No paralogue variants have been mapped to residue 1119 for KCNH2.
KCNH2 | L-----PVSPLP-TLTLDSLSQVSQFMACE>E<LPPGAPELPQ-------------------- | 1129 |
KCNH1 | H-----ELKEDIKALNAKMTNIEKQLSEIL>R<ILTSRRS----------------------- | 963 |
KCNH3 | STSGLLQPLCVDTGASSYCLQPPAGSVLSG>T<WPHPRPGPPPL--MAPWPWG-------PPA | 981 |
KCNH4 | L-----RP-----PCLSPCASRPPPSLQDT>T<LAEVH-CPASV--GTMETG--------TAL | 971 |
KCNH5 | H-----ELKEDIQLLSCRMTALEKQVAEIL>K<ILSEKSVPQ--------------------- | 949 |
KCNH6 | Q-----PEGLWP-PLASPLHPLEVQGLICG>-<------------------------------ | 960 |
KCNH7 | T-----DRSFSPSSQCPEFLDLEKSKLKSK>E<SLSSGVHLNTA--SEDNLTSL--------- | 1143 |
KCNH8 | L-----QTGGAAYTQAQLCSSNITSDIWSV>D<PSSVGSSPQRT--GAHEQNPADSELYHSPS | 990 |
CNGA1 | ------------------------------>-<------------------------------ | |
CNGA2 | ------------------------------>-<------------------------------ | |
CNGA3 | ------------------------------>-<------------------------------ | |
CNGA4 | ------------------------------>-<------------------------------ | |
CNGB1 | A-----EPEEHSVRIC-------------->-<------------------------------ | 1226 |
CNGB3 | R-----GTSRQSLIIS-------------->-<------------------------------ | 787 |
HCN1 | --------------VP-QRVTLFRQMSSGA>I<P------PNRGVPPAPP------------- | 861 |
HCN2 | ------------PRLG-P------------>-<----TP-AARAAAPSPD------------- | 862 |
HCN3 | ------------R-LP-PSGLL-------A>K<P------PRTAQPPRPP------------- | 758 |
HCN4 | G-----PPGRPYGAIPGQHVTLPRKTSSGS>L<PPPLSLFGARATSSGGP------------- | 1178 |
cons | > < |
Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
---|---|---|---|---|---|
p.E1119Q | c.3355G>C | Putative Benign | rs199473033 | SIFT: tolerated Polyphen: benign | |
Reports | Putative Benign | Genetic testing for long-QT syndrome: distinguishing pathogenic mutations from benign variants. Circulation. 2009 120(18):1752-60. 19841300 |