Primary Site >> Liver Cancer

Gene >> PDGFRA

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000257290
Start 54272486:54272486(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745702167
CDS Mutation c.1330G>C
AA Mutation p.Asp444His(p.D444H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000257290
Start 54273709:54273709(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1537G>A
AA Mutation p.Glu513Lys(p.E513K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000257290
Start 54290373:54290373(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775205485
CDS Mutation c.2941C>T
AA Mutation p.Arg981Cys(p.R981C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000257290
Start 54290469:54290469(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3037A>G
AA Mutation p.Ser1013Gly(p.S1013G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000257290
Start 54285857:54285857(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2456T>G
AA Mutation p.Leu819Arg(p.L819R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000257290
Start 54290434:54290434(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3002A>T
AA Mutation p.Lys1001Met(p.K1001M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000257290
Start 54290435:54290435(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3003G>T
AA Mutation p.Lys1001Asn(p.K1001N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000257290
Start 54277488:54277488(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1887A>G
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000257290
Start 54261330:54261330(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.285A>T
Mutation Classification Silent
Feature Type Transcript