Paralogue Annotation for KCNQ1 residue 308

Residue details

Gene: KCNQ1
Reference Sequences: LRG: LRG_287, Ensembl variant: ENST00000155840 / ENSP00000155840
Amino Acid Position: 308
Reference Amino Acid: V - Valine
Protein Domain: Transmembrane/Linker/Pore


Paralogue Variants mapped to KCNQ1 residue 308

No paralogue variants have been mapped to residue 308 for KCNQ1.



KCNQ1AEKDAVN-----ESGRVEFGSYADALWWGV>V<TVTTIGYGDKVPQTWVGKTIASCFSVFAIS338
KCNQ2AEKGE----------NDHFDTYADALWWGL>I<TLTTIGYGDKYPQTWNGRLLAATFTLIGVS303
KCNQ3VEKDVPEVDAQGEEMKEEFETYADALWWGL>I<TLATIGYGDKTPKTWEGRLIAATFSLIGVS342
KCNQ4AEKDA----------NSDFSSYADSLWWGT>I<TLTTIGYGDKTPHTWLGRVLAAGFALLGIS309
KCNQ5VEKDA----------NKEFSTYADALWWGT>I<TLTTIGYGDKTPLTWLGRLLSAGFALLGIS337
KCNA1AEAEE---------AESHFSSIPDAFWWAV>V<SMTTVGYGDMYPVTIGGKIVGSLCAIAGVL398
KCNA10AEVDE---------PESHFSSIPDGFWWAV>V<TMTTVGYGDMCPTTPGGKIVGTLCAIAGVL447
KCNA2AEADE---------RESQFPSIPDAFWWAV>V<SMTTVGYGDMVPTTIGGKIVGSLCAIAGVL400
KCNA3AEADD---------PTSGFSSIPDAFWWAV>V<TMTTVGYGDMHPVTIGGKIVGSLCAIAGVL470
KCNA4AEADE---------PTTHFQSIPDAFWWAV>V<TMTTVGYGDMKPITVGGKIVGSLCAIAGVL550
KCNA5AEADN---------QGTHFSSIPDAFWWAV>V<TMTTVGYGDMRPITVGGKIVGSLCAIAGVL506
KCNA6AEADD---------DDSLFPSIPDAFWWAV>V<TMTTVGYGDMYPMTVGGKIVGSLCAIAGVL448
KCNA7AEVDR---------VDSHFTSIPESFWWAV>V<TMTTVGYGDMAPVTVGGKIVGSLCAIAGVL384
KCNB1AEKDE---------DDTKFKSIPASFWWAT>I<TMTTVGYGDIYPKTLLGKIVGGLCCIAGVL403
KCNB2AEKDE---------DATKFTSIPASFWWAT>I<TMTTVGYGDIYPKTLLGKIVGGLCCIAGVL407
KCNC1AERIGAQPNDPSASEHTHFKNIPIGFWWAV>V<TMTTLGYGDMYPQTWSGMLVGALCALAGVL426
KCNC2AERVGAQPNDPSASEHTQFKNIPIGFWWAV>V<TMTTLGYGDMYPQTWSGMLVGALCALAGVL463
KCNC3AERIGADPDDILGSNHTYFKNIPIGFWWAV>V<TMTTLGYGDMYPKTWSGMLVGALCALAGVL529
KCNC4AERIGARPSDPRGNDHTDFKNIPIGFWWAV>V<TMTTLGYGDMYPKTWSGMLVGALCALAGVL462
KCND1AEKGT---------NKTNFTSIPAAFWYTI>V<TMTTLGYGDMVPSTIAGKIFGSICSLSGVL398
KCND2AEKGS---------SASKFTSIPAAFWYTI>V<TMTTLGYGDMVPKTIAGKIFGSICSLSGVL396
KCND3AEKGS---------SASKFTSIPASFWYTI>V<TMTTLGYGDMVPKTIAGKIFGSICSLSGVL393
KCNF1MEQSH---------PETLFKSIPQSFWWAI>I<TMTTVGYGDIYPKTTLGKLNAAISFLCGVI396
KCNG1IENEM-----A---DSPEFTSIPACYWWAV>I<TMTTVGYGDMVPRSTPGQVVALSSILSGIL450
KCNG2AEREL-----G---ARRDFSSVPASYWWAV>I<SMTTVGYGDMVPRSLPGQVVALSSILSGIL395
KCNG3LEHGL-----DLETSNKDFTSIPAACWWVI>I<SMTTVGYGDMYPITVPGRILGGVCVVSGIV399
KCNG4AEKES-----G---RVLEFTSIPASYWWAI>I<SMTTVGYGDMVPRSVPGQMVALSSILSGIL444
KCNS1AEKEE----------DVGFNTIPACWWWGT>V<SMTTVGYGDVVPVTVAGKLAASGCILGGIL447
KCNS2IEKEE----------NEGLATIPACWWWAT>V<SMTTVGYGDVVPGTTAGKLTASACILAGIL400
KCNS3VEKDD---------HTSSLTSIPICWWWAT>I<SMTTVGYGDTHPVTLAGKLIASTCIICGIL396
KCNV1AEQSI---------PDTTFTSVPCAWWWAT>T<SMTTVGYGDIRPDTTTGKIVAFMCILSGIL418
KCNV2VEHDV---------PSTNFTTIPHSWWWAA>V<SISTVGYGDMYPETHLGRFFAFLCIAFGII483
cons                              > <                              

See full Alignment of Paralogues


Known Variants in KCNQ1

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.V308Dc.923T>A Inherited ArrhythmiaLQTSSIFT: deleterious
Polyphen: probably damaging
ReportsInherited ArrhythmiaLQTS Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice. JAMA. 2005 294(23):2975-80. 16414944