Primary Site >> Liver Cancer

Gene >> DPYD

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000370192
Start 97699540:97699540(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.491A>C
AA Mutation p.Lys164Thr(p.K164T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000370192
Start 97699442:97699442(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.589C>T
AA Mutation p.Pro197Ser(p.P197S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000370192
Start 97549637:97549637(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs141439344
CDS Mutation c.1447G>A
AA Mutation p.Val483Ile(p.V483I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000370192
Start 97515766:97515766(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1700G>T
AA Mutation p.Gly567Val(p.G567V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000370192
Start 97549711:97549711(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1373G>A
AA Mutation p.Arg458Lys(p.R458K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000370192
Start 97098497:97098497(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2758A>G
AA Mutation p.Thr920Ala(p.T920A)
Mutation Classification Missense_Mutation
Feature Type Transcript