NM_002473.6(MYH9):c.3453G>A (p.Thr1151=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002557096.2
Allele description [Variation Report for NM_002473.6(MYH9):c.3453G>A (p.Thr1151=)]
NM_002473.6(MYH9):c.3453G>A (p.Thr1151=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 16, 2024