NM_000260.4(MYO7A):c.3193A>G (p.Ser1065Gly) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 1, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001321780.5
Allele description [Variation Report for NM_000260.4(MYO7A):c.3193A>G (p.Ser1065Gly)]
NM_000260.4(MYO7A):c.3193A>G (p.Ser1065Gly)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Aug 13, 2023