NM_002176.4(IFNB1):c.228C>T (p.Ala76=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Dec 31, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000889992.4
Allele description [Variation Report for NM_002176.4(IFNB1):c.228C>T (p.Ala76=)]
NM_002176.4(IFNB1):c.228C>T (p.Ala76=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Dec 24, 2023