NM_016239.4(MYO15A):c.7473+10G>T AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 30, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000215201.5
Allele description [Variation Report for NM_016239.4(MYO15A):c.7473+10G>T]
NM_016239.4(MYO15A):c.7473+10G>T
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024