KCNH2 Variant P63H

Summary of observed carriers, functional annotations, and structural context for KCNH2 P63H. Data combine curated literature, international cohorts, and gnomAD observations.

Estimated LQT2 penetrance

17%

90% CI: 3.1% – 37.8%

1/11 effective observations

Total carriers

1

0 LQT2 · 1 unaffected

Functional studies

0

Publications with functional data

P63H is present in 1 alleles in gnomAD. This residue resides in a Hotspot region for LQT2.

We have tested the trafficking efficiency of this variant: 42% of WT with a standard error of 14%. 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 1 individuals with LQT2 and 9 unaffected individuals.

In silico predictors

Variant-level computational predictors.
PROVEAN PolyPhen-2 BLAST-PSSM REVEL Penetrance Density LQT2 (%)
-6.033 1.0 -3 0.806 41

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 – 1 1 0 –
Variant features alone – 10 9 1 –

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 P63H.
Neighbour residue Distance (Å) Observed variants
63 0 P63H,
64 5 C64R, C64Y,
62 5 R62Q,
65 5 T65P,
66 6 C66R, C66G, C66Y,
40 6
38 6
39 6 C39R, C39X,
41 7 V41A,
67 7
68 8 F68L, F68V, F68L, F68L,
59 9
61 9 Q61R,
32 9 A32T,
60 10 M60T,
36 10 V36X,
69 10 L69Del, L69P,
37 11
30 11 I30Del, I30T,
42 11 I42N,
33 11 N33T
70 11 H70R, H70Q, H70Q,
86 11 L86R,
83 11 A83P, A83fsX,
125 11
82 12 I82Del, I82dup, I82Ins, I82T,
127 12
31 12 I31S,
58 12 E58K, E58D, E58D,
34 12 A34T,
796 12 V796L, V796L, V796Del,
57 13 A57P,
54 13 Y54N, Y54X,
79 13 A79T, A79S, A79Del, A79fsX,
44 13 C44F, C44X, C44W,
48 14
35 14 R35W,
98 14
124 14 M124T, M124R,
85 14 A85P, A85V,
87 14 L87P,
55 14 S55L,
797 14 A797T,
80 15 A80P,
43 15 Y43D, Y43C,
52 15 C52W,
126 15
860 15
56 15 R56Q,
112 15 V112M,
795 15 V795I,