NM_000202.8(IDS):c.642G>A (p.Thr214=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 30, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002368496.2
Allele description [Variation Report for NM_000202.8(IDS):c.642G>A (p.Thr214=)]
NM_000202.8(IDS):c.642G>A (p.Thr214=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Sep 29, 2024