Primary Site >> Stomach Cancer

Gene >> EGLN2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000303961
Start 40801221:40801221(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.649G>A
AA Mutation p.Gly217Arg(p.G217R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000303961
Start 40800886:40800886(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.314A>G
AA Mutation p.Gln105Arg(p.Q105R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000303961
Start 40801219:40801219(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.647G>A
AA Mutation p.Gly216Asp(p.G216D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000303961
Start 40807512:40807512(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1129G>A
AA Mutation p.Ala377Thr(p.A377T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000303961
Start 40800899:40800899(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.327C>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000303961
Start 40800878:40800878(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.309delG
AA Mutation p.Cys104AlafsTer47(p.C104Afs*47)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000303961
Start 40800760:40800760(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.192delC
AA Mutation p.Arg65GlufsTer86(p.R65Efs*86)
Mutation Classification Frame_Shift_Del
Feature Type Transcript