Primary Site >> Liver Cancer

Gene >> SLC38A2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000256689
Start 46366919:46366919(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.508A>G
AA Mutation p.Lys170Glu(p.K170E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000256689
Start 46364493:46364493(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746626410
CDS Mutation c.769A>G
AA Mutation p.Ile257Val(p.I257V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000256689
Start 46361176:46361176(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1456A>G
AA Mutation p.Met486Val(p.M486V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000256689
Start 46367158:46367158(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.399A>G
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000256689
Start 46370595:46370595(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.231A>G
Mutation Classification Silent
Feature Type Transcript