Primary Site >> Liver Cancer

Gene >> INSIG1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000340368
Start 155302309:155302309(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.596G>A
AA Mutation p.Gly199Asp(p.G199D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000340368
Start 155302365:155302365(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.652G>A
AA Mutation p.Ala218Thr(p.A218T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000340368
Start 155302298:155302298(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.585C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000340368
Start 155301565:155301565(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.413-1G>C
Mutation Classification Splice_Site
Feature Type Transcript