SCN5A Variant G1481V
Summary of observed carriers, functional annotations, and structural context for SCN5A G1481V. Data combine curated literature, international cohorts, and gnomAD observations.
Estimated LQT3 penetrance
64%
3/11 effective observations
Estimated BrS1 penetrance
13%
1/11 effective observations
Total carriers
1
0 BrS1 · 1 LQT3 · 0 unaffected
Variant features alone are equivalent to phenotyping 1 individuals for Brugada syndrome and 2 individuals for LQT3.
In silico predictors
| PROVEAN | PolyPhen-2 | BLAST-PSSM | REVEL | Penetrance Density BrS (%) | Penetrance Density LQT3 (%) |
|---|---|---|---|---|---|
| -6.58 | 0.726 | -2.69 | 0.893 | 7 | 75 |
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 |
|---|---|---|---|---|---|---|---|
| 30059973 | 2018 | 1 | 1 | 0 | 0 | ||
| Literature, cohort, and gnomAD | – | 1 | 0 | 1 | 0 | – | |
| Variant features alone | – | 15 | 12 | 2 | 1 | – | – |
Totals may differ from individual publications due to duplicate patients removed during curation.
Functional data
Peak and late/persistent current values are relative to wild-type (100% indicates no change). V1/2 activation and inactivation denote the membrane potentials (mV) at which half-maximal current is achieved.
| PubMed ID | Year | Cell Type | Peak Current (% WT) | V1/2 Activation (mV) | V1/2 Inactivation (mV) | Late/Persistent Current (% WT) |
|---|---|---|---|---|---|---|
| 30059973 | 2018 |
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 |
|---|---|---|
| 1480 | 4 | c.4437+5G>A, c.4438-1C>T, |
| 1773 | 13 | |
| 1486 | 12 | F1486L, p.F1486del, F1486L, F1486L, |
| 1652 | 14 | M1652T, M1652R, |
| 1777 | 12 | V1777M, V1777L, V1777L, |
| 1485 | 12 | |
| 1487 | 13 | M1487L, M1487L, M1487K, |
| 1492 | 8 | |
| 1477 | 7 | K1477N, K1477N, |
| 1491 | 13 | Q1491H, Q1491H, |
| 1493 | 13 | p.K1493del, K1493X, K1493R, |
| 1478 | 7 | K1478E, |
| 1319 | 14 | G1319V, |
| 1495 | 8 | Y1495S, |
| 1774 | 13 | N1774D, c.5321_5324dupACTT, |
| 1479 | 8 | |
| 1473 | 13 | F1473S, F1473C, |
| 1496 | 9 | |
| 1474 | 11 | |
| 1481 | 0 | G1481R, G1481R, G1481E, G1481V, |
| 1781 | 14 | E1781G, E1781D, E1781D |
| 1318 | 14 | |
| 1499 | 10 | |
| 1488 | 14 | T1488R, |
| 1321 | 13 | R1321K, |
| 1498 | 14 | M1498V, M1498T, M1498R, |
| 1500 | 13 | p.K1500del, |
| 1482 | 3 | |
| 1322 | 11 | c.3963+2T>C, c.3963+4A>G, |
| 1476 | 9 | Q1476X, Q1476R, |
| 1484 | 10 | |
| 1497 | 13 | |
| 1475 | 10 | p.Q1475NfsX6, Q1475L, |
| 1483 | 7 | Q1483H, Q1483H, |
| 1494 | 14 | |
| 1325 | 14 | N1325S, |
| 1503 | 15 | S1503Y, |
| 1489 | 12 | E1489D, E1489D, |