NM_001286577.2(C2CD3):c.1169G>A (p.Arg390Lys) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 25, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000969260.7
Allele description [Variation Report for NM_001286577.2(C2CD3):c.1169G>A (p.Arg390Lys)]
NM_001286577.2(C2CD3):c.1169G>A (p.Arg390Lys)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024