Primary Site >> Pancreatic Cancer

Gene >> VWF

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261405
Start 6029382:6029382(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs181452677
CDS Mutation c.2927G>A
AA Mutation p.Arg976His(p.R976H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261405
Start 5971628:5971628(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368286307
CDS Mutation c.7519C>T
AA Mutation p.Arg2507Trp(p.R2507W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000261405
Start 6016101:6016101(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754062706
CDS Mutation c.5443G>A
AA Mutation p.Ala1815Thr(p.A1815T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000261405
Start 6019282:6019282(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773292982
CDS Mutation c.4136G>A
AA Mutation p.Arg1379His(p.R1379H)
Mutation Classification Missense_Mutation
Feature Type Transcript