KCNQ1 Variant V215M

Summary of observed carriers, functional annotations, and structural context for KCNQ1 V215M. Data combine curated literature, international cohorts, and gnomAD observations.

Estimated LQT1 penetrance

44%

6/15 effective observations

Total carriers

5

2 LQT1 · 3 unaffected

Functional studies

1

Publications with functional data

V215M is present in 3 alleles in gnomAD. This residue resides in a Hotspot region for LQT1.

Variant features alone are equivalent to phenotyping 4 individuals with LQT1 and 6 unaffected individuals.

In silico predictors

Variant-level computational predictors.
PROVEAN PolyPhen-2 BLAST-PSSM REVEL Penetrance Density LQT1 (%)
-1.28 0.991 1 0.811 48

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
32893267 2020 1 None 1 None
26715165 2016 1 None 1 None
22949429 2012 1 None 1 None
20421371 2010 None None None None
19841300 2009 1 None 1 None
19716085 2009 1 None 1 None
Literature, cohort, and gnomAD 5 3 2
Variant features alone 15 6 4

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

Functional data

Functional assay results from published electrophysiology studies. HM indicates homomeric channels, HT indicates heteromeric channels.

Homomeric channel data

Published electrophysiology measurements (homomeric).
PubMed ID Year Study Type Assay Temperature Cell Type Result

Heteromeric channel data

Published electrophysiology measurements (heteromeric).
PubMed ID Year Study Type Assay Temperature Cell Type Result

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 V215M.
Neighbour residue Distance (Å) Observed variants
215 0 V215M, V215G, V215L, V215L
216 4 G216R,
214 5 C214Y,
219 5 G219E,
221 5
212 6
222 6
211 7
213 7
217 7
218 7
220 8 Q220K,
226 8 A226V,
223 9
225 9 S225L, S225del,
210 9 M210I, M210I, M210I,
224 10 T224M,
209 10 S209P,
157 11 F157C,
208 11 A208V,
227 11
230 12
161 12
229 13 G229D,
207 13 V207M, V207L, V207L, V207L, V207L, V207del,
160 13 E160del, E160K, E160V,
228 14
164 14
153 14 T153M,
233 15 L233P,
206 15 V206L,