NM_022168.4(IFIH1):c.2919G>C (p.Val973=) AND IFIH1-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 30, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003962385.1
Allele description [Variation Report for NM_022168.4(IFIH1):c.2919G>C (p.Val973=)]
NM_022168.4(IFIH1):c.2919G>C (p.Val973=)
Condition(s)
- Name:
- IFIH1-related disorder
- Synonyms:
- IFIH1-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Sep 29, 2024