NM_001369.3(DNAH5):c.13753C>A (p.Pro4585Thr) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 7, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000734674.4
Allele description [Variation Report for NM_001369.3(DNAH5):c.13753C>A (p.Pro4585Thr)]
NM_001369.3(DNAH5):c.13753C>A (p.Pro4585Thr)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Apr 1, 2023