KCNH2 Variant S55W

Summary of observed carriers, functional annotations, and structural context for KCNH2 S55W. Data combine curated literature, international cohorts, and gnomAD observations.

Estimated LQT2 penetrance

29%

2/10 effective observations

Total carriers

0

0 LQT2 · 0 unaffected

Functional studies

0

Publications with functional data

S55W has not been reported in gnomAD. This residue resides in a Hotspot region for LQT2.

We have tested the trafficking efficiency of this variant: 0% of WT with a standard error of 0%. In our analysis we used SE < 20% as 'high quality'. Approximately below 50% of WT is considered PS3 moderate and below 30% is PS3 strong.

Variant features alone are equivalent to phenotyping 2 individuals with LQT2 and 8 unaffected individuals.

In silico predictors

Variant-level computational predictors.
PROVEAN PolyPhen-2 BLAST-PSSM REVEL Penetrance Density LQT2 (%)
-4.185 0.958 -4 0.926 80

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 LQT2 Other Disease
Literature, cohort, and gnomAD 0 0 0
Variant features alone 10 8 2

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. Note that some residues appear multiple times at different distances since the functional KV11.1 channel (protein product of KCNH2/hERG) is a homotetramer and occasionally the same residue from multiple subunits is present within the 15Å window.

Previously observed variants near S55W.
Neighbour residue Distance (Å) Observed variants
55 0 S55L,
58 4 E58K, E58D, E58D,
57 5 A57P,
54 6 Y54X, Y54N,
56 6 R56Q,
49 6 C49G, C49R,
59 6
53 6 G53R, G53S,
857 7 E857X,
44 8 C44W, C44F, C44X,
52 8 C52W,
60 8 M60T,
859 9 T859R, T859M,
48 9
101 9 K101E,
46 10 D46E, D46Y, D46E,
858 10 I858T, I858V,
62 11 R62Q
68 11 F68V, F68L, F68L, F68L,
50 11 E50X,
45 11 N45K, N45D, N45K,
741 11 K741R,
47 11 G47V, G47C,
803 11 D803Y, D803X,
856 12
51 12
804 12
61 12 Q61R,
41 12 V41A,
43 12 Y43C, Y43D,
855 12 S855R, S855R, S855R,
860 12
69 13 L69P, L69Del,
802 13
30 13 I30T, I30Del,
100 13 R100P, R100G, R100Q,
799 13 L799sp,
854 13
66 13 C66Y, C66R, C66G,
102 14 D102X, D102H, D102V,
800 14
42 14 I42N,
861 14 N861I, N861H,
798 14 I798fsX,
740 14 C740G, C740W,
29 14 F29V, F29S, F29L, F29L, F29L,
63 14 P63H,
742 15
797 15 A797T,
28 15 K28E,