| Paralogue | Variant | Associated Disease | Mapping Quality | Consensus | Pubmed |
|---|---|---|---|---|---|
| KCNQ2 | R207Q | Peripheral nerve hyperexcitability | High | 9 | 17872363, 22455920 |
| KCNQ2 | R207W | Epilepsy, benign neonatal | High | 9 | 11572947, 22455920 |
| KCNC3 | R423H | Spinocerebellar ataxia 13 | High | 9 | 19953606, 22289912, 23734863, 25756792, 26795593 |
| KCNC1 | R320H | Epilepsy, progressive myoclonus | High | 9 | 25401298, 25401298 |
| KCNB1 | R306C | Epilepsy, infantile | High | 9 | 26477325 |
To assess whether the paralogue annotation here confidently predicts that variation at this residue is pathogenic, it is important to check the reports in the Pubmed links above to ascertain that the mutations in these paralogues have been proved likely to be disease-causing. It is also important to check that the direction of effect of the variant in the paralogue is compatible with your observed phenotype in KCNQ1.
| KCNQ1 | ----------SKGQVFATSAIRGIRFLQIL>R<MLHVDRQGGTWRLLGSVVFIHRQELITTLY | 267 |
| KCNQ2 | ----------SQGNVFATSALRSLRFLQIL>R<MIRMDRRGGTWKLLGSVVYAHSKELVTAWY | 237 |
| KCNQ3 | ----------NQGNVLA-TSLRSLRFLQIL>R<MLRMDRRGGTWKLLGSAICAHSKELITAWY | 266 |
| KCNQ4 | ----------TQGNIFATSALRSMRFLQIL>R<MVRMDRRGGTWKLLGSVVYAHSKELITAWY | 243 |
| KCNQ5 | ----------TQGNIFATSALRSLRFLQIL>R<MVRMDRRGGTWKLLGSVVYAHSKELITAWY | 271 |
| KCNA1 | -------N-QKGEQATSLAILRVIRLVRVF>R<IFKLSRHSKGLQILGQTLKASMRELGLLIF | 331 |
| KCNA10 | P---------SAQQNMSLAILRIIRLVRVF>R<IFKLSRHSKGLQILGQTLKASMRELGLLIF | 380 |
| KCNA2 | -------DAQQGQQAMSLAILRVIRLVRVF>R<IFKLSRHSKGLQILGQTLKASMRELGLLIF | 333 |
| KCNA3 | ---------GNGQQAMSLAILRVIRLVRVF>R<IFKLSRHSKGLQILGQTLKASMRELGLLIF | 403 |
| KCNA4 | G------GNGQQQQAMSFAILRIIRLVRVF>R<IFKLSRHSKGLQILGHTLRASMRELGLLIF | 483 |
| KCNA5 | --PGGGGGGQNGQQAMSLAILRVIRLVRVF>R<IFKLSRHSKGLQILGKTLQASMRELGLLIF | 439 |
| KCNA6 | QQPASGGGGQNGQQAMSLAILRVIRLVRVF>R<IFKLSRHSKGLQILGKTLQASMRELGLLIF | 381 |
| KCNA7 | ---------GVGQQAMSLAILRVIRLVRVF>R<IFKLSRHSKGLQILGQTLRASMRELGLLIF | 317 |
| KCNB1 | --------KSVLQFQNVRRVVQIFRIMRIL>R<ILKLARHSTGLQSLGFTLRRSYNELGLLIL | 336 |
| KCNB2 | --------KSVLQFQNVRRVVQIFRIMRIL>R<ILKLARHSTGLQSLGFTLRRSYNELGLLIL | 340 |
| KCNC1 | --------LSSKAAKDVLGFLRVVRFVRIL>R<IFKLTRHFVGLRVLGHTLRASTNEFLLLII | 350 |
| KCNC2 | --------LSSKAAKDVLGFLRVVRFVRIL>R<IFKLTRHFVGLRVLGHTLRASTNEFLLLII | 387 |
| KCNC3 | --------LSSKAAKDVLGFLRVVRFVRIL>R<IFKLTRHFVGLRVLGHTLRASTNEFLLLII | 453 |
| KCNC4 | --------LSSKAARDVLGFLRVVRFVRIL>R<IFKLTRHFVGLRVLGHTLRASTNEFLLLII | 386 |
| KCND1 | ------------KNDDVSGAFVTLRVFRVF>R<IFKFSRHSQGLRILGYTLKSCASELGFLLF | 331 |
| KCND2 | ------------DNEDVSGAFVTLRVFRVF>R<IFKFSRHSQGLRILGYTLKSCASELGFLLF | 329 |
| KCND3 | ------------NNEDVSGAFVTLRVFRVF>R<IFKFSRHSQGLRILGYTLKSCASELGFLLF | 326 |
| KCNF1 | -------GARMMELTNVQQAVQALRIMRIA>R<IFKLARHSSGLQTLTYALKRSFKELGLLLM | 329 |
| KCNG1 | R----KPGAGNSYLDKVGLVLRVLRALRIL>Y<VMRLARHSLGLQTLGLTARRCTREFGLLLL | 382 |
| KCNG2 | A----AGPGGTKLLERAGLVLRLLRALRVL>Y<VMRLARHSLGLRSLGLTMRRCAREFGLLLL | 327 |
| KCNG3 | ------FTGENSQLQRAGVTLRVLRMMRIF>W<VIKLARHFIGLQTLGLTLKRCYREMVMLLV | 328 |
| KCNG4 | G----ERPSGSSYLEKVGLVLRVLRALRIL>Y<VMRLARHSLGLQTLGLTVRRCTREFGLLLL | 376 |
| KCNS1 | --------QGGKEFGHLGKVVQVFRLMRIF>R<VLKLARHSTGLRSLGATLKHSYREVGILLL | 381 |
| KCNS2 | --------ESTPTLANLGRVAQVLRLMRIF>R<ILKLARHSTGLRSLGATLKYSYKEVGLLLL | 334 |
| KCNS3 | --------EESEDIENMGKVVQILRLMRIF>R<ILKLARHSVGLRSLGATLRHSYHEVGLLLL | 329 |
| KCNV1 | --------QTTQELENVGRIVQVLRLLRAL>R<MLKLGRHSTGLRSLGMTITQCYEEVGLLLL | 351 |
| KCNV2 | H----QRGQTVGSVGKVGQVLRVMRLMRIF>R<ILKLARHSTGLRAFGFTLRQCYQQVGCLLL | 416 |
| cons | > < |
There are currently no reported variants at residue 237 for KCNQ1.