Primary Site >> Stomach Cancer

Gene >> PTGES2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000338961
Start 128124517:128124517(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751124073
CDS Mutation c.511G>A
AA Mutation p.Ala171Thr(p.A171T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000338961
Start 128122387:128122387(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.980G>A
AA Mutation p.Gly327Asp(p.G327D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000338961
Start 128122402:128122402(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779011818
CDS Mutation c.965G>A
AA Mutation p.Arg322Gln(p.R322Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000338961
Start 128123044:128123044(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201491985
CDS Mutation c.777G>A
Mutation Classification Silent
Feature Type Transcript