Deletion | NM_001009944.3(PKD1):c.6583_6589del (p.Cys2195fs) | PKD1 | Pathogenic | 16 | 2158579 | 2158585 | CGCTGGCA | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA645509211 |
single nucleotide variant | NM_001009944.3(PKD1):c.4258G>T (p.Glu1420Ter) | PKD1 | Pathogenic | 16 | 2160910 | 2160910 | C | A | criteria provided, single submitter | ClinGen:CA394380975 |
single nucleotide variant | NM_001009944.3(PKD1):c.3285C>A (p.Tyr1095Ter) | PKD1 | Pathogenic | 16 | 2162351 | 2162351 | G | T | criteria provided, single submitter | ClinGen:CA394383399 |
single nucleotide variant | NM_001009944.3(PKD1):c.2932C>T (p.Gln978Ter) | PKD1 | Pathogenic | 16 | 2163215 | 2163215 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA394385563 |
single nucleotide variant | NM_001009944.3(PKD1):c.2152C>T (p.Gln718Ter) | PKD1 | Pathogenic | 16 | 2164872 | 2164872 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA394389261 |
single nucleotide variant | NM_001009944.3(PKD1):c.8704C>T (p.Gln2902Ter) | PKD1 | Pathogenic | 16 | 2153354 | 2153354 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA394362329 |
Deletion | NM_001009944.3(PKD1):c.12230_12239del (p.Ala4077fs) | PKD1 | Likely pathogenic | 16 | 2140491 | 2140500 | CCAGGACTCGG | C | criteria provided, single submitter | ClinGen:CA658653829 |
Deletion | NM_000297.4(PKD2):c.514del (p.Asp172fs) | PKD2 | Pathogenic | 4 | 88929396 | 88929396 | CG | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA658657391 |
single nucleotide variant | NM_000297.4(PKD2):c.603G>A (p.Trp201Ter) | PKD2 | Pathogenic | 4 | 88940617 | 88940617 | G | A | criteria provided, single submitter | ClinGen:CA357628188 |
single nucleotide variant | NM_000297.4(PKD2):c.964C>T (p.Arg322Trp) | PKD2 | Pathogenic/Likely pathogenic | 4 | 88959523 | 88959523 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA357632796 |