single nucleotide variant | NM_001009944.3(PKD1):c.10377C>G (p.Tyr3459Ter) | PKD1 | Likely pathogenic | 16 | 2147348 | 2147348 | G | C | criteria provided, single submitter | - |
Deletion | NM_001009944.3(PKD1):c.10247del (p.Gly3416fs) | PKD1 | Likely pathogenic | 16 | 2147478 | 2147478 | TC | T | criteria provided, single submitter | - |
Deletion | NM_001009944.3(PKD1):c.9826_9829del (p.Thr3276fs) | PKD1 | Likely pathogenic | 16 | 2149956 | 2149959 | CGAGT | C | criteria provided, single submitter | - |
single nucleotide variant | NM_001009944.3(PKD1):c.9431G>C (p.Gly3144Ala) | PKD1 | Likely pathogenic | 16 | 2150534 | 2150534 | C | G | criteria provided, single submitter | - |
single nucleotide variant | NM_001009944.3(PKD1):c.9298C>T (p.Gln3100Ter) | PKD1 | Pathogenic/Likely pathogenic | 16 | 2152161 | 2152161 | G | A | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_001009944.3(PKD1):c.8973C>A (p.Tyr2991Ter) | PKD1 | Pathogenic/Likely pathogenic | 16 | 2152610 | 2152610 | G | T | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_001009944.3(PKD1):c.8933T>C (p.Phe2978Ser) | PKD1 | Likely pathogenic | 16 | 2152830 | 2152830 | A | G | criteria provided, single submitter | - |
single nucleotide variant | NM_001009944.3(PKD1):c.7984C>T (p.Gln2662Ter) | PKD1 | Pathogenic/Likely pathogenic | 16 | 2155355 | 2155355 | G | A | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_001009944.3(PKD1):c.7915C>T (p.Arg2639Ter) | PKD1 | Pathogenic | 16 | 2155424 | 2155424 | G | A | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_001009944.3(PKD1):c.7856T>G (p.Leu2619Arg) | PKD1 | Likely pathogenic | 16 | 2155873 | 2155873 | A | C | criteria provided, single submitter | - |