NM_015175.3(NBEAL2):c.4217G>T (p.Ser1406Ile) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 5, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004467506.1
Allele description [Variation Report for NM_015175.3(NBEAL2):c.4217G>T (p.Ser1406Ile)]
NM_015175.3(NBEAL2):c.4217G>T (p.Ser1406Ile)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Mus musculus casein kinase 1, gamma 2 (Csnk1g2), transcript variant 2, mRNA
Mus musculus casein kinase 1, gamma 2 (Csnk1g2), transcript variant 2, mRNAgi|227430312|ref|NM_001159591.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 7, 2024