NM_006790.3(MYOT):c.1401T>C (p.Asn467=) AND not provided
- Germline classification:
- Conflicting interpretations of pathogenicity (5 submissions)
- Last evaluated:
- Nov 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000726159.30
Allele description [Variation Report for NM_006790.3(MYOT):c.1401T>C (p.Asn467=)]
NM_006790.3(MYOT):c.1401T>C (p.Asn467=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 20, 2024