K591T Summary

SCN5A K591T was found in 0 papers (see below) with a total of 0 carriers: 0 had BrS1, 0 had LQT3, and 0 had other disease. K591T is not present in gnomAD. K591T has been functionally characterized in 0 papers. Other variants at the same resdue are K591E .K591M .K591N .K591N .K591Q .K591R .K591T . This residue is located in a Non_Hotspot region for BrS1 and in a Non_Hotspot region for Long QT syndrome.

K591T 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 0.479

K591T 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
576 14.7
577 14.2
578 13.7
579 13.2 G579R G579R
580 12.6
581 12 S581L
582 11.4
583 10.7
584 10.1 G584R
585 9.3
586 8.5 A586T
587 7.6
588 6.6
589 5.4
590 3.8
592 3.8 N592K N592K N592S
593 5.4
594 6.6
595 7.6
596 8.5
597 9.3
598 10.1
599 10.7 G599R G599R
600 11.4
601 12
602 12.6
603 13.2
604 13.7 L604V
605 14.2
606 14.7