NM_016239.4(MYO15A):c.4954C>T (p.Leu1652=) AND not specified
- Germline classification:
- Benign (5 submissions)
- Last evaluated:
- May 9, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000217929.14
Allele description [Variation Report for NM_016239.4(MYO15A):c.4954C>T (p.Leu1652=)]
NM_016239.4(MYO15A):c.4954C>T (p.Leu1652=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024