Primary Site >> Liver Cancer

Gene >> PHGDH

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000369409
Start 119741851:119741851(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370627997
CDS Mutation c.1163T>C
AA Mutation p.Val388Ala(p.V388A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000369409
Start 119744025:119744025(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1587C>G
AA Mutation p.Phe529Leu(p.F529L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000369409
Start 119741864:119741864(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1176C>A
AA Mutation p.Asn392Lys(p.N392K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000369409
Start 119723436:119723436(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.351G>C
Mutation Classification Silent
Feature Type Transcript