Primary Site >> Stomach Cancer

Gene >> S1PR5

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000333430
Start 10513981:10513981(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1031C>T
AA Mutation p.Ala344Val(p.A344V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000333430
Start 10513826:10513826(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1186G>A
AA Mutation p.Ala396Thr(p.A396T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000333430
Start 10514042:10514042(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201928564
CDS Mutation c.970G>A
AA Mutation p.Gly324Arg(p.G324R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000333430
Start 10513872:10513872(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765367534
CDS Mutation c.1140C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000333430
Start 10514409:10514409(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.603C>T
Mutation Classification Silent
Feature Type Transcript