Deletion | NM_138694.4(PKHD1):c.1205del (p.Phe402fs) | PKHD1 | Likely pathogenic | 6 | 51924754 | 51924754 | GA | G | criteria provided, single submitter | ClinGen:CA16041070 |
single nucleotide variant | NM_138694.4(PKHD1):c.748C>T (p.Gln250Ter) | PKHD1 | Likely pathogenic | 6 | 51934285 | 51934285 | G | A | criteria provided, single submitter | ClinGen:CA16041071 |
single nucleotide variant | NM_138694.4(PKHD1):c.603-2A>G | PKHD1 | Likely pathogenic | 6 | 51935870 | 51935870 | T | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA3853845 |
Deletion | NM_138694.4(PKHD1):c.527+1del | PKHD1 | Likely pathogenic | 6 | 51938260 | 51938260 | AC | A | criteria provided, single submitter | ClinGen:CA16041072 |
single nucleotide variant | NM_138694.4(PKHD1):c.448+2T>C | PKHD1 | Likely pathogenic | 6 | 51941072 | 51941072 | A | G | criteria provided, single submitter | ClinGen:CA16041073 |
Duplication | NM_138694.4(PKHD1):c.156dup (p.Asn53fs) | PKHD1 | Likely pathogenic | 6 | 51947314 | 51947315 | T | TG | criteria provided, single submitter | ClinGen:CA16041074 |
Deletion | NM_138694.4(PKHD1):c.4_7del (p.Thr2fs) | PKHD1 | Likely pathogenic | 6 | 51949725 | 51949728 | GCAGT | G | criteria provided, single submitter | ClinGen:CA16041075 |
Duplication | NM_001009944.3(PKD1):c.11251_11265dup (p.Gln3751_Gln3755dup) | PKD1 | Likely pathogenic | 16 | 2142484 | 2142485 | C | CCTGCAGCCGCACCTG | criteria provided, single submitter | ClinGen:CA16042936 |
single nucleotide variant | NM_001009944.3(PKD1):c.1523G>T (p.Cys508Phe) | PKD1 | Likely pathogenic | 16 | 2166917 | 2166917 | C | A | criteria provided, single submitter | ClinGen:CA16042982 |
Deletion | NM_001009944.3(PKD1):c.8369del (p.Pro2790fs) | PKD1 | Pathogenic/Likely pathogenic | 16 | 2153689 | 2153689 | CG | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA16043003 |