Primary Site >> Stomach Cancer

Gene >> GNPDA1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000311337
Start 142006317:142006317(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767475273
CDS Mutation c.236G>A
AA Mutation p.Arg79Gln(p.R79Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000311337
Start 142004966:142004966(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746621093
CDS Mutation c.560C>T
AA Mutation p.Thr187Met(p.T187M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000311337
Start 142005054:142005054(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753033449
CDS Mutation c.472C>T
AA Mutation p.Arg158Cys(p.R158C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000311337
Start 142006200:142006200(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.353G>A
AA Mutation p.Cys118Tyr(p.C118Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000311337
Start 142002035:142002035(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766066425
CDS Mutation c.864C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000311337
Start 142005037:142005037(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.489C>T
Mutation Classification Silent
Feature Type Transcript