single nucleotide variant | NM_007217.4(PDCD10):c.474+5G>A | PDCD10 | Pathogenic/Likely pathogenic | 3 | 167405398 | 167405398 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA658657344 |
single nucleotide variant | NM_007217.4(PDCD10):c.475-1G>A | PDCD10 | Pathogenic | 3 | 167405105 | 167405105 | C | T | criteria provided, single submitter | OMIM:609118.0006 |
single nucleotide variant | NM_007217.4(PDCD10):c.496G>T (p.Glu166Ter) | PDCD10 | Likely pathogenic | 3 | 167405083 | 167405083 | C | A | criteria provided, single submitter | - |
Deletion | NM_007217.4(PDCD10):c.501del (p.Phe167fs) | PDCD10 | Likely pathogenic | 3 | 167405078 | 167405078 | CA | C | criteria provided, single submitter | - |
single nucleotide variant | NM_007217.4(PDCD10):c.510C>G (p.Tyr170Ter) | PDCD10 | Pathogenic/Likely pathogenic | 3 | 167405069 | 167405069 | G | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA355154090 |
single nucleotide variant | NM_007217.4(PDCD10):c.558-2A>T | PDCD10 | Likely pathogenic | 3 | 167402179 | 167402179 | T | A | criteria provided, single submitter | - |
single nucleotide variant | NM_007217.4(PDCD10):c.558-2A>C | PDCD10 | Pathogenic | 3 | 167402179 | 167402179 | T | G | criteria provided, single submitter | ClinGen:CA355153966 |
Duplication | NM_007217.4(PDCD10):c.584dup (p.Asn195fs) | PDCD10 | Pathogenic/Likely pathogenic | 3 | 167402150 | 167402151 | G | GT | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_007217.4(PDCD10):c.586C>T (p.Arg196Ter) | PDCD10 | Pathogenic | 3 | 167402149 | 167402149 | G | A | criteria provided, multiple submitters, no conflicts | - |
Deletion | NC_000007.14:g.(?_92240973)_(92242155_?)del | KRIT1 | Pathogenic | 7 | 91870287 | 91871469 | na | na | criteria provided, single submitter | - |