NM_005477.3(HCN4):c.2538G>A (p.Pro846=) AND Brugada syndrome 8
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 20, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001430008.6
Allele description [Variation Report for NM_005477.3(HCN4):c.2538G>A (p.Pro846=)]
NM_005477.3(HCN4):c.2538G>A (p.Pro846=)
Condition(s)
-
M23253 (0)
GEO Profiles
-
suppression of tumorigenicity 18 protein isoform e [Homo sapiens]
suppression of tumorigenicity 18 protein isoform e [Homo sapiens]gi|1209857063|ref|NP_001339806.1|Protein
-
PREDICTED: Rattus norvegicus F-box and WD repeat domain containing 4 (Fbxw4), tr...
PREDICTED: Rattus norvegicus F-box and WD repeat domain containing 4 (Fbxw4), transcript variant X4, mRNAgi|2678867616|ref|XM_063264895.1|Nucleotide
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Last Updated: May 1, 2024