NM_001277115.2(DNAH11):c.2824C>A (p.Pro942Thr) AND not provided
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Jul 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000858614.17
Allele description [Variation Report for NM_001277115.2(DNAH11):c.2824C>A (p.Pro942Thr)]
NM_001277115.2(DNAH11):c.2824C>A (p.Pro942Thr)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 8, 2024