Primary Site >> Liver Cancer

Gene >> PHIP

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000275034
Start 79017575:79017575(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1003T>C
AA Mutation p.Phe335Leu(p.F335L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000275034
Start 78970101:78970101(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3070G>C
AA Mutation p.Ala1024Pro(p.A1024P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000275034
Start 78947661:78947661(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4168A>T
AA Mutation p.Ser1390Cys(p.S1390C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000275034
Start 79060484:79060484(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.433A>T
AA Mutation p.Ser145Cys(p.S145C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000275034
Start 78955650:78955650(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148189504
CDS Mutation c.3815A>G
AA Mutation p.Tyr1272Cys(p.Y1272C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000275034
Start 78970146:78970146(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3025A>G
AA Mutation p.Ile1009Val(p.I1009V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000275034
Start 78982899:78982899(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2756A>T
AA Mutation p.Glu919Val(p.E919V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000275034
Start 79017493:79017493(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1085A>T
AA Mutation p.Glu362Val(p.E362V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000275034
Start 78978700:78978700(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2781G>C
Mutation Classification Silent
Feature Type Transcript