Primary Site >> Stomach Cancer

Gene >> GMPR2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000355299
Start 24238771:24238771(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781312813
CDS Mutation c.1040C>T
AA Mutation p.Ala347Val(p.A347V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000355299
Start 24235789:24235789(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.260A>G
AA Mutation p.Glu87Gly(p.E87G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000355299
Start 24238391:24238391(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.843C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000355299
Start 24236128:24236128(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.453G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence stop_gained
Transcription ID ENST00000355299
Start 24238707:24238707(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.976G>T
AA Mutation p.Glu326Ter(p.E326*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript