Duplication | NM_138694.4(PKHD1):c.10199dup (p.Met3400fs) | PKHD1 | Likely pathogenic | 6 | 51524724 | 51524725 | C | CA | criteria provided, single submitter | ClinGen:CA16041028 |
Deletion | NM_138694.4(PKHD1):c.10186_10190del (p.Tyr3396fs) | PKHD1 | Likely pathogenic | 6 | 51524734 | 51524738 | TTGGTA | T | criteria provided, single submitter | ClinGen:CA3851132 |
Duplication | NM_138694.4(PKHD1):c.10109dup (p.Phe3371fs) | PKHD1 | Pathogenic/Likely pathogenic | 6 | 51609229 | 51609230 | T | TA | criteria provided, multiple submitters, no conflicts | ClinGen:CA16041029 |
single nucleotide variant | NM_138694.4(PKHD1):c.9901G>T (p.Glu3301Ter) | PKHD1 | Pathogenic/Likely pathogenic | 6 | 51611616 | 51611616 | C | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA3851295 |
Duplication | NM_138694.4(PKHD1):c.9856_9859dup (p.Cys3287Ter) | PKHD1 | Likely pathogenic | 6 | 51611657 | 51611658 | C | CAACT | criteria provided, single submitter | ClinGen:CA16041030 |
Deletion | NM_138694.4(PKHD1):c.9743del (p.Phe3248fs) | PKHD1 | Likely pathogenic | 6 | 51612671 | 51612671 | GA | G | criteria provided, single submitter | ClinGen:CA3851347 |
single nucleotide variant | NM_138694.4(PKHD1):c.9718C>T (p.Arg3240Ter) | PKHD1 | Pathogenic/Likely pathogenic | 6 | 51612696 | 51612696 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA16041031 |
single nucleotide variant | NM_138694.4(PKHD1):c.9683C>A (p.Ser3228Ter) | PKHD1 | Pathogenic/Likely pathogenic | 6 | 51612731 | 51612731 | G | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA16041032 |
Duplication | NM_138694.4(PKHD1):c.9470_9473dup (p.Met3158fs) | PKHD1 | Likely pathogenic | 6 | 51612940 | 51612941 | C | CATGG | criteria provided, single submitter | ClinGen:CA16041033 |
Deletion | NM_138694.4(PKHD1):c.8958del (p.Gln2987fs) | PKHD1 | Likely pathogenic | 6 | 51613456 | 51613456 | GA | G | criteria provided, single submitter | ClinGen:CA16041034 |