No paralogue variants have been mapped to residue 677 for KCNH2.
| KCNH2 | IGSLMYASIFGNVSAIIQRLYSGTARYHTQ>M<LRVREFIRFHQIPNPLRQRLEEYFQHAWSY | 707 |
| KCNH1 | IGSLLYATIFGNVTTIFQQMYANTNRYHEM>L<NSVRDFLKLYQVPKGLSERVMDYIVSTWSM | 546 |
| KCNH3 | IGALMHAVVFGNVTAIIQRMYARRFLYHSR>T<RDLRDYIRIHRIPKPLKQRMLEYFQATWAV | 548 |
| KCNH4 | IGALMHAVVFGNVTAIIQRMYSRRSLYHSR>M<KDLKDFIRVHRLPRPLKQRMLEYFQTTWAV | 522 |
| KCNH5 | VGSLLYATIFGNVTTIFQQMYANTNRYHEM>L<NNVRDFLKLYQVPKGLSERVMDYIVSTWSM | 515 |
| KCNH6 | IGSLMYASIFGNVSAIIQRLYSGTARYHTQ>M<LRVKEFIRFHQIPNPLRQRLEEYFQHAWSY | 559 |
| KCNH7 | IGSLMYASIFGNVSAIIQRLYSGTARYHMQ>M<LRVKEFIRFHQIPNPLRQRLEEYFQHAWTY | 710 |
| KCNH8 | IGALMHALVFGNVTAIIQRMYSRWSLYHTR>T<KDLKDFIRVHHLPQQLKQRMLEYFQTTWSV | 517 |
| CNGA1 | IGVLIFATIVGNIGSMISNMNAARAEFQAR>I<DAIKQYMHFRNVSKDMEKRVIKWFDYLWTN | 444 |
| CNGA2 | IGVLIFATIVGNVGSMISNMNATRAEFQAK>I<DAVKHYMQFRKVSKGMEAKVIRWFDYLWTN | 419 |
| CNGA3 | VGVLIFATIVGNVGSMISNMNASRAEFQAK>I<DSIKQYMQFRKVTKDLETRVIRWFDYLWAN | 447 |
| CNGA4 | LAVMGFATIMGSMSSVIYNMNTADAAFYPD>H<ALVKKYMKLQHVNRKLERRVIDWYQHLQIN | 313 |
| CNGB1 | TGVFAFSVMIGQMRDVVGAATAGQTYYRSC>M<DSTVKYMNFYKIPKSVQNRVKTWYEYTWHS | 927 |
| CNGB3 | SGVFVFSSLIGQMRDVIGAATANQNYFRAC>M<DDTIAYMNNYSIPKLVQKRVRTWYEYTWDS | 489 |
| HCN1 | VGATCYAMFVGHATALIQSLDSSRRQYQEK>Y<KQVEQYMSFHKLPADMRQKIHDYYEHRYQG | 441 |
| HCN2 | VGATCYAMFIGHATALIQSLDSSRRQYQEK>Y<KQVEQYMSFHKLPADFRQKIHDYYEHRYQG | 510 |
| HCN3 | VGATCYAMFIGHATALIQSLDSSRRQYQEK>Y<KQVEQYMSFHKLPADTRQRIHEYYEHRYQG | 394 |
| HCN4 | VGATCYAMFIGHATALIQSLDSSRRQYQEK>Y<KQVEQYMSFHKLPPDTRQRIHDYYEHRYQG | 561 |
| cons | > < |
| Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
|---|---|---|---|---|---|
| p.M677T | c.2030T>C | Putative Benign | SIFT: Polyphen: |