NM_004998.4(MYO1E):c.1747T>C (p.Tyr583His) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 14, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001318700.6
Allele description [Variation Report for NM_004998.4(MYO1E):c.1747T>C (p.Tyr583His)]
NM_004998.4(MYO1E):c.1747T>C (p.Tyr583His)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024