Primary Site >> Liver Cancer

Gene >> FOXG1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000313071
Start 28768210:28768210(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.931T>A
AA Mutation p.Ser311Thr(p.S311T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000313071
Start 28768359:28768359(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1080C>A
AA Mutation p.Asn360Lys(p.N360K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000313071
Start 28768142:28768142(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.863G>A
AA Mutation p.Arg288His(p.R288H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000313071
Start 28768506:28768506(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1227G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000313071
Start 28767777:28767777(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.498G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000313071
Start 28768011:28768011(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.732C>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence stop_gained
Transcription ID ENST00000313071
Start 28767685:28767685(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.406G>T
AA Mutation p.Glu136Ter(p.E136*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript