SCN5A Variant K126T

Summary of observed carriers, functional annotations, and structural context for SCN5A K126T. Data combine curated literature, international cohorts, and gnomAD observations.

Estimated LQT3 penetrance

4%

0/10 effective observations

Estimated BrS1 penetrance

49%

4/10 effective observations

Total carriers

0

0 BrS1 · 0 LQT3 · 0 unaffected

K126T has not been reported in gnomAD. This residue resides in a Hotspot region for Brugada syndrome and a Non_Hotspot region for LQT3.

Variant features alone are equivalent to phenotyping 4 individuals for Brugada syndrome and 0 individuals for LQT3.

In silico predictors

Variant-level computational predictors.
PROVEAN PolyPhen-2 BLAST-PSSM REVEL Penetrance Density BrS (%) Penetrance Density LQT3 (%)
NA NA NA 0.851 74 1

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. Penetrance density summarises neighbouring residue risk (Kroncke et al. 2019).

Reported carrier data

Observed carriers by publication or cohort.
Source Year Carriers Unaffected LQT3 BrS1 Other Other Disease
Literature, cohort, and gnomAD – 0 0 0 0 –
Variant features alone – 15 11 0 4 – –

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 K126T.
Neighbour residue Distance (Å) Observed variants
126 0 K126E,
175 13 K175N, K175N,
129 7
178 10 A178G,
128 8 c.381dupT,
117 14
119 10 P119S, P119L,
179 12 R179X, R179Q
177 12 L177P,
123 4 A123G, A123V,
121 9 R121W, R121Q,
127 6
124 6 A124D,
118 13
125 5 V125L, V125L,
131 12
174 11 V174I,
133 11
115 14 S115G,
173 15
132 13 c.393-5C>A,
114 15
130 8
170 14 F170I,
116 12
134 13 N134S,
120 10
122 7