NM_016239.4(MYO15A):c.3012A>G (p.Ser1004=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 13, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000613260.4
Allele description [Variation Report for NM_016239.4(MYO15A):c.3012A>G (p.Ser1004=)]
NM_016239.4(MYO15A):c.3012A>G (p.Ser1004=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024