NM_022168.4(IFIH1):c.2858A>G (p.Asp953Gly) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 18, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004629552.1
Allele description [Variation Report for NM_022168.4(IFIH1):c.2858A>G (p.Asp953Gly)]
NM_022168.4(IFIH1):c.2858A>G (p.Asp953Gly)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Oct 13, 2024