NM_005097.4(LGI1):c.812C>T (p.Thr271Ile) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 31, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002415810.9
Allele description [Variation Report for NM_005097.4(LGI1):c.812C>T (p.Thr271Ile)]
NM_005097.4(LGI1):c.812C>T (p.Thr271Ile)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Ribosomal protein L19 family protein [Arabidopsis thaliana]
Ribosomal protein L19 family protein [Arabidopsis thaliana]gi|15239778|ref|NP_196736.1|Protein
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Last Updated: Oct 20, 2024