Primary Site >> Liver Cancer

Gene >> GABRQ

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000598523
Start 152646985:152646985(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.344A>C
AA Mutation p.Lys115Thr(p.K115T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000598523
Start 152652661:152652661(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1279G>C
AA Mutation p.Ala427Pro(p.A427P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000598523
Start 152652581:152652581(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1199C>A
AA Mutation p.Pro400His(p.P400H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000598523
Start 152650494:152650494(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.815T>C
AA Mutation p.Val272Ala(p.V272A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000598523
Start 152649775:152649775(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.644G>C
AA Mutation p.Trp215Ser(p.W215S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000598523
Start 152649284:152649284(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.561G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000598523
Start 152638331:152638331(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.129C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence stop_gained
Transcription ID ENST00000598523
Start 152650536:152650536(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.857C>A
AA Mutation p.Ser286Ter(p.S286*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript