No paralogue variants have been mapped to residue 977 for KCNH2.
| KCNH2 | RSSSPLRLVPFSSP-RPPGEPPGGEPLMED>C<------------------------------ | 977 |
| KCNH1 | TVRESPATPVSFQA-ASTSGVPDHAKLQAP>G<S----------------------------- | 819 |
| KCNH3 | GRGRPGRAGALKAE-AGPSAPPRALEG--->-<------------------------------ | 806 |
| KCNH4 | SPSLSPALAGQGHS-ASPHGPPRCSAAWKP>P<Q----------------------------- | 809 |
| KCNH5 | TPIQTSLAYVKTSE-SLKQNNRDAMELKPN>G<G----------------------------- | 789 |
| KCNH6 | WPELLQEMPPRHSP-QSPQEDPDCWPLKLG>S<R----------------------------- | 825 |
| KCNH7 | LFSGIVDSSPGIGK-ASGLDFEETVPTSGR>M<H----------------------------- | 978 |
| KCNH8 | SPIRVSRSNSPKTK-QEIDPPNHNKRKEKN>L<K----------------------------- | 795 |
| CNGA1 | ------------------------------>-<------------------------------ | |
| CNGA2 | ------------------------------>-<------------------------------ | |
| CNGA3 | ------------------------------>-<------------------------------ | |
| CNGA4 | E----------------------------->-<------------------------------ | 562 |
| CNGB1 | -------HTHPKEA---------------->-<------------------------------ | 1179 |
| CNGB3 | -------EDKGKE----------------->-<------------------------------ | 736 |
| HCN1 | -------S---------------------->-<------------------------------ | 680 |
| HCN2 | ------------------------------>-<------------------------------ | |
| HCN3 | -------P---------------------->-<------------------------------ | 630 |
| HCN4 | PAAIFRPPPGSGLGNLGAGQTPRHLKRLQS>L<IPSALGSASPASSPSQVDTPSSSSFHIQQL | 862 |
| cons | > < |
| Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
|---|---|---|---|---|---|
| p.C977S | c.2930G>C | Inherited Arrhythmia | LQTS | SIFT: Polyphen: | |
| Reports | Inherited Arrhythmia | LQTS | Genetic characteristics of children and adolescents with long-QT syndrome diagnosed by school-based electrocardiographic screening programs. Circ Arrhythm Electrophysiol. 2014 7(1):107-12. doi: 10.1161/CIRCEP.113.000426. 24363352 | ||
| p.C977F | c.2930G>T | Putative Benign | SIFT: Polyphen: | ||
| p.C977W | c.2931C>G | Putative Benign | SIFT: tolerated Polyphen: benign | ||