KCNQ1 Variant A352T

Summary of observed carriers, functional annotations, and structural context for KCNQ1 A352T. Data combine curated literature, international cohorts, and gnomAD observations.

Estimated LQT1 penetrance

79%

7/10 effective observations

Total carriers

0

0 LQT1 · 0 unaffected

Functional studies

0

Publications with functional data

A352T has not been reported in gnomAD. This residue resides in a Hotspot region for LQT1.

Variant features alone are equivalent to phenotyping 7 individuals with LQT1 and 3 unaffected individuals.

In silico predictors

Variant-level computational predictors.
PROVEAN PolyPhen-2 BLAST-PSSM REVEL Penetrance Density LQT1 (%)
-3.67 0.995 -1 0.922 87

PROVEAN scores below -2 suggest deleterious impact. REVEL scores above 0.5–0.75 are often interpreted as likely pathogenic. PolyPhen-2 scores above 0.85 are typically pathogenic. BLAST-PSSM reflects evolutionary conservation; more negative values indicate rarer substitutions. Penetrance density summarises neighbouring residue risk (Kroncke et al. 2019).

Reported carrier data

Observed carriers by publication or cohort.
Source Year Carriers Unaffected LQT1 Other Disease
Literature, cohort, and gnomAD 0 0 0
Variant features alone 15 3 7

Totals may differ from individual publications due to duplicate patients removed during curation.

Nearby variants

Neighbouring residues within 15 Ångström provide structural context. Variants listed in the right-most column have been observed clinically or in gnomAD.

Previously observed variants near A352T.
Neighbour residue Distance (Å) Observed variants
349 9 S349W,
352 9
353 10 L353P,
350 10 G350V, G350R, G350R, G350W,
348 11
345 12 G345R, G345R, G345A,
346 12
356 12
351 13 F351L, F351L, F351L, F351S,
355 13
347 13 L347P, L347R,
253 14 S253A, S253P
258 14 H258P, H258N, H258R, H258Y,
344 14 A344V, A344E,
357 14 Q357H, Q357H,
354 14
260 15
256 15
255 15
252 15 G252R,