gly(p.E464G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000370268
Start 152938145:152938145(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1190C>T
AA Mutation p.Ala397Val(p.A397V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000370268
Start 152959778:152959778(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1486G>T
AA Mutation p.Gly496Cys(p.G496C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000370268
Start 152932918:152932918(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1065G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000370268
Start 152917312:152917312(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.291C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence stop_gained
Transcription ID ENST00000370268
Start 152945445:152945445(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1387C>T
AA Mutation p.Arg463Ter(p.R463*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript