SCN5A Variant M520V Detail

We estimate the penetrance of LQTS for SCN5A M520V around 0% and the Brugada syndrome penetrance around 9%. SCN5A M520V was found in a total of 9 carriers in 0 papers and/or in gnomAD: 0 had Brugada syndrome, 0 had LQTS. M520V is present in 9 alleles in gnomAD. M520V has been functionally characterized in 0 papers. This residue is located in a Mild_Hotspot region for Brugada syndrome and a Non_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 (0 with LQTS). These data combined with observations of carriers lead us to estimate the LQTS penetrance for SCN5A M520V around 0% (0/19) and the Brugada syndrome penetrance around 9% (1/19).

In Silico Data

PROVEAN PolyPhen-2 BLAST-PSSM REVEL Penetrance Density BrS (%) Penetrance Density LQT3 (%)
-0.63 0 -0.15 0.48 17 1
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: - 9 9 0 0 -
VARIANT FEATURES ALONE: - 15 14 0 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.

M520V has 31 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
505 15 A505E,
506 14 M506K,
507 14 p.N507_L515dup,
508 13
509 13
510 12
511 11
512 11 T512I,
513 10 R513C, R513P, R513H, c.1537delC,
514 9 G514C,
515 8
516 8
517 7 R517S,
518 5
519 4 S519F,
520 0 M520V, M520R,
521 4 K521E, c.1562delA,
522 5 P522S,
523 7 R523H, R523S, R523C,
524 8 c.1570_1571insG, S524Y,
525 8 S525G,
526 9 R526C, R526H,
527 10 G527R,
528 11 S528R,
529 11
530 12 F530S, F530V,
531 13 T531A, T531I,
532 13 F532L, F532C,
533 14 R533C, R533S, R533H,
534 14
535 15 R535X, R535G, R535Q,