SCN5A Variant Q379E
Summary of observed carriers, functional annotations, and structural context for SCN5A Q379E. Data combine curated literature, international cohorts, and gnomAD observations.
Estimated LQT3 penetrance
16%
0/10 effective observations
Estimated BrS1 penetrance
36%
3/10 effective observations
Total carriers
0
0 BrS1 · 0 LQT3 · 0 unaffected
Variant features alone are equivalent to phenotyping 3 individuals for Brugada syndrome and 0 individuals for LQT3.
In silico predictors
PROVEAN | PolyPhen-2 | BLAST-PSSM | REVEL | Penetrance Density BrS (%) | Penetrance Density LQT3 (%) |
---|---|---|---|---|---|
NA | NA | NA | 0.881 | 50 | 18 |
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 | 0 | 3 | – | – |
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 |
---|---|---|
333 | 11 | c.998+5G>A, c.998+1G>A, |
364 | 15 | |
1702 | 9 | |
326 | 12 | |
276 | 12 | L276P, L276Q, |
387 | 12 | |
348 | 12 | P348A, |
385 | 12 | A385T, |
355 | 15 | F355C, F355I, |
1715 | 11 | |
1687 | 7 | |
278 | 15 | H278D, H278R, |
372 | 14 | |
388 | 14 | I388S, |
1698 | 13 | A1698T, |
334 | 13 | c.999-424_1338+81del, |
371 | 15 | Q371E, |
1711 | 10 | c.5131delG, |
332 | 11 | A332T, |
1707 | 12 | |
1694 | 14 | |
1704 | 13 | L1704H, |
327 | 13 | |
1706 | 7 | Q1706H, Q1706H, |
1716 | 11 | p.L1716SfsX71, |
376 | 6 | R376H, R376C, |
1714 | 14 | D1714G, |
384 | 10 | S384T, |
1688 | 10 | |
1684 | 13 | W1684R, W1684R, |
354 | 15 | |
329 | 15 | |
1692 | 6 | |
386 | 10 | G386R, G386R, G386E, |
1693 | 11 | |
378 | 5 | |
1699 | 11 | |
331 | 14 | |
349 | 12 | D349N, |
373 | 11 | |
1712 | 10 | G1712C, G1712S, |
379 | 0 | |
1703 | 9 | |
272 | 14 | |
397 | 15 | I397V, I397T, I397F, |
1719 | 14 | |
1709 | 13 | p.T1709del, T1709R, T1709M, |
1701 | 14 | M1701I, M1701I, M1701I, |
325 | 9 | L325R, |
1690 | 12 | D1690N, c.5068_5070delGA, |
392 | 14 | |
324 | 10 | |
389 | 13 | Y389H, Y389X, |
393 | 11 | |
1713 | 14 | |
390 | 12 | |
275 | 15 | N275K, N275K |
383 | 7 | |
1708 | 15 | T1708I, |
323 | 14 | |
382 | 7 | |
374 | 9 | W374G, |
1705 | 11 | |
1689 | 7 | D1689N, |
1700 | 13 | |
367 | 13 | R367C, R367H, R367L, |
381 | 7 | c.1141-3C>A, c.1140+1G>A, |
1686 | 11 | |
375 | 6 | |
1691 | 8 | |
368 | 13 | |
1710 | 14 | S1710L, |
380 | 6 | |
377 | 7 | |
1685 | 14 | |
1419 | 14 | K1419E, |
353 | 13 | T353I, |