SCN5A Variant I790M Detail

We estimate the penetrance of LQTS for SCN5A I790M around 4% and the Brugada syndrome penetrance around 10%. SCN5A I790M was found in a total of 0 carriers in 0 papers and/or in gnomAD: 0 had Brugada syndrome, 0 had LQTS. I790M is not present in gnomAD. I790M 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 I790M around 4% (0/10) and the Brugada syndrome penetrance around 10% (0/10).

In Silico Data

PROVEAN PolyPhen-2 BLAST-PSSM REVEL Penetrance Density BrS (%) Penetrance Density LQT3 (%)
NA NA NA 0.569 6 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.

I790M has 40 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
758 13 G758E,
811 13 c.2435_2436+3delTGGTAinsCGCCT, R811H, R811G,
773 15 P773S,
760 12 p.F760SfsX5,
780 14
776 13 p.Y776del,
765 12
759 15 p.I759FfsX6, I759V, c.2274delG,
792 6
764 10 M764K, M764R,
777 12 F777L,
791 5 L791F,
806 14 V806M,
797 12 G797V,
788 7 I788V,
798 13
782 13 N782T,
793 6 L793F,
762 13
810 10
767 15
814 11 R814Q,
807 10
813 11 c.2437-5C>A, c.2436+12G>A,
757 11
768 13
786 6
817 15 K817E,
761 10
809 14
790 0
784 11 F784L,
763 15 E763D, E763K,
796 11
785 10 D785N,
783 10 I783T,
789 5 V789I, V789A,
795 10
787 5
794 6