NM_000071.3(CBS):c.1059G>A (p.Thr353=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 5, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001812186.13
Allele description [Variation Report for NM_000071.3(CBS):c.1059G>A (p.Thr353=)]
NM_000071.3(CBS):c.1059G>A (p.Thr353=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 13, 2024