KCNQ1 Variant E261Q Detail

We estimate the penetrance of LQTS for KCNQ1 E261Q is 70%. This variant was found in a total of 1 carriers in 1 papers or gnomAD, 1 had LQTS. E261Q is not present in gnomAD. E261Q has not been functionally characterized. This residue is located in a Hotspot region for LQT1. In silico predictions, functional data (if available), and location in structure are equivalent to observing 6 individuals with LQT1 and 4 unaffected individuals. These data combined with observations of carriers lead us to estimate the LQTS penetrance for KCNQ1 E261Q around 70% (7/11).

In Silico Data

PROVEAN PolyPhen-2 BLAST-PSSM REVEL Penetrance Density (%)
-2.92 0.999 0 0.9 74
PROVEAN scores less than -2 are considered deleterious. REVEL scores higher than 0.5 or 0.75 are considered likely pathogenic (higher sensitivity with the former cutoff, higher specificity with the latter cutoff). A PolyPhen-2 score of 0.85 or greater is considered likely pathogenic. BLAST-PSSM reflects the evolutionary conservation of residue substitutions, more negative numbers indicate fewer observations of the specific substitution than is expected. Penetrance density is our previously published method to calculate the average LQTS probability density in a shell of residues surrounding a residue of interest (Kroncke et al. 2019).

Reported Carrier Data

PubMed ID Year Carriers Unaffected LQT1 Other Disease
19716085 2009 1 None 1 None
Summary totals might not agree with the literature table because of duplicate patients, which were excluded from the total counts. We do not distinguish here between multiple missense codons. Missense variants are combined across degenerate codon substitutions since codon-level data were not consistently available for curation.

E261Q has 19 previously observed neighbors within 15 angstroms

A residue within a folded protein on average has nearest neighbors that fall roughly into two shells: a "nearest" neighbor around 5-6 angstroms and a second shell around 11 angstroms. NOTE: some residues appear multiple times at different distances. This results from the fact that the functional KV7.1 channel is a homotetramer and occasionally the same residue from multiple subunits is present within the 15A window. All variants shown in the rightmost column have been observed in at least one individual in the literature or gnomAD.

Neighbor Distance (Angstroms) Variants Observed in Individuals
247 9 T247I,
254 10 V254M, V254L, V254L,
250 10 L250H, L250P,
251 11 L251P, L251Q,
246 11
255 12
253 12 S253A, S253P,
257 12 I257V,
267 12 Y267C,
252 12 G252R,
248 13 W248C, W248C, W248R, W248R,
269 14 G269D, G269S, G269del,
245 14 G245V,
256 14
242 14 D242N, D242Y,
351 14 F351L, F351L, F351L, F351S,
338 15 S338F,
355 15
339 15 F339del, F339S,