NM_139058.3(ARX):c.306GGC[9] (p.Ala115del) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 17, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002313230.9
Allele description [Variation Report for NM_139058.3(ARX):c.306GGC[9] (p.Ala115del)]
NM_139058.3(ARX):c.306GGC[9] (p.Ala115del)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
CHST5 carbohydrate sulfotransferase 5 [Homo sapiens]
CHST5 carbohydrate sulfotransferase 5 [Homo sapiens]Gene ID:23563Gene
-
Gene Links for GEO Profiles (Select 114679188) (1)
Gene
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Last Updated: Sep 1, 2024