SCN5A Variant W1271C

Summary of observed carriers, functional annotations, and structural context for SCN5A W1271C. Data combine curated literature, international cohorts, and gnomAD observations.

Estimated LQT3 penetrance

15%

0/11 effective observations

Estimated BrS1 penetrance

50%

5/11 effective observations

Total carriers

1

1 BrS1 · 0 LQT3 · 0 unaffected

W1271C has not been reported in gnomAD. This residue resides in a Mild_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 0 individuals for LQT3.

In silico predictors

Variant-level computational predictors.
PROVEAN PolyPhen-2 BLAST-PSSM REVEL Penetrance Density BrS (%) Penetrance Density LQT3 (%)
-12.66 1 -6.29 0.941 61 12

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
20129283 2010 1 0 1 0
Literature, cohort, and gnomAD 1 0 0 1
Variant features alone 15 11 0 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)
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 W1271C.
Neighbour residue Distance (Å) Observed variants
1267 13
1328 10 V1328M,
1271 0 W1271C, W1271C,
1315 8
1274 6
1314 11 c.3940_3941delCT,
1320 13 M1320I, M1320I, M1320I,
1666 14
1272 6
1270 5 A1270S,
1309 9 R1309H, R1309C,
1265 13
1313 9
1279 15 V1279I,
1329 14 G1329S,
1310 10
1316 10 R1316L, R1316Q,
1306 15 R1306S, R1306H,
1305 13
1273 9 c.3816delG, W1273C, W1273C,
1663 14
1324 10
1317 14 F1317C,
1327 12
1257 13
1268 11 T1268N, T1268S, T1268S,
1307 12
1275 8 D1275N,
1321 12 R1321K,
1323 14 V1323G,
1254 14
1215 13 I1215V,
1212 13 p.I1212del,
1253 14 E1253G,
1211 14
1312 5
1326 14 A1326S
1311 7 L1311P,
1308 9 L1308F,
1250 15
1670 14
1331 14 I1331V,
1269 6 N1269S,
1325 11 N1325S,
1276 12
1278 12 I1278N,
1266 10
1261 12
1208 14 E1208K, E1208X,
1277 11