KCTD19
potassium channel tetramerization domain containing 19
Summary
Predicted to enable identical protein binding activity. Predicted to be involved in male meiotic nuclear division. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants44 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs751192202 | 16:67,323,575 | G/C | — | uncertain significance |
| rs527266432 | 16:67,324,807 | C/T | — | uncertain significance |
| rs1188795135 | 16:67,324,846 | G/T | — | uncertain significance |
| rs200502378 | 16:67,324,886 | G/C | — | uncertain significance |
| rs199535652 | 16:67,325,356 | G/C | — | uncertain significance |
| rs1282940123 | 16:67,325,564 | T/G | — | uncertain significance |
| rs558927777 | 16:67,325,602 | G/A | — | uncertain significance |
| rs1472678469 | 16:67,325,614 | A/G | — | uncertain significance |
| rs73592836 | 16:67,325,679 | G/A | — | benign |
| rs114108483 | 16:67,325,688 | T/C | — | benign |
| rs1429250265 | 16:67,325,735 | G/A | — | uncertain significance |
| rs16957291 | 16:67,326,102 | T/A | downstream gene variant | — |
| rs73592842 | 16:67,327,470 | C/T | — | benign |
| rs1259909819 | 16:67,327,510 | A/T | — | uncertain significance |
| rs200929259 | 16:67,327,690 | G/A | — | uncertain significance |
| rs780973499 | 16:67,327,780 | C/T | — | uncertain significance |
| rs201700190 | 16:67,327,840 | G/A | — | uncertain significance |
| rs769658974 | 16:67,327,935 | C/T | — | uncertain significance |
| rs2036735283 | 16:67,328,002 | G/C | — | uncertain significance |
| rs2036735534 | 16:67,328,017 | T/C | — | uncertain significance |
| rs2507724589 | 16:67,328,487 | T/G | — | uncertain significance |
| rs200312357 | 16:67,328,891 | T/G | — | uncertain significance |
| rs115827904 | 16:67,329,276 | C/T | — | likely benign |
| rs201286450 | 16:67,330,089 | G/A | — | likely benign |
| rs917495926 | 16:67,330,160 | C/T | — | uncertain significance |
| rs1029861628 | 16:67,331,528 | G/A | — | uncertain significance |
| rs9930024 | 16:67,331,854 | T/C | intron variant | — |
| rs556759064 | 16:67,333,323 | G/A | — | uncertain significance |
| rs780820540 | 16:67,333,328 | C/G | — | uncertain significance |
| rs776552397 | 16:67,333,354 | A/G | — | uncertain significance |
| rs548397608 | 16:67,333,425 | C/T | — | uncertain significance |
| rs16957304 | 16:67,334,969 | A/G | intron variant | — |
| rs371354193 | 16:67,337,058 | G/A | — | uncertain significance |
| rs1352596270 | 16:67,337,076 | A/G | — | uncertain significance |
| rs1419186284 | 16:67,337,088 | C/G | — | uncertain significance |
| rs190821373 | 16:67,337,093 | G/A | — | uncertain significance |
| rs2507742729 | 16:67,337,201 | G/C | — | uncertain significance |
| rs752134012 | 16:67,338,371 | C/T | — | uncertain significance |
| rs777260682 | 16:67,338,381 | T/C | — | uncertain significance |
| rs16957311 | 16:67,343,758 | A/C | — | — |
| rs139260482 | 16:67,351,696 | C/T | downstream gene variant | — |
| rs11862222 | 16:67,352,965 | C/G | — | — |
| rs869312866 | 16:67,354,577 | G/T | missense variant | pathogenic |
| rs2507768659 | 16:67,354,705 | G/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.