NM_005249.5(FOXG1):c.1399C>T (p.Leu467=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 26, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002390492.2
Allele description [Variation Report for NM_005249.5(FOXG1):c.1399C>T (p.Leu467=)]
NM_005249.5(FOXG1):c.1399C>T (p.Leu467=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
sialate:O-sulfotransferase 1 isoform 3 [Homo sapiens]
sialate:O-sulfotransferase 1 isoform 3 [Homo sapiens]gi|1924573859|ref|NP_001375340.1|Protein
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Last Updated: Sep 29, 2024