Primary Site >> Liver Cancer

Gene >> PIK3CA

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000263967
Start 179199081:179199081(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.256A>T
AA Mutation p.Thr86Ser(p.T86S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000263967
Start 179234297:179234297(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs121913279
CDS Mutation c.3140A>T
AA Mutation p.His1047Leu(p.H1047L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000263967
Start 179218304:179218304(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs121913274
CDS Mutation c.1634A>C
AA Mutation p.Glu545Ala(p.E545A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000263967
Start 179234312:179234312(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3155C>A
AA Mutation p.Thr1052Lys(p.T1052K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000263967
Start 179218294:179218294(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs121913273
CDS Mutation c.1624G>A
AA Mutation p.Glu542Lys(p.E542K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000263967
Start 179198938:179198938(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772110575
CDS Mutation c.113G>A
AA Mutation p.Arg38His(p.R38H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000263967
Start 179234297:179234297(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs121913279
CDS Mutation c.3140A>G
AA Mutation p.His1047Arg(p.H1047R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000263967
Start 179198904:179198904(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.79C>A
AA Mutation p.Pro27Thr(p.P27T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000263967
Start 179210438:179210438(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1412C>T
AA Mutation p.Pro471Leu(p.P471L)
Mutation Classification Missense_Mutation
Feature Type Transcript