NM_004553.6(NDUFS6):c.96C>A (p.Val32=) AND not provided
- Germline classification:
- Benign/Likely benign (3 submissions)
- Last evaluated:
- Feb 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000677074.14
Allele description [Variation Report for NM_004553.6(NDUFS6):c.96C>A (p.Val32=)]
NM_004553.6(NDUFS6):c.96C>A (p.Val32=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 30, 2024