NM_001372106.1(DNAH10):c.13026C>T (p.Leu4342=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004546152.2
Allele description
NM_001372106.1(DNAH10):c.13026C>T (p.Leu4342=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jun 17, 2024