SCN5A Variant S1282A Detail

We estimate the penetrance of LQTS for SCN5A S1282A around 11% and the Brugada syndrome penetrance around 18%. SCN5A S1282A was found in a total of 1 carriers in 0 papers and/or in gnomAD: 0 had Brugada syndrome, 0 had LQTS. S1282A is present in 1 alleles in gnomAD. S1282A has been functionally characterized in 0 papers. This residue is located in a Mild_Hotspot region for Brugada syndrome and a Mild_Hotspot region for LQTS. In silico predictions, functional data (if available), and location in structure are equivalent to phenotyping 10 individuals for Brugada syndrome (2 diagnosed with Brugada syndrome) and 5 individuals for LQTS (0 with LQTS). These data combined with observations of carriers lead us to estimate the LQTS penetrance for SCN5A S1282A around 11% (0/11) and the Brugada syndrome penetrance around 18% (2/11).

In Silico Data

PROVEAN PolyPhen-2 BLAST-PSSM REVEL Penetrance Density BrS (%) Penetrance Density LQT3 (%)
-2.62 0.499 2.14 0.841 28 15
PROVEAN scores less than -2 are considered deleterious. REVEL scores higher than 0.5 or 0.75 are considered likely pathogenic (higher sensitivity with the former cutoff, higher specificity with the latter cutoff). A PolyPhen-2 score of 0.85 or greater is considered likely pathogenic. BLAST-PSSM reflects the evolutionary conservation of residue substitutions, more negative numbers indicate fewer observations of the specific substitution than is expected. Penetrance Density is our previously published method to calculate the average BrS/LQTS probability density in a shell of residues surrounding a residue of interest (Kroncke et al. 2019).

Reported Carrier Data

PubMed ID Year Carriers Unaffected LQT3 BrS1 Other Other Disease
LITERATURE, COHORT, AND GNOMAD: - 1 1 0 0 -
VARIANT FEATURES ALONE: - 15 13 0 2 - -
Summary totals might not agree with the literature table because of duplicate patients, which were excluded from the total counts. We do not distinguish here between multiple missense codons. Missense variants are combined across degenerate codon substitutions since codon-level data were not consistently available for curation.

S1282A has 53 previously observed neighbors within 15 angstroms

A residue within a folded protein on average has nearest neighbors that fall roughly into two shells: a "nearest" neighbor around 5-6 angstroms and a second shell around 11 angstroms. All variants shown in the rightmost column have been observed in at least one individual in the literature or gnomAD.

Neighbor Distance (Angstroms) Variants Observed in Individuals
1245 11 M1245I,
1218 13 S1218I, S1218T,
1281 4 c.3840+1G>A, V1281F,
1304 11 T1304M,
1243 7 D1243N,
1274 12
1285 5
1258 15
1299 11 c.3894delC,
1252 13
1283 4 L1283M,
1241 14
1309 12 R1309H, R1309C,
1288 10 A1288G,
1242 11
1219 15 S1219N,
1251 9 V1251M,
1279 5 V1279I,
1239 14 L1239P,
1306 7 R1306S, R1306H,
1244 10 K1244E,
1286 7
1305 9
1273 14 W1273C, c.3816delG,
1282 0 S1282A,
1246 9
1302 8 p.L1302Vfs18,
1247 5 T1247I,
1307 13
1289 11
1275 11 D1275N,
1255 14 L1255M,
1222 14 p.L1222LfsX7, L1222R,
1300 14
1254 11
1215 14 I1215V,
1301 11
1214 15 M1214T,
1253 12 E1253G,
1284 6
1291 15
1280 6
1308 13 L1308F,
1250 7
1240 12 E1240Q,
1248 9
1287 9
1276 10
1290 14
1278 6 I1278N,
1249 10 V1249D,
1277 9
1303 8 R1303Q, R1303W,