Primary Site >> Liver Cancer

Gene >> PTGER3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000306666
Start 71012454:71012454(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.928A>T
AA Mutation p.Thr310Ser(p.T310S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000306666
Start 71046803:71046803(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.775C>T
AA Mutation p.Arg259Cys(p.R259C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000306666
Start 71047129:71047129(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.449C>T
AA Mutation p.Ala150Val(p.A150V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000306666
Start 71012459:71012459(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.923A>T
AA Mutation p.Asn308Ile(p.N308I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000306666
Start 71046952:71046952(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.626T>A
AA Mutation p.Phe209Tyr(p.F209Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000306666
Start 71047361:71047361(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.217G>T
AA Mutation p.Val73Leu(p.V73L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000356595
Start 70952978:70952978(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1186A>C
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000306666
Start 70971734:70971734(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1170-1G>A
Mutation Classification Splice_Site
Feature Type Transcript