NM_003680.4(YARS1):c.1275C>T (p.Asn425=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 11, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002461061.2
Allele description [Variation Report for NM_003680.4(YARS1):c.1275C>T (p.Asn425=)]
NM_003680.4(YARS1):c.1275C>T (p.Asn425=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Phospho2 protein [synthetic construct]
Phospho2 protein [synthetic construct]gi|19343650|gb|AAH25612.1|Protein
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Last Updated: Sep 29, 2024