K63Q Summary

SCN5A K63Q was found in 0 papers (see below) with a total of 0 carriers: 0 had BrS1, 0 had LQT3, and 0 had other disease. K63Q is not present in gnomAD. K63Q has been functionally characterized in 0 papers. Other variants at the same resdue are K63E .K63M .K63N .K63N .K63Q .K63R .K63T . This residue is located in a Non_Hotspot region for BrS1 and in a Non_Hotspot region for Long QT syndrome.

K63Q 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 0.31

K63Q 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
48 14.7 E48K
49 14.2
50 13.7
51 13.2 A51V
52 12.6 P52S
53 12 R53Q
54 11.4
55 10.7
56 10.1
57 9.3
58 8.5
59 7.6
60 6.6 A60P
61 5.4
62 3.8
64 3.8
65 5.4
66 6.6
67 7.6
68 8.5
69 9.3 G69D
70 10.1 N70K N70K N70S
71 10.7
72 11.4
73 12
74 12.6 E74D E74D
75 13.2
76 13.7
77 14.2
78 14.7