NM_000260.4(MYO7A):c.1477C>G (p.Gln493Glu) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 12, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002620460.1
Allele description [Variation Report for NM_000260.4(MYO7A):c.1477C>G (p.Gln493Glu)]
NM_000260.4(MYO7A):c.1477C>G (p.Gln493Glu)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Feb 13, 2023