SCN5A Variant A582V Detail

We estimate the penetrance of LQTS for SCN5A A582V around 3% and the Brugada syndrome penetrance around 6%. SCN5A A582V was found in a total of 0 carriers in 0 papers and/or in gnomAD: 0 had Brugada syndrome, 0 had LQTS. A582V is not present in gnomAD. A582V has been functionally characterized in 0 papers. This residue is located in a Non_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 (0 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 A582V around 3% (0/10) and the Brugada syndrome penetrance around 6% (0/10).

In Silico Data

PROVEAN PolyPhen-2 BLAST-PSSM REVEL Penetrance Density BrS (%) Penetrance Density LQT3 (%)
NA NA NA 0.326 2 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: - 0 0 0 0 -
VARIANT FEATURES ALONE: - 15 15 0 0 - -
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.

A582V 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
567 15 L567Q,
568 14 R568H, R568C,
569 14 R569Q, R569W, c.1705dupC,
570 13 T570N,
571 13 S571I,
572 12 A572D, A572F, A572V, A572S,
573 11 Q573R, Q573E, Q573X,
574 11 G574E, c.1721delG,
575 10
576 9
577 8 S577N,
578 8 P578T, P578R,
579 7 G579R,
580 5
581 4 S581L,
582 0
583 4 P583L,
584 5 G584R,
585 7
586 8 p.586_587delAL, A586G, A586T,
587 8
588 9 H588R, H588N,
589 10
590 11 K590Q,
591 11
592 12 N592S, N592K,
593 13
594 13
595 14
596 14 D596G,
597 15 C597G, C597Y,