NM_001015878.2(AURKC):c.396G>A (p.Leu132=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Apr 3, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000891218.3
Allele description [Variation Report for NM_001015878.2(AURKC):c.396G>A (p.Leu132=)]
NM_001015878.2(AURKC):c.396G>A (p.Leu132=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Dec 24, 2023