KCNQ1 Variant W392R Detail

We estimate the penetrance of LQTS for KCNQ1 W392R is 82%. This variant was found in a total of 7 carriers in 2 papers or gnomAD, 7 had LQTS. W392R is not present in gnomAD. W392R has been functionally characterized in 1 papers. 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 W392R around 82% (13/17).

In Silico Data

PROVEAN PolyPhen-2 BLAST-PSSM REVEL Penetrance Density (%)
-12.22 1.0 0 0.885 79
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
32893267 2020 2 None 2 None
10220144 1999 5 None 5 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.

Functional Data Homozygously Collected

Peak current is relative to wildtype (100% being no different from wildtype). V0.5 activation is the voltages at which half of the maximal current is reached during an activation in units of mV and relative to wildtype. Recovery from inactivation (Rec. inact.) and deactivation time (Deactivation) are the ratio of characteristic time constants with wildtype (unitless).

PubMed ID Cell Type Peak Current IKs (%WT) V1/2 Act. Activation time (%WT) Deactivation time (%WT)
16556865 CHO 0 28.3 None None

Functional Data Heterozygously Collected

Functional parameters are the same as defined above.

PubMed ID Cell Type Peak Current IKs (%WT) V1/2 Act. Activation time (%WT) Deactivation time (%WT)
16556865 CHO None None None

W392R has 31 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
392 0 W392R, W392R, W392ins,
391 5 T391A, T391I,
387 6 P387T,
389 6 S389P,
511 6 R511Q, R511W,
384 6
383 7
514 7 I514T,
518 7 R518Q, R518G,
386 7 N386K, N386K,
393 8 K393N,
390 8
388 8 D388H, D388N,
510 9 H510R, H510Y,
515 9
394 9 I394L,
385 9 E385K,
380 10 R380S, R380S, R380G,
512 10
381 10 C381Y,
508 10 E508G,
513 11 T513A, T513S, T513S,
379 11 W379R, W379R, W379C, W379C, W379G,
382 11
517 12 I517T,
516 12
377 13
378 14 A378T,
509 14 H509Q, H509Q, H509R,
521 14
519 14 R519H, R519C,