Paralogue Annotation for KCNQ1 residue 198

Residue details

Gene: KCNQ1
Reference Sequences: LRG: LRG_287, Ensembl variant: ENST00000155840 / ENSP00000155840
Amino Acid Position: 198
Reference Amino Acid: I - Isoleucine
Protein Domain: Transmembrane/Linker/Pore


Paralogue Variants mapped to KCNQ1 residue 198

No paralogue variants have been mapped to residue 198 for KCNQ1.



KCNQ1GTEYVVRLWSAGCRSKYVGLWGRLRFARKP>I<SIIDLIVVVASMVVLCVG------------216
KCNQ2GVEYFVRIWAAGCCCRYRGWRGRLKFARKP>F<CVIDIMVLIASIAVLAAG------------186
KCNQ3GAEFALRIWAAGCCCRYKGWRGRLKFARKP>L<CMLDIFVLIASVPVVAVG------------216
KCNQ4GLEYIVRVWSAGCCCRYRGWQGRFRFARKP>F<CVIDFIVFVASVAVIAAG------------192
KCNQ5GLEFIIRIWSAGCCCRYRGWQGRLRFARKP>F<CVIDTIVLIASIAVVSAK------------220
KCNA1SFELVVR---------FFACPSKTDFFKNI>M<NFIDIVAIIPYFITLGTEIAEQEG------278
KCNA10TFELVLR---------FVVCPSKTDFFRNI>M<NIIDIISIIPYFATLITELVQETEP-----329
KCNA2SFEFLVR---------FFACPSKAGFFTNI>M<NIIDIVAIIPYFITLGTELAEKPE------279
KCNA3SFELLVR---------FFACPSKATFSRNI>M<NLIDIVAIIPYFITLGTELAERQ-------351
KCNA4SFEFVVR---------CFACPSQALFFKNI>M<NIIDIVSILPYFITLGTDLAQQQGG-----429
KCNA5TFELLVR---------FFACPSKAGFSRNI>M<NIIDVVAIFPYFITLGTELAEQQ---PGGG384
KCNA6TFELLVR---------FSACPSKPAFFRNI>M<NIIDLVAIFPYFITLGTELVQQQEQQPASG326
KCNA7SFELLVR---------LLVCPSKAIFFKNV>M<NLIDFVAILPYFVALGTELARQR-------265
KCNB1TMEYLLR---------FLSSPKKWKFFKGP>L<NAIDLLAILPYYVTIFLTES---N------283
KCNB2TMEYLLR---------FLSSPNKWKFFKGP>L<NVIDLLAILPYYVTIFLTES---N------287
KCNC1TFEFLMR---------VIFCPNKVEFIKNS>L<NIIDFVAILPFYLEVGLSG-----------297
KCNC2TFEFLVR---------IVFSPNKLEFIKNL>L<NIIDFVAILPFYLEVGLSG-----------334
KCNC3TFEFLMR---------ITFCPDKVEFLKSS>L<NIIDCVAILPFYLEVGLSG-----------400
KCNC4TLEFLVR---------IVCCPDTLDFVKNL>L<NIIDFVAILPFYLEVGLSG-----------333
KCND1TGEYLLR---------LFAAPSRCRFLRSV>M<SLIDVVAILPYYIGLLVP------------282
KCND2TVEYLLR---------LAAAPSRYRFVRSV>M<SIIDVVAILPYYIGLVMT------------280
KCND3TVEYLLR---------LFAAPSRYRFIRSV>M<SIIDVVAIMPYYIGLVMT------------277
KCNF1TLEYLLR---------LFSSPNKLHFALSF>M<NIVDVLAILPFYVSLTLTHL----------275
KCNG1SLEFLLR---------LIQAPSKFAFLRSP>L<TLIDLVAILPYYITLLVDGAAAGRR----K327
KCNG2SFEFLLR---------SLQAESKCAFLRAP>L<NIIDILALLPFYVSLLLGL-----A----A272
KCNG3TAECIVR---------FIVSKNKCEFVKRP>L<NIIDLLAITPYYISVLMTV-----------273
KCNG4SLEFCLR---------FVQAQDKCQFFQGP>L<NIIDILAISPYYVSLAVSEEPPEDG----E321
KCNS1SFEVSSR---------LLLAPSTRNFFCHP>L<NLIDIVSVLPFYLTLLAGVALG-D------328
KCNS2TFELVAR---------FAVAPDFLKFFKNA>L<NLIDLMSIVPFYITLVVNLV---V------281
KCNS3TGELAVR---------LAAAPCQKKFWKNP>L<NIIDFVSIIPFYATLAVDTK---E------276
KCNV1TGEFVLR---------FLCVRDRCRFLRKV>P<NIIDLLAILPFYITLLVESLSG-S------298
KCNV2TLEYLLR---------LASTPDLRRFARSA>L<NLVDLVAILPLYLQLLLECFTGEGH----Q361
cons                              > <                              

See full Alignment of Paralogues


Known Variants in KCNQ1

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.I198Vc.592A>G Inherited ArrhythmiaLQTSSIFT: deleterious
Polyphen: probably damaging
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