Deletion | NM_000297.4(PKD2):c.2524del (p.Leu842fs) | PKD2 | Pathogenic | 4 | 88995964 | 88995964 | GC | G | criteria provided, single submitter | ClinGen:CA645509148 |
Deletion | NM_000297.4(PKD2):c.481_502del (p.Gly161fs) | PKD2 | Pathogenic | 4 | 88929362 | 88929383 | ACCAGGGCCCGCCGTGCCCCAGC | A | criteria provided, single submitter | ClinGen:CA645509147 |
Deletion | NM_000297.4(PKD2):c.2159del (p.Asn720fs) | PKD2 | Pathogenic | 4 | 88986559 | 88986559 | GA | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA3004147 |
single nucleotide variant | NM_000297.4(PKD2):c.2523-1G>A | PKD2 | Pathogenic | 4 | 88995963 | 88995963 | G | A | criteria provided, single submitter | ClinGen:CA357627494 |
Deletion | NM_001009944.3(PKD1):c.11912del (p.Pro3971fs) | PKD1 | Pathogenic | 16 | 2140976 | 2140976 | CG | C | criteria provided, single submitter | ClinGen:CA645509208 |
single nucleotide variant | NM_001009944.3(PKD1):c.11713-1G>A | PKD1 | Pathogenic/Likely pathogenic | 16 | 2141176 | 2141176 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA394330362 |
Deletion | NM_001009944.3(PKD1):c.11538-2del | PKD1 | Pathogenic | 16 | 2141600 | 2141600 | CT | C | criteria provided, single submitter | ClinGen:CA645509210 |
single nucleotide variant | NM_001009944.3(PKD1):c.11156G>A (p.Arg3719Gln) | PKD1 | Pathogenic | 16 | 2142955 | 2142955 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA394336677 |
Deletion | NM_001009944.3(PKD1):c.9994del (p.Val3332fs) | PKD1 | Pathogenic | 16 | 2149701 | 2149701 | AC | A | criteria provided, single submitter | ClinGen:CA645509217 |
single nucleotide variant | NM_001009944.3(PKD1):c.8905C>T (p.Gln2969Ter) | PKD1 | Pathogenic | 16 | 2152858 | 2152858 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA394361576 |