Primary Site >> Liver Cancer

Gene >> SLC34A2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000382051
Start 25676738:25676738(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2062A>G
AA Mutation p.Thr688Ala(p.T688A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000382051
Start 25669694:25669694(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.683T>A
AA Mutation p.Val228Glu(p.V228E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000382051
Start 25662747:25662747(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374467761
CDS Mutation c.155C>T
AA Mutation p.Pro52Leu(p.P52L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000382051
Start 25674563:25674563(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1392C>G
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000382051
Start 25666177:25666177(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.429T>A
Mutation Classification Silent
Feature Type Transcript