Primary Site >> Liver Cancer

Gene >> EP300

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000263253
Start 41127626:41127626(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1046A>G
AA Mutation p.His349Arg(p.H349R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000263253
Start 41177033:41177033(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5322A>T
AA Mutation p.Lys1774Asn(p.K1774N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000263253
Start 41164088:41164088(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3764A>T
AA Mutation p.His1255Leu(p.H1255L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000263253
Start 41149765:41149765(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2384A>G
AA Mutation p.Gln795Arg(p.Q795R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000263253
Start 41178909:41178909(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7198T>A
AA Mutation p.Ser2400Thr(p.S2400T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000263253
Start 41173708:41173708(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4703A>G
AA Mutation p.Lys1568Arg(p.K1568R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000263253
Start 41172571:41172571(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4525T>A
AA Mutation p.Trp1509Arg(p.W1509R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000263253
Start 41151908:41151908(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2893C>G
AA Mutation p.Gln965Glu(p.Q965E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000263253
Start 41178167:41178167(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6456G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000263253
Start 41178842:41178842(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7131T>C
Mutation Classification Silent
Feature Type Transcript