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SCN5A Variant V1951M

Summary of observed carriers, functional annotations, and structural context for SCN5A V1951M. Data combine curated literature, international cohorts, and gnomAD observations.

Estimated LQT3 penetrance

0%

0/38 effective observations

Estimated BrS1 penetrance

4%

1/38 effective observations

Total carriers

28

1 BrS1 · 0 LQT3 · 27 unaffected

V1951M is present in 27 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 (%)
1.45 0 3.27 0.521 1 5

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
22685113 2012 1 0 0 1 AF
18378609 2008 1 0 0 1 AF
21321465 2011 1 0 1 0
22818067 2012 7 0 0 7 AF
24144883 2014 1 0 0 1 AF
Literature, cohort, and gnomAD 28 27 0 1
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)
22685113 2012 HEK 114 -3.6 0
18378609 2008
21321465 2011
22818067 2012
24144883 2014

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 V1951M.
Neighbour residue Distance (Å) Observed variants
1936 15
1937 14 S1937A,
1938 14 E1938X, E1938K,
1939 13 p.E1939_E1943del,
1940 13
1941 12
1942 11 P1942S, P1942H,
1943 11
1944 10 R1944Q, R1944X,
1945 9
1946 8
1947 8
1948 7 I1948V,
1949 5 A1949S, A1949T,
1950 4 Y1950C,
1951 0 V1951M, V1951L,
1952 4
1953 5 p.S1953RfsX84,
1954 7 E1954K,
1955 8 N1955Y,
1956 8
1957 9 S1957P,
1958 10 R1958Q, R1958P, R1958X,
1959 11
1960 11
1961 12
1962 13 P1962L, P1962S,
1963 13 P1963L,
1964 14 S1964F,
1965 14 S1965N, S1965G,
1966 15