Primary Site >> Liver Cancer

Gene >> XRN2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000377191
Start 21365437:21365437(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2272C>T
AA Mutation p.Pro758Ser(p.P758S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000377191
Start 21332300:21332300(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.718G>A
AA Mutation p.Gly240Ser(p.G240S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000377191
Start 21348389:21348389(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1822A>T
AA Mutation p.Asn608Tyr(p.N608Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000377191
Start 21331782:21331782(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.664G>T
AA Mutation p.Asp222Tyr(p.D222Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000377191
Start 21389308:21389308(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2823A>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000377191
Start 21382043:21382043(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2634G>A
Mutation Classification Silent
Feature Type Transcript