Paralogue Annotation for KCNQ1 residue 127

Residue details

Gene: KCNQ1
Reference Sequences: LRG: LRG_287, Ensembl variant: ENST00000155840 / ENSP00000155840
Amino Acid Position: 127
Reference Amino Acid: F - Phenylalanine
Protein Domain: Transmembrane/Linker/Pore


Paralogue Variants mapped to KCNQ1 residue 127

No paralogue variants have been mapped to residue 127 for KCNQ1.



KCNQ1--------VQGRVYNFLERPT-GWKCFVYH>F<AVFLIVLVCLIFSVLSTIEQYA--------149
KCNQ2--------LQNFLYNVLERPR-G-WAFIYH>A<YVFLLVFSCLVLSVFSTIKEYE--------119
KCNQ3--------IQTLIYDALERPR-G-WALLYH>A<LVFLIVLGCLILAVLTTFKEYE--------149
KCNQ4--------LQNWVYNVLERPR-G-WAFVYH>V<FIFLLVFSCLVLSVLSTIQEHQ--------125
KCNQ5--------VQNYLYNVLERPR-G-WAFIYH>A<FVFLLVFGCLILSVFSTIPEHT--------153
KCNA1---P-EKEYQRQVWLLFEYPESSGPARVIA>I<VSVMVILISIVIFCLETLPELKDDK-DF--198
KCNA10---P-TNDIHRQFWLLFEYPESSSAARAVA>V<VSVLVVVISITIFCLETLPEFREDR-EL--247
KCNA2---P-ENEFQRQVWLLFEYPESSGPARIIA>I<VSVMVILISIVSFCLETLPIFRDEN-ED--194
KCNA3---P-RRDFQRQVWLLFEYPESSGPARGIA>I<VSVLVILISIVIFCLETLPEFRDEK-DY--265
KCNA4---P-ENEFKKQIWLLFEYPESSSPARGIA>I<VSVLVILISIVIFCLETLPEFRDDR-DL--338
KCNA5---P-RNEFQRQVWLIFEYPESSGSARAIA>I<VSVLVILISIITFCLETLPEFRDER-ELLR283
KCNA6---P-SQPFQRQVWLLFEYPESSGPARGIA>I<VSVLVILISIVIFCLETLPQFRVDG-RGGN207
KCNA7---P-RRAFARQLWLLFEFPESSQAARVLA>V<VSVLVILVSIVVFCLETLPDFRDDR-DGTG176
KCNB1NTC--CAEKRKKLWDLLEKPNSSVAAKILA>I<ISIMFIVLSTIALSLNTLPELQSLD-EF--220
KCNB2NTC--CPDKRKKLWDLLEKPNSSVAAKILA>I<VSILFIVLSTIALSLNTLPELQETD-EF--224
KCNC1PGGF-WRRWQPRIWALFEDPYSSRYARYVA>F<ASLFFILVSITTFCLETHERFNPIV-NK--221
KCNC2SGR--WRRLQPRMWALFEDPYSSRAARFIA>F<ASLFFILVSITTFCLETHEAFNI---VK--258
KCNC3GGTW-WRRWQPRVWALFEDPYSSRAARYVA>F<ASLFFILISITTFCLETHEGFIHIS-NK--321
KCNC4SGG--CRGWQPRMWALFEDPYSSRAARVVA>F<ASLFFILVSITTFCLETHEAFNI---DR-N256
KCND1---PAGSSLRQRLWRAFENPHTSTAALVFY>Y<VTGFFIAVSVIANVVETIPCRGSAR-RS--217
KCND2---PTMT-ARQRVWRAFENPHTSTMALVFY>Y<VTGFFIAVSVIANVVETVPCGS-SP-GH--215
KCND3---PSLS-FRQTMWRAFENPHTSTLALVFY>Y<VTGFFIAVSVITNVVETVPCGT-VP-G---212
KCNF1EGR--WRRCQKCVWKFLEKPESSCPARVVA>V<LSFLLILVSSVVMCMGTIPELQVLD-AE--213
KCNG1EGRL-GR-CMRRLRDMVERPHSGLPGKVFA>C<LSVLFVTVTAVNLSVSTLPSLREEEE-Q--258
KCNG2RGRL-QR-GRRRLRDVVDNPHSGLAGKLFA>C<VSVSFVAVTAVGLCLSTMPDIRAEEE-R--208
KCNG3EAAP-SRRWLERMRRTFEEPTSSLAAQILA>S<VSVVFVIVSMVVLCASTLPDWRN-AAAD--202
KCNG4SSRW-GL-CMNRLREMVENPQSGLPGKVFA>C<LSILFVATTAVSLCVSTMPDLRAEED-Q--252
KCNS1AAR--CGRLRRRLWLTMENPGYSLPSKLFS>C<VSISVVLASIAAMCIHSLPEYQARE-AA--251
KCNS2GQP--LGNFRRQLWLALDNPGYSVLSRVFS>I<LSILVVMGSIITMCLNSLPDFQIPD-SQ--218
KCNS3TLR--FGQLRKKIWIRMENPAYCLSAKLIA>I<SSLSVVLASIVAMCVHSMSEFQNED-GE--216
KCNV1QGP--CPTVRQKLWNILEKPGSSTAARIFG>V<ISIIFVVVSIINMALMSAEL----------234
KCNV2DMRF-YGPQRRRLWNLMEKPFSSVAAKAIG>V<ASSTFVLVSVVALALNTVEEMQQHS-GQ--291
cons                              > <                              

See full Alignment of Paralogues


Known Variants in KCNQ1

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.F127Lc.381C>A Inherited ArrhythmiaLQTSSIFT: tolerated
Polyphen: possibly 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