No paralogue variants have been mapped to residue 668 for KCNH2.
KCNH2 | KIFSICVMLIGSLMYASIFGNVSAIIQRLY>S<GTARYHTQMLRVREFIRFHQIPNPLRQRLE | 698 |
KCNH1 | KIFAVAIMMIGSLLYATIFGNVTTIFQQMY>A<NTNRYHEMLNSVRDFLKLYQVPKGLSERVM | 537 |
KCNH3 | KIFSICTMLIGALMHAVVFGNVTAIIQRMY>A<RRFLYHSRTRDLRDYIRIHRIPKPLKQRML | 539 |
KCNH4 | KIFSICTMLIGALMHAVVFGNVTAIIQRMY>S<RRSLYHSRMKDLKDFIRVHRLPRPLKQRML | 513 |
KCNH5 | KMFSVAMMMVGSLLYATIFGNVTTIFQQMY>A<NTNRYHEMLNNVRDFLKLYQVPKGLSERVM | 506 |
KCNH6 | KVFSICVMLIGSLMYASIFGNVSAIIQRLY>S<GTARYHTQMLRVKEFIRFHQIPNPLRQRLE | 550 |
KCNH7 | KIFSICVMLIGSLMYASIFGNVSAIIQRLY>S<GTARYHMQMLRVKEFIRFHQIPNPLRQRLE | 701 |
KCNH8 | KIFSICTMLIGALMHALVFGNVTAIIQRMY>S<RWSLYHTRTKDLKDFIRVHHLPQQLKQRML | 508 |
CNGA1 | YVFVVVDFLIGVLIFATIVGNIGSMISNMN>A<ARAEFQARIDAIKQYMHFRNVSKDMEKRVI | 435 |
CNGA2 | YLFVIFDFLIGVLIFATIVGNVGSMISNMN>A<TRAEFQAKIDAVKHYMQFRKVSKGMEAKVI | 410 |
CNGA3 | YLFVVVDFLVGVLIFATIVGNVGSMISNMN>A<SRAEFQAKIDSIKQYMQFRKVTKDLETRVI | 438 |
CNGA4 | YLFMVGDFLLAVMGFATIMGSMSSVIYNMN>T<ADAAFYPDHALVKKYMKLQHVNRKLERRVI | 304 |
CNGB1 | IVFQLLNYFTGVFAFSVMIGQMRDVVGAAT>A<GQTYYRSCMDSTVKYMNFYKIPKSVQNRVK | 918 |
CNGB3 | IVFQLLNFFSGVFVFSSLIGQMRDVIGAAT>A<NQNYFRACMDDTIAYMNNYSIPKLVQKRVR | 480 |
HCN1 | LWITMLSMIVGATCYAMFVGHATALIQSLD>S<SRRQYQEKYKQVEQYMSFHKLPADMRQKIH | 432 |
HCN2 | IWLTMLSMIVGATCYAMFIGHATALIQSLD>S<SRRQYQEKYKQVEQYMSFHKLPADFRQKIH | 501 |
HCN3 | VWLTMLSMIVGATCYAMFIGHATALIQSLD>S<SRRQYQEKYKQVEQYMSFHKLPADTRQRIH | 385 |
HCN4 | VWLTMLSMIVGATCYAMFIGHATALIQSLD>S<SRRQYQEKYKQVEQYMSFHKLPPDTRQRIH | 552 |
cons | > < |
Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
---|---|---|---|---|---|
p.S668L | c.2003C>T | Putative Benign | SIFT: Polyphen: |