Update Variant Browser refresh
Explore redesigned navigation and faster access to curated variant datasets.

SCN5A Variant R1919C

Summary of observed carriers, functional annotations, and structural context for SCN5A R1919C. Data combine curated literature, international cohorts, and gnomAD observations.

Estimated LQT3 penetrance

2%

0/17 effective observations

Estimated BrS1 penetrance

9%

1/17 effective observations

Total carriers

7

0 BrS1 · 0 LQT3 · 7 unaffected

R1919C is present in 6 alleles in gnomAD. This residue resides in a Mild_Hotspot region for Brugada syndrome and a Non_Hotspot region for LQT3.

Variant features alone are equivalent to phenotyping 1 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 (%)
-5.43 0.893 -1.23 0.802 13 0

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
20129283 2010 1 0 0 0
29325976 2018 1 0 1 0
Literature, cohort, and gnomAD 7 7 0 0
Variant features alone 15 14 0 1

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)
20129283 2010
29325976 2018

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 R1919C.
Neighbour residue Distance (Å) Observed variants
1904 15 S1904L,
1905 14
1906 14 M1906V, M1906T,
1907 13
1908 13 I1908V,
1909 12 Q1909R,
1910 11 R1910K,
1911 11
1912 10
1913 9 R1913C, R1913H, R1913S,
1914 8 R1914G,
1915 8 H1915P, H1915Y, H1915Q, H1915N,
1916 7
1917 5
1918 4
1919 0 R1919H, R1919C
1920 4 S1920C,
1921 5
1922 7 K1922N, K1922R,
1923 8 H1923D, H1923Y,
1924 8 A1924T,
1925 9 p.S1925CfsX20, S1925F,
1926 10
1927 11 L1927P,
1928 11 F1928V,
1929 12 R1929H, R1929C,
1930 13 Q1930H,
1931 13
1932 14 A1932V,
1933 14 G1933D, G1933A, G1933V,
1934 15