Primary Site >> Stomach Cancer

Gene >> GPX3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000388825
Start 151027517:151027517(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.445T>C
AA Mutation p.Tyr149His(p.Y149H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000388825
Start 151020737:151020737(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.83C>T
AA Mutation p.Ser28Leu(p.S28L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000388825
Start 151020680:151020680(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.26G>A
AA Mutation p.Cys9Tyr(p.C9Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000388825
Start 151028028:151028028(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.579A>G
AA Mutation p.Ile193Met(p.I193M)
Mutation Classification Missense_Mutation
Feature Type Transcript