Paralogue Annotation for KCNQ1 residue 203

Residue details

Gene: KCNQ1
Reference Sequences: LRG: LRG_287, Ensembl variant: ENST00000155840 / ENSP00000155840
Amino Acid Position: 203
Reference Amino Acid: L - Leucine
Protein Domain: Transmembrane/Linker/Pore


Paralogue Variants mapped to KCNQ1 residue 203

No paralogue variants have been mapped to residue 203 for KCNQ1.



KCNQ1VRLWSAGCRSKYVGLWGRLRFARKPISIID>L<IVVVASMVVLCVG----------------S217
KCNQ2VRIWAAGCCCRYRGWRGRLKFARKPFCVID>I<MVLIASIAVLAAG----------------S187
KCNQ3LRIWAAGCCCRYKGWRGRLKFARKPLCMLD>I<FVLIASVPVVAVG----------------N217
KCNQ4VRVWSAGCCCRYRGWQGRFRFARKPFCVID>F<IVFVASVAVIAAG----------------T193
KCNQ5IRIWSAGCCCRYRGWQGRLRFARKPFCVID>T<IVLIASIAVVSAK----------------T221
KCNA1VR---------FFACPSKTDFFKNIMNFID>I<VAIIPYFITLGTEIAEQEG-------N-QK281
KCNA10LR---------FVVCPSKTDFFRNIMNIID>I<ISIIPYFATLITELVQETEP---------S330
KCNA2VR---------FFACPSKAGFFTNIMNIID>I<VAIIPYFITLGTELAEKPE-------DAQQ283
KCNA3VR---------FFACPSKATFSRNIMNLID>I<VAIIPYFITLGTELAERQ----------GN353
KCNA4VR---------CFACPSQALFFKNIMNIID>I<VSILPYFITLGTDLAQQQGG------GNGQ433
KCNA5VR---------FFACPSKAGFSRNIMNIID>V<VAIFPYFITLGTELAEQQ---PGGGGGGQN389
KCNA6VR---------FSACPSKPAFFRNIMNIID>L<VAIFPYFITLGTELVQQQEQQPASGGGGQN331
KCNA7VR---------LLVCPSKAIFFKNVMNLID>F<VAILPYFVALGTELARQR----------GV267
KCNB1LR---------FLSSPKKWKFFKGPLNAID>L<LAILPYYVTIFLTES---N--------KSV286
KCNB2LR---------FLSSPNKWKFFKGPLNVID>L<LAILPYYVTIFLTES---N--------KSV290
KCNC1MR---------VIFCPNKVEFIKNSLNIID>F<VAILPFYLEVGLSG-------------LSS300
KCNC2VR---------IVFSPNKLEFIKNLLNIID>F<VAILPFYLEVGLSG-------------LSS337
KCNC3MR---------ITFCPDKVEFLKSSLNIID>C<VAILPFYLEVGLSG-------------LSS403
KCNC4VR---------IVCCPDTLDFVKNLLNIID>F<VAILPFYLEVGLSG-------------LSS336
KCND1LR---------LFAAPSRCRFLRSVMSLID>V<VAILPYYIGLLVP-----------------282
KCND2LR---------LAAAPSRYRFVRSVMSIID>V<VAILPYYIGLVMT-----------------280
KCND3LR---------LFAAPSRYRFIRSVMSIID>V<VAIMPYYIGLVMT-----------------277
KCNF1LR---------LFSSPNKLHFALSFMNIVD>V<LAILPFYVSLTLTHL-----------GARM279
KCNG1LR---------LIQAPSKFAFLRSPLTLID>L<VAILPYYITLLVDGAAAGRR----KPGAGN332
KCNG2LR---------SLQAESKCAFLRAPLNIID>I<LALLPFYVSLLLGL-----A----AGPGGT277
KCNG3VR---------FIVSKNKCEFVKRPLNIID>L<LAITPYYISVLMTV-----------FTGEN278
KCNG4LR---------FVQAQDKCQFFQGPLNIID>I<LAISPYYVSLAVSEEPPEDG----ERPSGS326
KCNS1SR---------LLLAPSTRNFFCHPLNLID>I<VSVLPFYLTLLAGVALG-D--------QGG331
KCNS2AR---------FAVAPDFLKFFKNALNLID>L<MSIVPFYITLVVNLV---V--------EST284
KCNS3VR---------LAAAPCQKKFWKNPLNIID>F<VSIIPFYATLAVDTK---E--------EES279
KCNV1LR---------FLCVRDRCRFLRKVPNIID>L<LAILPFYITLLVESLSG-S--------QTT301
KCNV2LR---------LASTPDLRRFARSALNLVD>L<VAILPLYLQLLLECFTGEGH----QRGQTV366
cons                              > <                              

See full Alignment of Paralogues


Known Variants in KCNQ1

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.L203Pc.608T>C Inherited ArrhythmiaLQTSSIFT: deleterious
Polyphen: probably damaging
ReportsInherited ArrhythmiaLQTS A novel KCNQ1 variant (L203P) associated with torsades de pointes-related syncope in a Steinert syndrome patient. Can J Cardiol. 2011 27(2):263.e5-12. 21459285