NM_001397406.1(FDX2):c.441G>A (p.Ser147=) AND not provided
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Jan 26, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001521710.9
Allele description [Variation Report for NM_001397406.1(FDX2):c.441G>A (p.Ser147=)]
NM_001397406.1(FDX2):c.441G>A (p.Ser147=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 12, 2024