Primary Site >> Stomach Cancer

Gene >> DHPS

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000210060
Start 12679696:12679696(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.518A>T
AA Mutation p.Asn173Ile(p.N173I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000210060
Start 12681610:12681610(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.157G>A
AA Mutation p.Gly53Ser(p.G53S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000210060
Start 12680261:12680261(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145815031
CDS Mutation c.272G>A
AA Mutation p.Arg91His(p.R91H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000210060
Start 12679529:12679529(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.606G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000210060
Start 12681629:12681629(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.138G>A
Mutation Classification Silent
Feature Type Transcript