Primary Site >> Liver Cancer

Gene >> EGLN2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000303961
Start 40801224:40801224(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140368149
CDS Mutation c.652C>T
AA Mutation p.Arg218Cys(p.R218C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000303961
Start 40807265:40807265(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1091A>G
AA Mutation p.Tyr364Cys(p.Y364C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000303961
Start 40801408:40801408(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.836G>T
AA Mutation p.Arg279Leu(p.R279L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000303961
Start 40800845:40800845(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.273G>A
Mutation Classification Silent
Feature Type Transcript