NM_002775.5(HTRA1):c.283G>T (p.Val95Leu) AND Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 15, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002227771.1
Allele description [Variation Report for NM_002775.5(HTRA1):c.283G>T (p.Val95Leu)]
NM_002775.5(HTRA1):c.283G>T (p.Val95Leu)
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023