NM_001377458.1(CLCC1):c.1226A>C (p.Gln409Pro) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 4, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001228450.7
Allele description [Variation Report for NM_001377458.1(CLCC1):c.1226A>C (p.Gln409Pro)]
NM_001377458.1(CLCC1):c.1226A>C (p.Gln409Pro)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024