Search Results: 1 genotypes retrieved

Data download

c.917insTGGC

p.(Gln307GlyfsX67)
Mutation type:Insertion Mutation effect:Frameshift Nucleotide number:917
Genome location:Exon9 Subdomain:Serine protease
Alpha missense prediction value: Alpha missense prediction class:
No. of patients reported: 1
Patient information: Monoallelic variation (1); Biallelic variation (0)
Patient Sex Age Genotype PC: amidolytic act (%) PC: clotting act (%) PC: Ag (%) PCD type Clinical presentation (age) First onset age Country Comments Reference
1 NA NA hetero NA 37 NA I Other VTE NA Netherlands NA PMID: 7482420