NM_000260.4(MYO7A):c.1997G>A (p.Arg666Gln) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 13, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001309116.2
Allele description [Variation Report for NM_000260.4(MYO7A):c.1997G>A (p.Arg666Gln)]
NM_000260.4(MYO7A):c.1997G>A (p.Arg666Gln)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 6, 2024