SCN5A Variant D1062H
Summary of observed carriers, functional annotations, and structural context for SCN5A D1062H. Data combine curated literature, international cohorts, and gnomAD observations.
Estimated LQT3 penetrance
3%
0/11 effective observations
Estimated BrS1 penetrance
9%
1/11 effective observations
Total carriers
1
0 BrS1 · 0 LQT3 · 1 unaffected
Variant features alone are equivalent to phenotyping 1 individuals for Brugada syndrome and 0 individuals for LQT3.
In silico predictors
PROVEAN | PolyPhen-2 | BLAST-PSSM | REVEL | Penetrance Density BrS (%) | Penetrance Density LQT3 (%) |
---|---|---|---|---|---|
-2.44 | 0.484 | -0.61 | 0.547 | 3 | 1 |
PROVEAN scores below -2 suggest deleterious impact. REVEL scores above 0.5–0.75 are often interpreted as likely pathogenic. PolyPhen-2 scores above 0.85 are typically pathogenic. Penetrance density summarises neighbouring residue risk (Kroncke et al. 2019).
Reported carrier data
Source | Year | Carriers | Unaffected | LQT3 | BrS1 | Other | Other Disease |
---|---|---|---|---|---|---|---|
Literature, cohort, and gnomAD | – | 1 | 1 | 0 | 0 | – | |
Variant features alone | – | 15 | 14 | 0 | 1 | – | – |
Totals may differ from individual publications due to duplicate patients removed during curation.
Nearby variants
Neighbouring residues within 15 Ångström provide structural context. Variants listed in the right-most column have been observed clinically or in gnomAD.
Neighbour residue | Distance (Å) | Observed variants |
---|---|---|
1047 | 15 | c.3140_3141dupTG, |
1048 | 14 | p.P1048SfsX96, c.3142_3143insTG, P1048S, |
1049 | 14 | |
1050 | 13 | p.A1050CfsX9, A1050T, p.A1050DfsX9, |
1051 | 13 | V1051A, |
1052 | 12 | A1052D, p.A1052CfsX7 |
1053 | 11 | E1053K, |
1054 | 11 | |
1055 | 10 | D1055G, |
1056 | 9 | T1056A, |
1057 | 8 | |
1058 | 8 | c.3171_3172delTGinsA, |
1059 | 7 | Q1059X, |
1060 | 5 | |
1061 | 4 | E1061D, E1061D, |
1062 | 0 | D1062H, |
1063 | 4 | E1063G, |
1064 | 5 | p.E1064del, |
1065 | 7 | |
1066 | 8 | S1066G, |
1067 | 8 | L1067R, |
1068 | 9 | G1068A, G1068D, |
1069 | 10 | T1069M, |
1070 | 11 | |
1071 | 11 | E1071K, p.E1071GfsX76, |
1072 | 12 | p.E1072del, |
1073 | 13 | |
1074 | 13 | S1074R, S1074R, S1074R, S1074G, |
1075 | 14 | |
1076 | 14 | |
1077 | 15 | c.3228+2delT, |