Primary Site >> Liver Cancer

Gene >> SCIN

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000297029
Start 12626603:12626603(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1001G>C
AA Mutation p.Gly334Ala(p.G334A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000297029
Start 12626617:12626617(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1015A>C
AA Mutation p.Ile339Leu(p.I339L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000297029
Start 12644695:12644695(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1871G>T
AA Mutation p.Gly624Val(p.G624V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000297029
Start 12570817:12570817(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.31G>T
AA Mutation p.Ala11Ser(p.A11S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000297029
Start 12578071:12578071(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.207G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000297029
Start 12570864:12570864(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.78G>A
Mutation Classification Silent
Feature Type Transcript