Search Results: 1 genotypes retrieved

Data download

c.30C>T

p.Phe10Phe
Mutation type:Point Mutation effect:Silent Nucleotide number:30
Genome location:Exon2 Subdomain:Signal peptide
Alpha missense prediction value: Alpha missense prediction class:
No. of patients reported: 7
Patient information: Monoallelic variation (7); 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 64 hetero NA 49 NA I Other VTE (53) 53 Spain thrombosis (Other VTE) PMID: 31254973
2 NA 40 hetero NA 45 NA I Other VTE (19) 19 Spain thrombosis (Other VTE) PMID: 31254973
3 NA NA hetero NA NA NA I NA NA Spain NA PMID: 31254973
4 NA NA hetero NA NA NA I NA NA Spain NA PMID: 31254973
5 NA NA hetero NA NA NA I NA NA Spain NA PMID: 31254973
6 NA 9 hetero NA 74 NA I Other VTE (7) 7 Spain CVT (Other VTE) PMID: 31254973
7 NA NA hetero NA NA NA I NA NA Spain NA PMID: 31254973