KCNH2 Variant F68L

Summary of observed carriers, functional annotations, and structural context for KCNH2 F68L. Data combine curated literature, international cohorts, and gnomAD observations.

Estimated LQT2 penetrance

41%

8/15 effective observations

Total carriers

5

5 LQT2 · 0 unaffected

Functional studies

0

Publications with functional data

F68L 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 10%. 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 3 individuals with LQT2 and 7 unaffected individuals.

In silico predictors

Variant-level computational predictors.
PROVEAN PolyPhen-2 BLAST-PSSM REVEL Penetrance Density LQT2 (%)
-4.031 0.999 0 0.894 81

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
Japan Cohort 2020 4 0 4
21063070 2010 1 0 1
Literature, cohort, and gnomAD 5 0 5
Variant features alone 10 7 3

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 F68L.
Neighbour residue Distance (Å) Observed variants
68 0 F68L, F68V, F68L, F68L,
69 4 L69Del, L69P,
66 5 C66R, C66G, C66Y,
67 5
54 7 Y54N, Y54X,
70 7 H70R, H70Q, H70Q,
62 7 R62Q,
59 8
63 8 P63H,
58 8 E58K, E58D, E58D,
52 8 C52W,
65 9 T65P,
98 9
101 9 K101E,
99 10 Y99N, Y99S,
71 10 G71R, G71R, G71W, G71E,
53 10 G53S, G53R,
64 10 C64R, C64Y,
48 11
55 11 S55L,
100 11 R100G, R100Q, R100P,
41 11 V41A,
57 12 A57P,
60 12 M60T,
51 12
49 12 C49R, C49G,
30 12 I30Del, I30T
103 12
74 12 T74fsX, T74M,
106 12 F106L, F106V, F106L, F106L,
97 12
61 13 Q61R,
102 13 D102H, D102V, D102X,
96 13 I96V, I96T,
40 13
44 13 C44F, C44X, C44W,
72 13 P72T, P72S, P72Q, P72R,
129 13 F129C,
79 13 A79T, A79S, A79Del, A79fsX,
104 13
105 14
127 14
82 14 I82Del, I82dup, I82Ins, I82T,
56 14 R56Q,
39 14 C39R, C39X,
38 14
108 14 C108Y,
73 14 R73G, R73C, R73fsX, R73H,
110 15 V110A,