No paralogue variants have been mapped to residue 698 for KCNH2.
KCNH2 | SGTARYHTQMLRVREFIRFHQIPNPLRQRL>E<EYFQHAWSYTNGIDMNAVLKGFPECLQADI | 728 |
KCNH1 | ANTNRYHEMLNSVRDFLKLYQVPKGLSERV>M<DYIVSTWSMSRGIDTEKVLQICPKDMRADI | 567 |
KCNH3 | ARRFLYHSRTRDLRDYIRIHRIPKPLKQRM>L<EYFQATWAVNNGIDTTELLQSLPDELRADI | 569 |
KCNH4 | SRRSLYHSRMKDLKDFIRVHRLPRPLKQRM>L<EYFQTTWAVNSGIDANELLRDFPDELRADI | 543 |
KCNH5 | ANTNRYHEMLNNVRDFLKLYQVPKGLSERV>M<DYIVSTWSMSKGIDTEKVLSICPKDMRADI | 536 |
KCNH6 | SGTARYHTQMLRVKEFIRFHQIPNPLRQRL>E<EYFQHAWSYTNGIDMNAVLKGFPECLQADI | 580 |
KCNH7 | SGTARYHMQMLRVKEFIRFHQIPNPLRQRL>E<EYFQHAWTYTNGIDMNMVLKGFPECLQADI | 731 |
KCNH8 | SRWSLYHTRTKDLKDFIRVHHLPQQLKQRM>L<EYFQTTWSVNNGIDSNELLKDFPDELRSDI | 538 |
CNGA1 | AARAEFQARIDAIKQYMHFRNVSKDMEKRV>I<KWFDYLWTNKKTVDEKEVLKYLPDKLRAEI | 465 |
CNGA2 | ATRAEFQAKIDAVKHYMQFRKVSKGMEAKV>I<RWFDYLWTNKKTVDEREILKNLPAKLRAEI | 440 |
CNGA3 | ASRAEFQAKIDSIKQYMQFRKVTKDLETRV>I<RWFDYLWANKKTVDEKEVLKSLPDKLKAEI | 468 |
CNGA4 | TADAAFYPDHALVKKYMKLQHVNRKLERRV>I<DWYQHLQINKKMTNEVAILQHLPERLRAEV | 334 |
CNGB1 | AGQTYYRSCMDSTVKYMNFYKIPKSVQNRV>K<TWYEYTWHSQGMLDESELMVQLPDKMRLDL | 948 |
CNGB3 | ANQNYFRACMDDTIAYMNNYSIPKLVQKRV>R<TWYEYTWDSQRMLDESDLLKTLPTTVQLAL | 510 |
HCN1 | SSRRQYQEKYKQVEQYMSFHKLPADMRQKI>H<DYYEHRYQG-KIFDEENILNELNDPLREEI | 461 |
HCN2 | SSRRQYQEKYKQVEQYMSFHKLPADFRQKI>H<DYYEHRYQG-KMFDEDSILGELNGPLREEI | 530 |
HCN3 | SSRRQYQEKYKQVEQYMSFHKLPADTRQRI>H<EYYEHRYQG-KMFDEESILGELSEPLREEI | 414 |
HCN4 | SSRRQYQEKYKQVEQYMSFHKLPPDTRQRI>H<DYYEHRYQG-KMFDEESILGELSEPLREEI | 581 |
cons | > < |
Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
---|---|---|---|---|---|
p.E698K | c.2092G>A | Putative Benign | SIFT: Polyphen: |