S37N (p.Ser37Asn) variant of KCNE1 (P15382)
S37N (p.Ser37Asn) in KCNE1 (P15382) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Long QT syndrome. The available variant effect predictions contribute to a CATVariant prioritization score of 0.35 / 1. The record also includes experimental measurements, published literature, and structural context.
S37N (p.Ser37Asn) variant details
- p.Ser37Asn
- rs1290531137
- ClinGen CA410198465
- cosmic curated COSV61606
- ClinVar RCV000823043
- Uncertain significance
- Long QT syndrome
- Missense
- Variant Prioritization Score for Impact Estimate 0.352
- ESM-1b 0.00
- AlphaMissense 0.07
- MetaLR 0.47
- MetaSVM -0.32
- MutPred 0.15
- ClinVar: Uncertain significance (Long QT syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available
- Trafficking scores for KCNE1 in the presence of KCNQ1: score 1.26
- Cited in: Long QT Syndrome Overview. (PMID 20301308)
- Cited in: Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited… (PMID 23994779)