NM_000377.3(WAS):c.991A>T (p.Ile331Phe) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 30, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002563576.2
Allele description [Variation Report for NM_000377.3(WAS):c.991A>T (p.Ile331Phe)]
NM_000377.3(WAS):c.991A>T (p.Ile331Phe)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
S-phase kinase-associated protein 1 [Drosophila sechellia]
S-phase kinase-associated protein 1 [Drosophila sechellia]gi|1818137375|ref|XP_032575337.1|Protein
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024