Primary Site >> Stomach Cancer

Gene >> OTX1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000282549
Start 63056069:63056069(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.818C>T
AA Mutation p.Ala273Val(p.A273V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000282549
Start 63053040:63053040(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.50T>G
AA Mutation p.Leu17Arg(p.L17R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000282549
Start 63055963:63055963(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.712C>T
AA Mutation p.Pro238Ser(p.P238S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000282549
Start 63054151:63054151(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.202C>T
AA Mutation p.Arg68Trp(p.R68W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000282549
Start 63055827:63055827(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199519181
CDS Mutation c.576G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000282549
Start 63056010:63056010(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.759G>A
Mutation Classification Silent
Feature Type Transcript