NM_000901.5(NR3C2):c.1092G>A (p.Thr364=) AND Autosomal dominant pseudohypoaldosteronism type 1
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000312831.5
Allele description [Variation Report for NM_000901.5(NR3C2):c.1092G>A (p.Thr364=)]
NM_000901.5(NR3C2):c.1092G>A (p.Thr364=)
Condition(s)
-
FBXW7 F-box and WD repeat domain containing 7 [Homo sapiens]
FBXW7 F-box and WD repeat domain containing 7 [Homo sapiens]Gene ID:55294Gene
-
Gene Links for GEO Profiles (Select 100898105) (1)
Gene
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Last Updated: Oct 13, 2024