NM_001077365.2(POMT1):c.891G>A (p.Leu297=) AND not specified
- Germline classification:
- Benign/Likely benign (4 submissions)
- Last evaluated:
- Jul 31, 2014
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000081496.20
Allele description [Variation Report for NM_001077365.2(POMT1):c.891G>A (p.Leu297=)]
NM_001077365.2(POMT1):c.891G>A (p.Leu297=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 13, 2025