NM_000714.6(TSPO):c.41C>T (p.Ala14Val) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 29, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000963535.4
Allele description [Variation Report for NM_000714.6(TSPO):c.41C>T (p.Ala14Val)]
NM_000714.6(TSPO):c.41C>T (p.Ala14Val)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024