NM_006796.3(AFG3L2):c.2101G>A (p.Val701Ile) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 1, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000999531.20
Allele description [Variation Report for NM_006796.3(AFG3L2):c.2101G>A (p.Val701Ile)]
NM_006796.3(AFG3L2):c.2101G>A (p.Val701Ile)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Aug 4, 2024