NM_005142.3(CBLIF):c.59C>T (p.Thr20Ile) AND Hereditary intrinsic factor deficiency
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Dec 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000949346.7
Allele description [Variation Report for NM_005142.3(CBLIF):c.59C>T (p.Thr20Ile)]
NM_005142.3(CBLIF):c.59C>T (p.Thr20Ile)
Condition(s)
Assertion and evidence details
Last Updated: Mar 16, 2024