NM_015338.6(ASXL1):c.3914T>G (p.Phe1305Cys) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 15, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002724160.2
Allele description [Variation Report for NM_015338.6(ASXL1):c.3914T>G (p.Phe1305Cys)]
NM_015338.6(ASXL1):c.3914T>G (p.Phe1305Cys)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
DUF2771 domain-containing protein [Corynebacterium pseudotuberculosis]
DUF2771 domain-containing protein [Corynebacterium pseudotuberculosis]gi|503006478|ref|WP_013241454.1|Protein
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Last Updated: May 1, 2024