NM_016239.4(MYO15A):c.6743C>T (p.Ala2248Val) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Mar 2, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000038979.6
Allele description [Variation Report for NM_016239.4(MYO15A):c.6743C>T (p.Ala2248Val)]
NM_016239.4(MYO15A):c.6743C>T (p.Ala2248Val)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 28, 2024