NM_002495.4(NDUFS4):c.47G>T (p.Arg16Leu) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 5, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003313458.1
Allele description [Variation Report for NM_002495.4(NDUFS4):c.47G>T (p.Arg16Leu)]
NM_002495.4(NDUFS4):c.47G>T (p.Arg16Leu)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Oct 14, 2023