single nucleotide variant | NM_003482.4(KMT2D):c.15921+1G>A | KMT2D | Likely pathogenic | 12 | 49418592 | 49418592 | C | T | criteria provided, single submitter | ClinGen:CA384682340 |
single nucleotide variant | NM_003482.4(KMT2D):c.840-2A>G | KMT2D | Likely pathogenic | 12 | 49447106 | 49447106 | T | C | criteria provided, single submitter | ClinGen:CA384680417 |
single nucleotide variant | NM_003482.4(KMT2D):c.10574T>C (p.Leu3525Pro) | KMT2D | Likely pathogenic | 12 | 49428016 | 49428016 | A | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA384728188,OMIM:602113.0010 |
single nucleotide variant | NM_003482.4(KMT2D):c.15854C>G (p.Pro5285Arg) | KMT2D | Likely pathogenic | 12 | 49418660 | 49418660 | G | C | criteria provided, single submitter | ClinGen:CA384683061 |
single nucleotide variant | NM_003482.4(KMT2D):c.16412G>A (p.Arg5471Lys) | KMT2D | Likely pathogenic | 12 | 49416063 | 49416063 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA384676632 |
single nucleotide variant | NM_003482.4(KMT2D):c.125C>T (p.Ser42Phe) | KMT2D | Likely pathogenic | 12 | 49448734 | 49448734 | G | A | criteria provided, single submitter | ClinGen:CA384690291 |
single nucleotide variant | NM_003482.4(KMT2D):c.10784A>G (p.Tyr3595Cys) | KMT2D | Likely pathogenic | 12 | 49427704 | 49427704 | T | C | criteria provided, single submitter | ClinGen:CA384726218 |
single nucleotide variant | NM_003482.4(KMT2D):c.10356-12G>A | KMT2D | Likely pathogenic | 12 | 49428461 | 49428461 | C | T | criteria provided, single submitter | ClinGen:CA645372912 |
single nucleotide variant | NM_003482.4(KMT2D):c.11800C>T (p.Gln3934Ter) | KMT2D | Likely pathogenic | 12 | 49426688 | 49426688 | G | A | criteria provided, single submitter | ClinGen:CA384715238 |
single nucleotide variant | NM_003482.4(KMT2D):c.14515+1G>T | KMT2D | Likely pathogenic | 12 | 49421791 | 49421791 | C | A | criteria provided, single submitter | ClinGen:CA384694833 |