SCN5A Variant A413G
Summary of observed carriers, functional annotations, and structural context for SCN5A A413G. Data combine curated literature, international cohorts, and gnomAD observations.
Estimated LQT3 penetrance
41%
2/10 effective observations
Estimated BrS1 penetrance
14%
1/10 effective observations
Total carriers
0
0 BrS1 · 0 LQT3 · 0 unaffected
Variant features alone are equivalent to phenotyping 1 individuals for Brugada syndrome and 2 individuals for LQT3.
In silico predictors
PROVEAN | PolyPhen-2 | BLAST-PSSM | REVEL | Penetrance Density BrS (%) | Penetrance Density LQT3 (%) |
---|---|---|---|---|---|
NA | NA | NA | 0.94 | 10 | 54 |
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
Source | Year | Carriers | Unaffected | LQT3 | BrS1 | Other | Other Disease |
---|---|---|---|---|---|---|---|
Literature, cohort, and gnomAD | – | 0 | 0 | 0 | 0 | – | |
Variant features alone | – | 15 | 12 | 2 | 1 | – | – |
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.
Neighbour residue | Distance (Å) | Observed variants |
---|---|---|
414 | 5 | M414V, |
939 | 8 | L939F, |
404 | 15 | L404V, L404Q, |
937 | 10 | |
1778 | 13 | |
1773 | 11 | |
842 | 14 | |
249 | 10 | K249X, |
943 | 14 | S943N, |
247 | 13 | V247L, V247L, |
240 | 15 | V240M, |
1771 | 12 | I1771T, |
1777 | 13 | V1777L, V1777M, V1777L, |
418 | 9 | E418K, |
926 | 15 | |
250 | 12 | |
409 | 6 | L409P, L409V, |
928 | 12 | L928P, |
417 | 6 | |
934 | 11 | |
933 | 7 | |
1471 | 13 | |
246 | 8 | |
935 | 8 | L935P, |
1779 | 11 | T1779M, |
412 | 4 | V412D, |
1470 | 11 | |
927 | 14 | N927K, N927S, N927K, |
1466 | 12 | c.4396_4397insG, |
245 | 11 | Q245K, |
1776 | 9 | |
244 | 14 | |
1769 | 12 | |
415 | 5 | A415T, |
1768 | 12 | I1768V, |
940 | 9 | S940N, |
1774 | 13 | N1774D, c.5321_5324dupACTT, |
405 | 13 | |
420 | 10 | |
248 | 15 | |
1474 | 14 | |
938 | 11 | |
241 | 12 | |
942 | 14 | |
419 | 11 | Q419X, |
930 | 12 | c.2788-6C>T, c.2787+17_2787+18insACACACACACACACACACACACA, |
1772 | 8 | L1772V, |
239 | 12 | I239V, I239V , |
410 | 5 | A410V, |
1780 | 12 | E1780G, |
242 | 9 | A242D, |
1770 | 15 | I1770V, |
929 | 10 | |
416 | 6 | Y416C, |
413 | 0 | A413T, A413E, |
408 | 9 | |
253 | 14 | |
941 | 13 | S941F, S941N, |
407 | 10 | |
936 | 5 | |
238 | 13 | |
838 | 15 | |
422 | 14 | |
1467 | 12 | |
1775 | 9 | p.F1775LfsX15, F1775V, |
421 | 12 | |
406 | 11 | N406K, N406K, N406S, |
411 | 6 | V411M, |
243 | 11 | |
932 | 8 | |
931 | 12 | |
1646 | 14 | |
1463 | 14 | N1463Y, |