NM_016239.4(MYO15A):c.2418C>T (p.Phe806=) AND not specified
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Oct 17, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000218897.8
Allele description [Variation Report for NM_016239.4(MYO15A):c.2418C>T (p.Phe806=)]
NM_016239.4(MYO15A):c.2418C>T (p.Phe806=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 20, 2024