SCN5A Variant I1470F Detail

We estimate the penetrance of LQTS for SCN5A I1470F around 33% and the Brugada syndrome penetrance around 18%. SCN5A I1470F was found in a total of 0 carriers in 0 papers and/or in gnomAD: 0 had Brugada syndrome, 0 had LQTS. I1470F is not present in gnomAD. I1470F has been functionally characterized in 0 papers. This residue is located in a Mild_Hotspot region for Brugada syndrome and a Hotspot region for LQTS. In silico predictions, functional data (if available), and location in structure are equivalent to phenotyping 10 individuals for Brugada syndrome (1 diagnosed with Brugada syndrome) and 5 individuals for LQTS (1 with LQTS). These data combined with observations of carriers lead us to estimate the LQTS penetrance for SCN5A I1470F around 33% (1/10) and the Brugada syndrome penetrance around 18% (1/10).

In Silico Data

PROVEAN PolyPhen-2 BLAST-PSSM REVEL Penetrance Density BrS (%) Penetrance Density LQT3 (%)
NA NA NA 0.93 18 43
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: - 0 0 0 0 -
VARIANT FEATURES ALONE: - 15 13 1 1 - -
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.

I1470F has 74 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
414 14 M414V,
939 7 L939F,
937 13
1773 7
1765 9
943 10 S943N,
1653 14
1472 7 p.N1472del, N1472S,
1771 10 I1771T,
1777 13 V1777M, V1777L,
1764 12 c.5290delG, V1764F,
409 10 L409P, L409V,
1333 12
1656 15
417 13
934 14
1477 10 K1477N,
933 15
1471 5
935 9 L935P,
412 14 V412D,
1762 12 p.I1762del, I1762M,
1470 0
1464 10 c.4389_4396delCCTCTTTA, L1464P,
1466 6 c.4396_4397insG,
1478 13 K1478E,
1776 11
944 12
1767 12 Y1767C,
1660 14 I1660S, I1660V,
1329 13 G1329S,
1769 5
1766 9 M1766V, M1766T, M1766L,
1768 7 I1768V,
940 11 S940N,
1774 11 c.5321_5324dupACTT, N1774D,
1479 14
1473 6 F1473S, F1473C,
1334 13 I1334V,
1468 6 V1468F, V1468A,
405 15
1657 14
1462 14
1474 7
938 10
1327 13
942 11
1330 11 A1330T, A1330D, A1330P,
1772 7 L1772V,
1323 13 V1323G,
410 11 A410V,
1770 9 I1770V,
416 14 Y416C,
413 11 A413E, A413T,
1322 13 c.3963+4A>G, c.3963+2T>C,
941 13 S941F, S941N,
407 15
1337 14
1326 11 A1326S,
936 10
1763 13 V1763M, V1763L,
1465 11 p.F1465_L1480dup,
1467 5
1476 11 Q1476X, Q1476R,
1775 13 p.F1775LfsX15, F1775V,
1331 15 I1331V,
1761 13 L1761F, L1761H, c.5280delG,
1475 11 p.Q1475NfsX6, Q1475L,
1469 5 I1469V,
406 11 N406K, N406S,
1325 15 N1325S,
411 15 V411M,
932 13
1463 11 N1463Y,