NKPD1
NTPase KAP family P-loop domain containing 1
Summary
Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants53 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs190994764 | 19:45,652,813 | G/A | downstream gene variant | — |
| rs2513789016 | 19:45,655,233 | A/G | — | likely benign |
| rs1488967404 | 19:45,655,275 | T/G | — | uncertain significance |
| rs775965051 | 19:45,655,294 | C/G | — | uncertain significance |
| rs971778883 | 19:45,655,311 | G/C | — | likely benign |
| rs374022307 | 19:45,655,314 | C/A | — | uncertain significance |
| rs28469095 | 19:45,655,333 | T/C | missense variant | — |
| rs1193123147 | 19:45,655,347 | G/A | — | uncertain significance |
| rs776363032 | 19:45,655,363 | G/A | — | uncertain significance |
| rs2513789810 | 19:45,655,419 | G/T | — | uncertain significance |
| rs937398523 | 19:45,655,433 | C/T | — | uncertain significance |
| rs1482414181 | 19:45,655,543 | G/A | — | uncertain significance |
| rs773272948 | 19:45,655,627 | G/A | — | uncertain significance |
| rs11083761 | 19:45,655,636 | G/A | missense variant | — |
| rs964513287 | 19:45,655,639 | C/T | — | uncertain significance |
| rs528787104 | 19:45,655,737 | G/A | — | uncertain significance |
| rs946021393 | 19:45,655,781 | C/G | — | uncertain significance |
| rs1402699040 | 19:45,655,798 | C/A | — | uncertain significance |
| rs1474683569 | 19:45,655,828 | G/A | — | uncertain significance |
| rs1397799206 | 19:45,655,894 | G/A | — | uncertain significance |
| rs1195789138 | 19:45,655,926 | T/C | — | uncertain significance |
| rs772846447 | 19:45,655,942 | C/T | — | uncertain significance |
| rs761045045 | 19:45,655,992 | C/T | — | uncertain significance |
| rs373185063 | 19:45,656,064 | G/T | — | uncertain significance |
| rs1007090818 | 19:45,656,175 | T/G | — | uncertain significance |
| rs2513792848 | 19:45,656,176 | T/A | — | uncertain significance |
| rs541451013 | 19:45,656,316 | C/T | — | uncertain significance |
| rs2513793608 | 19:45,656,388 | A/G | — | uncertain significance |
| rs2513793736 | 19:45,656,430 | C/T | — | uncertain significance |
| rs573905490 | 19:45,656,545 | C/T | — | uncertain significance |
| rs2513794258 | 19:45,656,556 | A/C | — | uncertain significance |
| rs1465022751 | 19:45,656,641 | C/T | — | uncertain significance |
| rs776706502 | 19:45,656,823 | T/C | — | uncertain significance |
| rs768313896 | 19:45,656,957 | G/T | — | likely benign |
| rs761333255 | 19:45,656,974 | G/A | — | uncertain significance |
| rs764948270 | 19:45,656,977 | A/G | — | uncertain significance |
| rs776354234 | 19:45,661,971 | C/T | — | uncertain significance |
| rs150780522 | 19:45,661,972 | G/A | — | uncertain significance |
| rs758503732 | 19:45,662,013 | G/A | — | uncertain significance |
| rs1968951251 | 19:45,662,037 | C/T | — | uncertain significance |
| rs139188280 | 19:45,662,055 | G/A | — | uncertain significance |
| rs770768260 | 19:45,662,073 | G/A | — | uncertain significance |
| rs188197202 | 19:45,662,215 | C/T | — | likely benign |
| rs1358231793 | 19:45,662,233 | G/A | — | uncertain significance |
| rs375626654 | 19:45,662,247 | C/T | — | uncertain significance |
| rs1568459097 | 19:45,662,254 | C/A | — | uncertain significance |
| rs1968957637 | 19:45,662,262 | C/T | — | uncertain significance |
| rs1276689967 | 19:45,662,281 | A/G | — | uncertain significance |
| rs1473418034 | 19:45,662,299 | G/A | — | uncertain significance |
| rs961793370 | 19:45,662,319 | C/T | — | uncertain significance |
| rs570252134 | 19:45,662,341 | G/A | — | likely benign |
| rs1328341921 | 19:45,663,323 | C/T | — | likely benign |
| rs2513804350 | 19:45,663,354 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.