NM_006790.3(MYOT):c.1275A>G (p.Ala425=) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jun 26, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000363482.5
Allele description [Variation Report for NM_006790.3(MYOT):c.1275A>G (p.Ala425=)]
NM_006790.3(MYOT):c.1275A>G (p.Ala425=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024