Primary Site >> Stomach Cancer

Gene >> TYMP

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000252029
Start 50527710:50527710(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772830245
CDS Mutation c.524T>C
AA Mutation p.Val175Ala(p.V175A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000252029
Start 50529282:50529282(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.271C>G
AA Mutation p.Leu91Val(p.L91V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000252029
Start 50529166:50529166(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773716239
CDS Mutation c.387C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000252029
Start 50527234:50527234(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.696G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000252029
Start 50529554:50529554(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.156G>A
Mutation Classification Silent
Feature Type Transcript