NM_015040.4(PIKFYVE):c.2095A>G (p.Ile699Val) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 2, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003206152.2
Allele description [Variation Report for NM_015040.4(PIKFYVE):c.2095A>G (p.Ile699Val)]
NM_015040.4(PIKFYVE):c.2095A>G (p.Ile699Val)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
prostaglandin reductase 2 isoform X1 [Macaca mulatta]
prostaglandin reductase 2 isoform X1 [Macaca mulatta]gi|966955726|ref|XP_014999565.1|Protein
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Last Updated: May 1, 2024