NM_000261.2(MYOC):c.39T>G (p.Pro13=) AND not provided
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Jan 22, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000946527.8
Allele description [Variation Report for NM_000261.2(MYOC):c.39T>G (p.Pro13=)]
NM_000261.2(MYOC):c.39T>G (p.Pro13=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024