NM_005142.3(CBLIF):c.220C>T (p.Leu74Phe) AND Hereditary intrinsic factor deficiency
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 28, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003005030.3
Allele description [Variation Report for NM_005142.3(CBLIF):c.220C>T (p.Leu74Phe)]
NM_005142.3(CBLIF):c.220C>T (p.Leu74Phe)
Condition(s)
-
Homo sapiens cDNA, FLJ94625, Homo sapiens related RAS viral (r-ras) oncogene hom...
Homo sapiens cDNA, FLJ94625, Homo sapiens related RAS viral (r-ras) oncogene homolog 2 (RRAS2),mRNAgi|164696353|dbj|AK313976.1|Nucleotide
-
Homo sapiens actin filament associated protein 1 like 1 (AFAP1L1), transcript va...
Homo sapiens actin filament associated protein 1 like 1 (AFAP1L1), transcript variant 1, mRNAgi|1519311705|ref|NM_152406.4|Nucleotide
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Last Updated: Sep 29, 2024