No paralogue variants have been mapped to residue 1098 for KCNH2.
KCNH2 | ------------GPGPTSTSPLL-----PV>S<PLP-TLTLDSLSQVSQFMACEELPPGAPEL | 1127 |
KCNH1 | ------YPIPEQTLQATVLEVRH-----EL>K<EDIKALNAKMTNIEKQLSEILRILTSRRS- | 963 |
KCNH3 | -----CPRAS-----GEGPCPASTSGLLQP>L<CVDTGASSYCLQPPAGSVLSGTWPHPRPGP | 968 |
KCNH4 | ------GHPAGSAWTPDPPCPQL-----RP>-<----PCLSPCASRPPPSLQDTTLAEVH-CP | 959 |
KCNH5 | ------YPIPEQALQTTLQEVKH-----EL>K<EDIQLLSCRMTALEKQVAEILKILSEKSVP | 948 |
KCNH6 | ------------KTLAPSSEQEQ-----PE>G<LWP-PLASPLHPLEVQGLICG--------- | 960 |
KCNH7 | ------PIIQLMRTSQPEASIKT-----DR>S<FSPSSQCPEFLDLEKSKLKSKESLSSGVHL | 1132 |
KCNH8 | VCPSRESLQTRTSWSAHQPCLHL-----QT>G<GAAYTQAQLCSSNITSDIWSVDPSSVGSSP | 970 |
CNGA1 | ------------------------------>-<------------------------------ | |
CNGA2 | ------------------------------>-<------------------------------ | |
CNGA3 | ------------------------------>-<------------------------------ | |
CNGA4 | ------------------------------>-<------------------------------ | |
CNGB1 | -----------LGRPEGEEEGPA-----EP>E<EHSVRIC----------------------- | 1226 |
CNGB3 | -----------VRR----TVLPR-----GT>S<RQSLIIS----------------------- | 787 |
HCN1 | ---------AG----G---RST-------->-<-----VP-QRVTLFRQMSSGAIP------P | 852 |
HCN2 | ---------------S---ST--------->-<---PRLG-P-----------------TP-A | 853 |
HCN3 | ---------------G---SE--------->-<---R-LP-PSGLL-------AKP------P | 749 |
HCN4 | ---------------S---GGLG-----PP>G<RPYGAIPGQHVTLPRKTSSGSLPPPLSLFG | 1169 |
cons | > < |
Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
---|---|---|---|---|---|
p.S1098R | c.3292A>C | Putative Benign | SIFT: tolerated Polyphen: benign |