NM_001017980.4(VMA21):c.255T>C (p.Tyr85=) AND X-linked myopathy with excessive autophagy
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Dec 20, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001511018.8
Allele description [Variation Report for NM_001017980.4(VMA21):c.255T>C (p.Tyr85=)]
NM_001017980.4(VMA21):c.255T>C (p.Tyr85=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024