NM_000202.8(IDS):c.445T>G (p.Ser149Ala) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 4, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002332544.3
Allele description [Variation Report for NM_000202.8(IDS):c.445T>G (p.Ser149Ala)]
NM_000202.8(IDS):c.445T>G (p.Ser149Ala)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Homo sapiens Ras protein specific guanine nucleotide releasing factor 1 (RASGRF1...
Homo sapiens Ras protein specific guanine nucleotide releasing factor 1 (RASGRF1), transcript variant 1, mRNAgi|224586878|ref|NM_002891.4|Nucleotide
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Last Updated: Oct 8, 2024