Primary Site >> Liver Cancer

Gene >> PTPRD

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8500869:8500869(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2013A>C
AA Mutation p.Lys671Asn(p.K671N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8341889:8341889(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4751A>T
AA Mutation p.His1584Leu(p.H1584L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8636718:8636718(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.191T>G
AA Mutation p.Val64Gly(p.V64G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000356435
Start 8504350:8504350(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1733A>G
AA Mutation p.Asn578Ser(p.N578S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000356435
Start 8527349:8527349(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.546T>C
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000356435
Start 8733790:8733790(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.54G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000356435
Start 8486105:8486105(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2712G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000356435
Start 8404601:8404601(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4146A>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000356435
Start 8341939:8341939(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4701T>C
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000356435
Start 8521421:8521421(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.817delG
AA Mutation p.Ala273GlnfsTer4(p.A273Qfs*4)
Mutation Classification Frame_Shift_Del
Feature Type Transcript