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_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.616C>T (p.Arg206Ter) | DNAJB11 | Pathogenic | 3 | 186299800 | 186299800 | C | T | criteria provided, multiple submitters, no conflicts | OMIM:611341.0005 |
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 |
Deletion | NM_198334.3(GANAB):c.1848_1849del (p.Asp618fs) | GANAB | Pathogenic | 11 | 62396753 | 62396754 | CCT | C | criteria provided, single submitter | ClinGen:CA10586208,OMIM:104160.0002 |
Deletion | NM_198334.3(GANAB):c.2624+2_2624+7del | GANAB | Pathogenic | 11 | 62393800 | 62393805 | CCCATTA | C | criteria provided, single submitter | ClinGen:CA10586210,OMIM:104160.0004 |
single nucleotide variant | NM_198334.3(GANAB):c.2449C>T (p.Arg817Trp) | GANAB | Likely pathogenic | 11 | 62394105 | 62394105 | G | A | criteria provided, single submitter | ClinGen:CA10586211,OMIM:104160.0005 |
single nucleotide variant | NM_198334.3(GANAB):c.2443C>T (p.Arg815Ter) | GANAB | Likely pathogenic | 11 | 62394111 | 62394111 | G | A | criteria provided, single submitter | - |
single nucleotide variant | NM_198334.3(GANAB):c.181C>T (p.Arg61Ter) | GANAB | Pathogenic | 11 | 62406902 | 62406902 | G | A | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_001009944.3(PKD1):c.12124C>T (p.Gln4042Ter) | PKD1 | Pathogenic | 16 | 2140689 | 2140689 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA119364,OMIM:601313.0002 |