Primary Site >> Stomach Cancer

Gene >> P2RY2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000311131
Start 73234283:73234283(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372504224
CDS Mutation c.124G>A
AA Mutation p.Val42Met(p.V42M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000311131
Start 73234973:73234973(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.814C>T
AA Mutation p.Arg272Cys(p.R272C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000311131
Start 73234550:73234550(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.391C>T
AA Mutation p.Arg131Trp(p.R131W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000311131
Start 73234439:73234439(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.280G>A
AA Mutation p.Ala94Thr(p.A94T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000311131
Start 73235006:73235006(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs575826893
CDS Mutation c.847G>A
AA Mutation p.Ala283Thr(p.A283T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000311131
Start 73234690:73234690(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.531C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000311131
Start 73234279:73234279(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.120C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000311131
Start 73234282:73234282(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.123C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000311131
Start 73234568:73234568(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.409C>T
AA Mutation p.Arg137Ter(p.R137*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000311131
Start 73234477:73234477(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.318C>A
AA Mutation p.Cys106Ter(p.C106*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript