NM_001369.3(DNAH5):c.11385G>A (p.Val3795=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 9, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000937281.3
Allele description
NM_001369.3(DNAH5):c.11385G>A (p.Val3795=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Feb 13, 2023