NM_001737.5(C9):c.1112G>C (p.Gly371Ala) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 16, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003831537.1
Allele description [Variation Report for NM_001737.5(C9):c.1112G>C (p.Gly371Ala)]
NM_001737.5(C9):c.1112G>C (p.Gly371Ala)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 5, 2024