NM_001367479.1(DNAH14):c.4985C>T (p.Ala1662Val) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 14, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004231185.1
Allele description [Variation Report for NM_001367479.1(DNAH14):c.4985C>T (p.Ala1662Val)]
NM_001367479.1(DNAH14):c.4985C>T (p.Ala1662Val)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 2, 2024