R53L Summary

SCN5A R53L was found in 0 papers (see below) with a total of 0 carriers: 0 had BrS1, 0 had LQT3, and 0 had other disease. R53L is not present in gnomAD. R53L has been functionally characterized in 0 papers. Other variants at the same resdue are R53G .R53L .R53P .R53Q .R53W . This residue is located in a Non_Hotspot region for BrS1 and in a Mild_Hotspot region for Long QT syndrome.

R53L Predictions

PROVEAN scores less than -2 are considered deleterious. REVEL scores higher than 0.5 or 0.75 is 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. PAM scores reflect the chemistry difference between WT and variant amino acid (more negative being greater difference between the two). BLAST-PSSM reflects the evolutionary conservation of residue substitutions, more negative numbers indicate fewer observations of the specific substitution than is expected.

SIFT Sift Score PROVEAN Score Polyphen2 Polyphen2 Score eaRate blastPssm pamScore REVEL
NA NA NA NA NA NA NA NA 0.407

R53L has 30 neighbors within 15 ångströms that have been found in individuals.

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.

ResidueNumber Distance(Å) Variants
38 14.7
39 14.2
40 13.7
41 13.2
42 12.6
43 12 R43Q
44 11.4
45 10.7
46 10.1
47 9.3
48 8.5 E48K
49 7.6
50 6.6
51 5.4 A51V
52 3.8 P52S
54 3.8
55 5.4
56 6.6
57 7.6
58 8.5
59 9.3
60 10.1 A60P
61 10.7
62 11.4
63 12 K63N K63N
64 12.6
65 13.2
66 13.7
67 14.2
68 14.7