SCN5A Variant Q1414H
Summary of observed carriers, functional annotations, and structural context for SCN5A Q1414H. Data combine curated literature, international cohorts, and gnomAD observations.
Estimated LQT3 penetrance
16%
0/11 effective observations
Estimated BrS1 penetrance
25%
2/11 effective observations
Total carriers
1
0 BrS1 · 0 LQT3 · 1 unaffected
Variant features alone are equivalent to phenotyping 2 individuals for Brugada syndrome and 0 individuals for LQT3.
In silico predictors
PROVEAN | PolyPhen-2 | BLAST-PSSM | REVEL | Penetrance Density BrS (%) | Penetrance Density LQT3 (%) |
---|---|---|---|---|---|
-4.87 | 1 | -3.53 | 0.902 | 35 | 26 |
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 | – | 1 | 1 | 0 | 0 | – | |
Variant features alone | – | 15 | 13 | 0 | 2 | – | – |
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 |
---|---|---|
896 | 13 | C896S, C896S, |
1417 | 6 | |
1406 | 12 | G1406E, G1406R, G1406R, |
1457 | 13 | |
1453 | 11 | |
1757 | 14 | |
1715 | 10 | |
1449 | 14 | Y1449C, Y1449S, |
1756 | 10 | I1756V, |
1711 | 11 | c.5131delG, |
1450 | 12 | |
1754 | 15 | |
1707 | 12 | |
1398 | 13 | V1398M, |
1411 | 5 | |
1407 | 10 | |
1458 | 12 | S1458Y, |
1410 | 7 | |
1706 | 15 | Q1706H, Q1706H, |
1716 | 11 | p.L1716SfsX71, |
1714 | 6 | D1714G, |
897 | 14 | G897E, G897R, G897R, |
1348 | 14 | F1348L, F1348L, F1348L, |
1404 | 15 | |
1423 | 10 | D1423H, |
1721 | 13 | |
1349 | 14 | |
1753 | 11 | T1753A, |
1422 | 10 | M1422R, |
1418 | 8 | |
373 | 14 | |
1712 | 9 | G1712C, G1712S, |
1341 | 15 | |
1356 | 15 | c.4066_4068delTT, |
898 | 13 | |
893 | 14 | R893H, R893C, |
1462 | 12 | |
1412 | 7 | L1412F, |
1719 | 14 | |
1408 | 9 | G1408R, G1408R, |
1709 | 14 | p.T1709del, T1709R, T1709M, |
1420 | 6 | G1420R, G1420V, G1420P, G1420D, |
1360 | 14 | F1360C, |
1755 | 14 | |
1401 | 11 | |
1425 | 12 | |
1399 | 12 | |
1713 | 7 | |
1454 | 12 | |
1427 | 14 | A1427E, A1427S, |
1424 | 8 | I1424V, |
1748 | 13 | p.G1748del, G1748D, |
1405 | 14 | V1405L, V1405L, V1405M, |
1409 | 9 | Y1409C, Y1409X, |
1400 | 8 | V1400I, |
1421 | 8 | |
1718 | 11 | S1718R, S1718R, S1718R, |
1345 | 11 | W1345C, W1345C, |
1717 | 9 | L1717P, |
1751 | 15 | |
1416 | 7 | c.4245+2T>A, A1416G, A1416E, c.4245+1G>A, c.4245+1G>C, |
1760 | 12 | |
1752 | 11 | |
1686 | 14 | |
1761 | 13 | L1761F, L1761H, c.5280delG, |
1749 | 12 | I1749N, |
375 | 14 | |
1710 | 9 | S1710L, |
1720 | 14 | c.5157delC, |
1415 | 5 | |
1428 | 14 | A1428V, A1428S, |
1419 | 6 | K1419E, |
1414 | 0 | Q1414H, Q1414H, |
1402 | 11 | |
1413 | 5 |