SCN5A Variant P1021S

Summary of observed carriers, functional annotations, and structural context for SCN5A P1021S. Data combine curated literature, international cohorts, and gnomAD observations.

Estimated LQT3 penetrance

48%

6/18 effective observations

Estimated BrS1 penetrance

5%

0/18 effective observations

Total carriers

8

0 BrS1 · 5 LQT3 · 3 unaffected

P1021S is present in 3 alleles in gnomAD. This residue resides in a Non_Hotspot region for Brugada syndrome and a Mild_Hotspot region for LQT3.

Variant features alone are equivalent to phenotyping 0 individuals for Brugada syndrome and 1 individuals for LQT3.

In silico predictors

Variant-level computational predictors.
PROVEAN PolyPhen-2 BLAST-PSSM REVEL Penetrance Density BrS (%) Penetrance Density LQT3 (%)
0.38 0.43 -0.12 0.524 3 37

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
27566755 2016 5 5 0 0
Literature, cohort, and gnomAD 8 3 5 0
Variant features alone 15 14 1 0

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

Functional data

Peak and late/persistent current values are relative to wild-type (100% indicates no change). V1/2 activation and inactivation denote the membrane potentials (mV) at which half-maximal current is achieved.

Published electrophysiology measurements.
PubMed ID Year Cell Type Peak Current (% WT) V1/2 Activation (mV) V1/2 Inactivation (mV) Late/Persistent Current (% WT)
27566755 2016

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 P1021S.
Neighbour residue Distance (Å) Observed variants
1006 15 A1006S,
1007 14 T1007N, T1007I,
1008 14 P1008S,
1009 13
1010 13
1011 12 P1011L, P1011S,
1012 11
1013 11
1014 10 P1014S,
1015 9 p.G1015DfsX14, E1015K,
1016 8 c.3045_3046delGA, T1016M,
1017 8
1018 7 K1018E,
1019 5
1020 4
1021 0 P1021S,
1022 4
1023 5 R1023H, R1023P, R1023C,
1024 7 K1024R,
1025 8 E1025A,
1026 8
1027 9 R1027P, R1027Q, R1027W,
1028 10
1029 11 E1029K,
1030 11
1031 12 p.G1031fsX27,
1032 13 E1032D, E1032D, E1032K,
1033 13 Q1033R,
1034 14 P1034T,
1035 14 G1035V,
1036 15