SCN5A Variant c.5290delG

Summary of observed carriers, functional annotations, and structural context for SCN5A c.5290delG. Data combine curated literature, international cohorts, and gnomAD observations.

Estimated LQT3 penetrance

22%

1/11 effective observations

Estimated BrS1 penetrance

46%

5/11 effective observations

Total carriers

1

1 BrS1 · 0 LQT3 · 0 unaffected

c.5290delG has not been reported in gnomAD. This residue resides in a Hotspot region for Brugada syndrome and a Mild_Hotspot region for LQT3.

Variant features alone are equivalent to phenotyping 4 individuals for Brugada syndrome and 1 individuals for LQT3.

In silico predictors

Variant-level computational predictors.
PROVEAN PolyPhen-2 BLAST-PSSM REVEL Penetrance Density BrS (%) Penetrance Density LQT3 (%)
NA NA NA None 58 33

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
17697823 2007 1 0 1 0
28341781 2017 1 0 1 0
20129283 2010 1 0 1 0
Literature, cohort, and gnomAD 1 0 0 1
Variant features alone 15 10 1 4

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)
17697823 2007
28341781 2017
20129283 2010

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 c.5290delG.
Neighbour residue Distance (Å) Observed variants
403 11
1659 13
404 14 L404Q, L404V,
1417 13
1765 4
1653 14
1757 11
1472 15 N1472S, p.N1472del,
1771 11 I1771T,
401 10 S401P,
1756 11 I1756V,
1320 15 M1320I, M1320I, M1320I,
1764 0 c.5290delG, V1764F,
1666 15
371 11 Q371E,
409 13 L409P, L409V,
1711 13 c.5131delG,
1754 14
1707 12
1656 13
1704 13 L1704H,
1706 14 Q1706H, Q1706H,
1671 15
935 14 L935P,
1762 7 I1762M, p.I1762del,
1470 12
1464 14 L1464P, c.4389_4396delCCTCTTTA,
1668 12 M1668T,
1466 9 c.4396_4397insG,
369 15 M369K,
1767 6 Y1767C,
1660 8 I1660V, I1660S,
1769 9
402 7 F402L, F402L, F402L,
1766 6 M1766T, M1766L, M1766V, M1766L,
1665 14
1768 7 I1768V,
1473 12 F1473S, F1473C,
1334 14 I1334V,
1468 13 V1468F, V1468A,
1663 10
399 14
397 11 I397F, I397T, I397V,
405 11
1462 12
1657 10
1759 6 S1759C,
1662 13
1324 15
1327 12
1709 8 p.T1709del, T1709M, T1709R,
1758 9 I1758V, p.I1758del,
1755 10
1330 14 A1330D, A1330T, A1330P,
1772 13 L1772V,
1713 13
1323 12 V1323G,
394 14
1770 11 I1770V,
1708 8 T1708I,
374 14 W374G,
1705 13
1326 13 A1326S,
1763 4 V1763M, V1763L, V1763L,
1465 11 p.F1465_L1480dup,
1760 6
1467 13
370 14 T370M,
1661 10 G1661R, G1661R, G1661E,
1761 8 L1761F, L1761H, c.5280delG,
1469 10 I1469V,
406 10 N406S, N406K, N406K,
1710 10 S1710L,
932 15
398 10
400 13 G400R, G400A, G400R, G400E,
1667 12 V1667I,
1664 8
1463 12 N1463Y,
1658 14