NM_013382.7(POMT2):c.1274G>C (p.Ser425Thr) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 30, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002535935.2
Allele description [Variation Report for NM_013382.7(POMT2):c.1274G>C (p.Ser425Thr)]
NM_013382.7(POMT2):c.1274G>C (p.Ser425Thr)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Sep 29, 2024