Primary Site >> Liver Cancer

Gene >> PTGS2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000367468
Start 186679354:186679354(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.137G>A
AA Mutation p.Arg46Gln(p.R46Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000367468
Start 186679201:186679201(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764607381
CDS Mutation c.170C>T
AA Mutation p.Pro57Leu(p.P57L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000367468
Start 186676117:186676117(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1038A>G
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000367468
Start 186675391:186675391(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1263T>A
Mutation Classification Silent
Feature Type Transcript