NM_174936.4(PCSK9):c.1782C>T (p.Ala594=) AND Cardiovascular phenotype
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 16, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002404119.2
Allele description [Variation Report for NM_174936.4(PCSK9):c.1782C>T (p.Ala594=)]
NM_174936.4(PCSK9):c.1782C>T (p.Ala594=)
Condition(s)
- Name:
- Cardiovascular phenotype
- Identifiers:
- MedGen: CN230736
-
PREDICTED: LOW QUALITY PROTEIN: dnaJ homolog subfamily B member 6 [Equus przewal...
PREDICTED: LOW QUALITY PROTEIN: dnaJ homolog subfamily B member 6 [Equus przewalskii]gi|664752005|ref|XP_008533449.1|Protein
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Last Updated: May 1, 2024