NM_001277115.2(DNAH11):c.12387+20T>A AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 31, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001569060.4
Allele description [Variation Report for NM_001277115.2(DNAH11):c.12387+20T>A]
NM_001277115.2(DNAH11):c.12387+20T>A
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 16, 2024