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

SCN5A Variant A1932V

Summary of observed carriers, functional annotations, and structural context for SCN5A A1932V. Data combine curated literature, international cohorts, and gnomAD observations.

Estimated LQT3 penetrance

1%

0/21 effective observations

Estimated BrS1 penetrance

3%

0/21 effective observations

Total carriers

11

0 BrS1 · 0 LQT3 · 11 unaffected

A1932V is present in 10 alleles in gnomAD. This residue resides in a Non_Hotspot region for Brugada syndrome and a Non_Hotspot region for LQT3.

Variant features alone are equivalent to phenotyping 0 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 (%)
-1.19 0.001 -1.18 0.249 1 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
15996170 2005 1 0 0 0
Literature, cohort, and gnomAD 11 11 0 0
Variant features alone 15 15 0 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)
15996170 2005

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 A1932V.
Neighbour residue Distance (Å) Observed variants
1917 15
1918 14
1919 14 R1919C, R1919H,
1920 13 S1920C,
1921 13
1922 12 K1922N, K1922R,
1923 11 H1923D, H1923Y,
1924 11 A1924T,
1925 10 p.S1925CfsX20, S1925F,
1926 9
1927 8 L1927P,
1928 8 F1928V,
1929 7 R1929C, R1929H,
1930 5 Q1930H,
1931 4
1932 0 A1932V,
1933 4 G1933A, G1933D, G1933V,
1934 5
1935 7 G1935S,
1936 8
1937 8 S1937A,
1938 9 E1938X, E1938K,
1939 10 p.E1939_E1943del,
1940 11
1941 11
1942 12 P1942H, P1942S
1943 13
1944 13 R1944X, R1944Q,
1945 14
1946 14
1947 15