We estimate the penetrance of LQTS for SCN5A S401T around
38% and the Brugada syndrome penetrance around
14%. SCN5A S401T was found in a total of
0 carriers in 0 papers and/or in gnomAD:
0 had Brugada syndrome, 0 had LQTS.
S401T is not present in gnomAD.
S401T 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
S401T around 38% (1/10)
and the Brugada syndrome penetrance around 14%
In Silico Data
Penetrance Density BrS (%)
Penetrance Density LQT3 (%)
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
LITERATURE, COHORT, AND GNOMAD:
VARIANT FEATURES ALONE:
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.
S401T has 78 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.