NM_015836.4(WARS2):c.791A>G (p.Tyr264Cys) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 24, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002517424.2
Allele description [Variation Report for NM_015836.4(WARS2):c.791A>G (p.Tyr264Cys)]
NM_015836.4(WARS2):c.791A>G (p.Tyr264Cys)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Mus musculus RIKEN cDNA 2810433K01 gene (2810433K01Rik), mRNA
Mus musculus RIKEN cDNA 2810433K01 gene (2810433K01Rik), mRNAgi|142367006|ref|NM_025581.3|Nucleotide
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Last Updated: Sep 29, 2024