single nucleotide variant | NM_000297.4(PKD2):c.1390C>T (p.Arg464Ter) | PKD2 | Pathogenic | 4 | 88967864 | 88967864 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA123164,OMIM:173910.0005 |
single nucleotide variant | NM_000297.4(PKD2):c.2224C>T (p.Arg742Ter) | PKD2 | Pathogenic | 4 | 88986631 | 88986631 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA123160,OMIM:173910.0002 |
single nucleotide variant | NM_000297.4(PKD2):c.1139G>A (p.Trp380Ter) | PKD2 | Pathogenic | 4 | 88964429 | 88964429 | G | A | criteria provided, single submitter | ClinGen:CA123158,OMIM:173910.0001 |
single nucleotide variant | NM_016306.6(DNAJB11):c.616C>T (p.Arg206Ter) | DNAJB11 | Pathogenic | 3 | 186299800 | 186299800 | C | T | criteria provided, multiple submitters, no conflicts | OMIM:611341.0005 |
single nucleotide variant | NM_016306.6(DNAJB11):c.230T>C (p.Leu77Pro) | DNAJB11 | Likely pathogenic | 3 | 186293633 | 186293633 | T | C | criteria provided, single submitter | OMIM:611341.0004 |
single nucleotide variant | NM_016306.6(DNAJB11):c.161C>G (p.Pro54Arg) | DNAJB11 | Likely pathogenic | 3 | 186289976 | 186289976 | C | G | criteria provided, single submitter | OMIM:611341.0001 |
single nucleotide variant | NM_173543.3(DZIP1L):c.463C>T (p.Gln155Ter) | DZIP1L | Pathogenic | 3 | 137822351 | 137822351 | G | A | criteria provided, single submitter | ClinGen:CA354681055,OMIM:617570.0003 |