single nucleotide variant | NM_001009944.3(PKD1):c.8762A>G (p.His2921Arg) | PKD1 | Likely pathogenic | 16 | 2153296 | 2153296 | T | C | criteria provided, single submitter | ClinGen:CA394362115 |
single nucleotide variant | NM_001009944.3(PKD1):c.7861G>T (p.Glu2621Ter) | PKD1 | Pathogenic | 16 | 2155868 | 2155868 | C | A | criteria provided, single submitter | ClinGen:CA394367599 |
Deletion | NM_001009944.3(PKD1):c.896_897del (p.Pro299fs) | PKD1 | Pathogenic | 16 | 2168096 | 2168097 | CAG | C | criteria provided, single submitter | ClinGen:CA658798518 |
Deletion | NM_000297.4(PKD2):c.2284_2287del (p.Tyr762fs) | PKD2 | Pathogenic | 4 | 88986956 | 88986959 | AGTAC | A | criteria provided, single submitter | ClinGen:CA658796448 |
single nucleotide variant | NM_001009944.3(PKD1):c.12035G>A (p.Trp4012Ter) | PKD1 | Pathogenic | 16 | 2140778 | 2140778 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA7828865 |
single nucleotide variant | NM_001009944.3(PKD1):c.6877C>T (p.Pro2293Ser) | PKD1 | Likely pathogenic | 16 | 2158291 | 2158291 | G | A | criteria provided, single submitter | ClinGen:CA394372711 |
single nucleotide variant | NM_000297.4(PKD2):c.2533C>T (p.Arg845Ter) | PKD2 | Pathogenic | 4 | 88995974 | 88995974 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA3004284 |
single nucleotide variant | NM_001009944.3(PKD1):c.6031C>T (p.Gln2011Ter) | PKD1 | Pathogenic | 16 | 2159137 | 2159137 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA394374645 |
single nucleotide variant | NM_000297.4(PKD2):c.637C>T (p.Arg213Ter) | PKD2 | Pathogenic | 4 | 88940651 | 88940651 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA10575461 |
Indel | NM_138694.4(PKHD1):c.4352_4356delinsAAGGGGTCA (p.Pro1451fs) | PKHD1 | Pathogenic | 6 | 51890252 | 51890256 | CAAGG | TGACCCCTT | criteria provided, single submitter | ClinGen:CA658796770 |