Insertion | NM_003482.4(KMT2D):c.15920_15921insT (p.Leu5308fs) | KMT2D | Likely pathogenic | 12 | 49418593 | 49418594 | T | TA | criteria provided, single submitter | ClinGen:CA658683787 |
single nucleotide variant | NM_001291415.2(KDM6A):c.748+1G>A | KDM6A | Likely pathogenic | X | 44911048 | 44911048 | G | A | criteria provided, single submitter | ClinGen:CA412778803 |
single nucleotide variant | NM_003482.4(KMT2D):c.49+2T>A | KMT2D | Likely pathogenic | 12 | 49449057 | 49449057 | A | T | criteria provided, single submitter | ClinGen:CA384691171 |
single nucleotide variant | NM_001291415.2(KDM6A):c.3835T>C (p.Trp1279Arg) | KDM6A | Likely pathogenic | X | 44949118 | 44949118 | T | C | criteria provided, single submitter | ClinGen:CA16621408 |
single nucleotide variant | NM_001291415.2(KDM6A):c.3754C>T (p.Leu1252Phe) | KDM6A | Likely pathogenic | X | 44949037 | 44949037 | C | T | criteria provided, single submitter | ClinGen:CA16609406 |
single nucleotide variant | NM_003482.4(KMT2D):c.16012T>C (p.Cys5338Arg) | KMT2D | Likely pathogenic | 12 | 49418401 | 49418401 | A | G | criteria provided, single submitter | ClinGen:CA16606557 |
single nucleotide variant | NM_003482.4(KMT2D):c.15467A>G (p.Tyr5156Cys) | KMT2D | Likely pathogenic | 12 | 49420282 | 49420282 | T | C | criteria provided, single submitter | ClinGen:CA16606292 |
single nucleotide variant | NM_003482.4(KMT2D):c.2T>C (p.Met1Thr) | KMT2D | Likely pathogenic | 12 | 49449106 | 49449106 | A | G | criteria provided, single submitter | ClinGen:CA16603307 |
single nucleotide variant | NM_001291415.2(KDM6A):c.2356A>G (p.Thr786Ala) | KDM6A | Likely pathogenic | X | 44929100 | 44929100 | A | G | criteria provided, single submitter | ClinGen:CA10392500 |
single nucleotide variant | NM_001291415.2(KDM6A):c.3791A>G (p.Gln1264Arg) | KDM6A | Likely pathogenic | X | 44949074 | 44949074 | A | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA206562 |