NM_001012302.3(ANO9):c.275C>A (p.Thr92Asn) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004172501.1
Allele description [Variation Report for NM_001012302.3(ANO9):c.275C>A (p.Thr92Asn)]
NM_001012302.3(ANO9):c.275C>A (p.Thr92Asn)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 2, 2024