I76M Summary

SCN5A I76M was found in 0 papers (see below) with a total of 0 carriers: 0 had BrS1, 0 had LQT3, and 0 had other disease. I76M is not present in gnomAD. I76M has been functionally characterized in 0 papers. Other variants at the same resdue are I76F .I76L .I76M .I76N .I76S .I76T .I76V . This residue is located in a Non_Hotspot region for BrS1 and in a Non_Hotspot region for Long QT syndrome.

I76M 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 0.579

I76M 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
61 14.7
62 14.2
63 13.7 K63N K63N
64 13.2
65 12.6
66 12
67 11.4
68 10.7
69 10.1 G69D
70 9.3 N70K N70K N70S
71 8.5
72 7.6
73 6.6
74 5.4 E74D E74D
75 3.8
77 3.8
78 5.4
79 6.6 P79A
80 7.6
81 8.5
82 9.3 D82E D82E
83 10.1
84 10.7 D84G D84N
85 11.4
86 12 F86L F86L F86L
87 12.6
88 13.2 S88G
89 13.7
90 14.2
91 14.7