single nucleotide variant | NM_000304.4(PMP22):c.418T>A (p.Trp140Arg) | PMP22 | Likely pathogenic | 17 | 15134299 | 15134299 | A | T | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_000304.4(PMP22):c.390C>G (p.Tyr130Ter) | PMP22 | Likely pathogenic | 17 | 15134327 | 15134327 | G | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA398739656 |
single nucleotide variant | NM_000304.4(PMP22):c.228C>G (p.Ser76Arg) | PMP22 | Likely pathogenic | 17 | 15142879 | 15142879 | G | C | criteria provided, single submitter | ClinGen:CA398268148 |
single nucleotide variant | NM_000304.4(PMP22):c.431C>G (p.Pro144Arg) | PMP22 | Likely pathogenic | 17 | 15134286 | 15134286 | G | C | criteria provided, single submitter | ClinGen:CA398739549 |
single nucleotide variant | NM_000304.4(PMP22):c.235T>A (p.Ser79Thr) | PMP22 | Likely pathogenic | 17 | 15142872 | 15142872 | A | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA279110 |
single nucleotide variant | NM_000304.4(PMP22):c.199G>A (p.Ala67Thr) | PMP22 | Likely pathogenic | 17 | 15142908 | 15142908 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA254388,UniProtKB:Q01453#VAR_029965,OMIM:601097.0017 |
single nucleotide variant | NM_000304.4(PMP22):c.82T>C (p.Trp28Arg) | PMP22 | Likely pathogenic | 17 | 15162507 | 15162507 | A | G | criteria provided, single submitter | ClinGen:CA342724,UniProtKB:Q01453#VAR_029963,OMIM:601097.0014 |