Paralogue Annotation for KCNQ1 residue 398

Residue details

Gene: KCNQ1
Reference Sequences: LRG: LRG_287, Ensembl variant: ENST00000155840 / ENSP00000155840
Amino Acid Position: 398
Reference Amino Acid: K - Lysine
Protein Domain: C-terminus


Paralogue Variants mapped to KCNQ1 residue 398

No paralogue variants have been mapped to residue 398 for KCNQ1.



KCNQ1---------------------STWKI-YIR>K<-A--PRSH----------------------403
KCNQ2---------------------STWQY-YER>T<-VTVPMYSS--QT-QTY------------G380
KCNQ3---------------------ATWRF-YES>V<-VSFPFFR----------------------412
KCNQ4---------------------ATWYY-YDS>I<-L--PSFRELALL-FEH------------V386
KCNQ5---------------------ATWK----->-<----PHLK----------------------398
KCNA1--------------------------DL-S>R<--RS-----SS-T-MS-------------K451
KCNA10---------------------------L-->N<--SV-----GS-R-MG-------------S493
KCNA2-------------------------DLK-K>S<--RS-----AS-T-IS-------------K455
KCNA3-------------------------ELR-K>A<--RS-----NS-T-LS-------------K526
KCNA4-------------------------KFR-S>S<--TS-----SS-L-GD-------------K608
KCNA5-KVSG-SRGSFCKAGG------T--LEN-->A<--DS----ARR-G-SC--------------581
KCNA6--------------QP------A--PDL-->R<--AT-----DN-G-LG--------------497
KCNA7----------------------G--PLE-->G<--KA-----NG-G-LV--------------433
KCNB1---------------------------M-K>-<-DAF-----AR-S-IE-----MMD---IVV465
KCNB2---------------------------L-K>-<-DAF-----AR-S-ME-----LID---VAV469
KCNC1---------------------VNSPHHS-T>Q<--SD-----TC-P-LA-------------Q492
KCNC2---------------------LNMACNS-T>Q<--SD-----TC-L-GK-------------D529
KCNC3YPAGPHTHPGLLRGGAGGLGIMGLPPLP-A>P<--GE-----PC-P-LA-------------Q650
KCNC4---------------------ETSPRDS-T>C<--SD-----TS-PPAR-------------E529
KCND1---------------------------F-L>Q<YKQN-----GG-L-ED-----SG--S-GEE463
KCND2---------------------------Y-M>Q<SKRN-----GL-L-SN-----QLQ-SSEDE463
KCND3---------------------------Y-L>H<SKRN-----GL-L-NE-----ALELTGTPE461
KCNF1---------------------------G-K>T<-GGS-----RS-D-LD-----NLP---PEP456
KCNG1---------------------------S-Q>-<---D-----SD-I-LFGSAS--SD---TRD511
KCNG2---------------------------T-E>-<---D-----SS-Q-GPDSAGLADD---SAD458
KCNG3---------------------------F-L>-<------------------------------435
KCNG4---------------------------H-V>-<---A-----SE-H-EL-----MND---VND506
KCNS1--------------------------GV-S>-<-EAS-----LE-T-SR-----ETS---QEG507
KCNS2---------------------------L-R>-<-DYY-----AH-K-VK-----SLM---ASL459
KCNS3---------------------------I-R>-<-DIY-----AQ-R-MH-----TFI---TSL455
KCNV1---------------------------L-R>-<-DVY-----AR-S-IM-----EML-----R481
KCNV2--------------------------KI-A>-<-ECL-----LG-S-NP-----QLT---PRQ543
cons                              > <                              

See full Alignment of Paralogues


Known Variants in KCNQ1

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.K398Rc.1193A>G Inherited ArrhythmiaLQTSSIFT: tolerated
Polyphen: benign
ReportsInherited ArrhythmiaLQTS Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test. Heart Rhythm. 2009 6(9):1297-303. 19716085