NM_001277115.2(DNAH11):c.10472G>A (p.Arg3491His) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 23, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000218296.10
Allele description [Variation Report for NM_001277115.2(DNAH11):c.10472G>A (p.Arg3491His)]
NM_001277115.2(DNAH11):c.10472G>A (p.Arg3491His)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 1, 2024