NM_004320.6(ATP2A1):c.1800G>A (p.Leu600=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 15, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000604257.1
Allele description [Variation Report for NM_004320.6(ATP2A1):c.1800G>A (p.Leu600=)]
NM_004320.6(ATP2A1):c.1800G>A (p.Leu600=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 13, 2024