SCN5A Variant c.3667delG

Summary of observed carriers, functional annotations, and structural context for SCN5A c.3667delG. Data combine curated literature, international cohorts, and gnomAD observations.

Estimated LQT3 penetrance

10%

1/15 effective observations

Estimated BrS1 penetrance

41%

6/15 effective observations

Total carriers

5

3 BrS1 · 0 LQT3 · 2 unaffected

c.3667delG 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 3 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 41 25

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
17404158 2007 1 0 1 0
20031634 2009 5 0 3 0
26921764 2016 1 0 1 0
20129283 2010 1 0 1 0
Literature, cohort, and gnomAD 5 2 0 3
Variant features alone 15 11 1 3

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)
17404158 2007
20031634 2009
26921764 2016
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.3667delG.
Neighbour residue Distance (Å) Observed variants
1702 14
387 15
1218 9 S1218T, S1218I,
1304 11 T1304M,
1217 11
1243 15 D1243N,
1216 11 L1216V,
1234 15
1698 9 A1698T,
1220 5 G1220E,
1673 7
1675 12
1694 13
1704 14 L1704H
1226 7
1695 13 Q1695X,
1669 7
1671 14
1221 5 A1221V,
1668 12 M1668T,
1242 13
1676 8 M1676T, M1676I, M1676I, M1676I,
1219 7 S1219N,
1672 8 S1672Y,
1699 12
1693 14
1239 10 L1239P,
1310 13
1306 12 R1306S, R1306H,
1665 12
1305 15
1680 15 A1680T, A1680P,
1246 15
1235 10
1231 15 E1231K,
1701 10 M1701I, M1701I, M1701I,
1307 10
1228 10 Y1228H, Y1228C, Y1228F,
1678 15 N1678S,
1223 0 c.3667delG,
1697 6
1222 5 p.L1222LfsX7, L1222R,
1227 11
1674 13 F1674V,
1229 11
1215 13 I1215V,
1301 13
1696 8
1700 10
1677 12
1308 14 L1308F,
1224 4
1670 11
1240 14 E1240Q,
1225 7 E1225K, G1225K,
1238 13
1679 15
1236 14 K1236R, K1236N, K1236N,
1667 14 V1667I,
1303 11 R1303W, R1303Q,
1666 12