single nucleotide variant | NM_000255.4(MMUT):c.281G>T (p.Gly94Val) | MMUT | Pathogenic | 6 | 49426899 | 49426899 | C | A | criteria provided, multiple submitters, no conflicts | - |
Deletion | NM_000255.4(MMUT):c.622del (p.Val208fs) | MMUT | Pathogenic | 6 | 49425535 | 49425535 | AC | A | criteria provided, single submitter | - |
single nucleotide variant | NM_000255.4(MMUT):c.947A>G (p.Tyr316Cys) | MMUT | Pathogenic/Likely pathogenic | 6 | 49421434 | 49421434 | T | C | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_000255.4(MMUT):c.753+1G>A | MMUT | Pathogenic/Likely pathogenic | 6 | 49425403 | 49425403 | C | T | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_000255.4(MMUT):c.567T>G (p.Asn189Lys) | MMUT | Likely pathogenic | 6 | 49425590 | 49425590 | A | C | criteria provided, single submitter | - |
single nucleotide variant | NM_000255.4(MMUT):c.1889G>C (p.Gly630Ala) | MMUT | Pathogenic/Likely pathogenic | 6 | 49407986 | 49407986 | C | G | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_000255.4(MMUT):c.912-1G>A | MMUT | Likely pathogenic | 6 | 49421470 | 49421470 | C | T | criteria provided, single submitter | - |
Duplication | NM_000255.4(MMUT):c.1148dup (p.Ser384fs) | MMUT | Pathogenic | 6 | 49419362 | 49419363 | C | CT | criteria provided, single submitter | - |
Duplication | NM_000255.4(MMUT):c.1885dup (p.Arg629fs) | MMUT | Pathogenic | 6 | 49407989 | 49407990 | C | CT | criteria provided, single submitter | - |
single nucleotide variant | NM_000255.4(MMUT):c.2020C>T (p.Leu674Phe) | MMUT | Likely pathogenic | 6 | 49403273 | 49403273 | G | A | criteria provided, single submitter | - |