Primary Site >> Liver Cancer

Gene >> VWF

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261405
Start 6034792:6034792(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2581C>T
AA Mutation p.His861Tyr(p.H861Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261405
Start 6031565:6031565(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2699G>A
AA Mutation p.Ser900Asn(p.S900N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000261405
Start 6034798:6034798(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371017187
CDS Mutation c.2575A>G
AA Mutation p.Thr859Ala(p.T859A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000261405
Start 6073697:6073697(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.919C>T
AA Mutation p.Pro307Ser(p.P307S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000261405
Start 5981974:5981974(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7099T>G
AA Mutation p.Cys2367Gly(p.C2367G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000261405
Start 6019233:6019233(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4185G>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000261405
Start 6121181:6121181(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.213G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000261405
Start 6016625:6016625(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5202G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000261405
Start 6036429:6036435(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2499_2505delCAAGGAG
AA Mutation p.Lys834MetfsTer7(p.K834Mfs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000261405
Start 6019412:6019412(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4006C>T
AA Mutation p.Arg1336Ter(p.R1336*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript