NM_181723.3(MICU3):c.206T>G (p.Val69Gly) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 23, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004419722.1
Allele description [Variation Report for NM_181723.3(MICU3):c.206T>G (p.Val69Gly)]
NM_181723.3(MICU3):c.206T>G (p.Val69Gly)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 7, 2024