PADI4
peptidyl arginine deiminase 4
Summary
This gene is a member of a gene family which encodes enzymes responsible for the conversion of arginine residues to citrulline residues. This gene may play a role in granulocyte and macrophage development leading to inflammation and immune response. [provided by RefSeq, Jul 2008]
Known Variants76 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1557787212 | 1:17,484,166 | G/T | — | association |
| rs2501796 | 1:17,633,522 | G/A | upstream gene variant | — |
| rs2477134 | 1:17,633,572 | G/T | upstream gene variant | — |
| rs141280036 | 1:17,634,718 | A/G | missense variant | — |
| rs35381732 | 1:17,634,740 | G/A | — | benign |
| rs370820749 | 1:17,634,764 | A/G | — | uncertain significance |
| rs371193672 | 1:17,634,769 | G/A | — | uncertain significance |
| rs34470277 | 1:17,643,054 | G/A | intron variant | — |
| rs11203358 | 1:17,650,247 | A/G | intron variant | — |
| rs757370203 | 1:17,657,519 | G/A | — | uncertain significance |
| rs11203366 | 1:17,657,534 | G/A | missense variant | association |
| rs772051391 | 1:17,657,591 | G/T | — | likely benign |
| rs57969340 | 1:17,657,592 | T/C | — | benign |
| rs35809521 | 1:17,657,607 | C/T | — | benign |
| rs11203367 | 1:17,657,616 | T/C | missense variant | association |
| rs6698443 | 1:17,658,564 | C/A | — | — |
| rs1170553721 | 1:17,660,456 | G/A | — | uncertain significance |
| rs138247576 | 1:17,660,474 | G/A | — | uncertain significance |
| rs144397490 | 1:17,660,490 | A/G | — | uncertain significance |
| rs141897176 | 1:17,660,497 | C/T | — | likely benign |
| rs874881 | 1:17,660,499 | G/T | missense variant | association |
| rs1748035 | 1:17,661,996 | T/A | — | — |
| rs2240340 | 1:17,662,639 | T/C | regulatory region variant | association |
| rs1748033 | 1:17,662,662 | T/C | synonymous variant | association |
| rs1352655534 | 1:17,662,671 | G/A | — | uncertain significance |
| rs571787244 | 1:17,662,684 | C/A | — | uncertain significance |
| rs12733102 | 1:17,662,705 | G/C | missense variant | — |
| rs200387282 | 1:17,662,708 | C/T | — | uncertain significance |
| rs1621005 | 1:17,662,751 | C/G | regulatory region variant | — |
| rs1748031 | 1:17,662,907 | A/G | — | — |
| rs371334403 | 1:17,664,563 | G/A | — | uncertain significance |
| rs779399204 | 1:17,664,580 | G/T | — | likely benign |
| rs11588132 | 1:17,664,615 | T/C | — | benign |
| rs200898889 | 1:17,664,616 | G/A | — | uncertain significance |
| rs111275753 | 1:17,664,622 | C/T | — | benign |
| rs2428736 | 1:17,665,091 | G/A | intron variant | — |
| rs1635579 | 1:17,665,401 | G/A | intron variant | — |
| rs745676601 | 1:17,666,216 | C/T | — | uncertain significance |
| rs142590988 | 1:17,666,222 | C/A | — | likely benign |
| rs147414271 | 1:17,666,263 | G/A | — | likely benign |
| rs773389520 | 1:17,668,476 | C/A | — | uncertain significance |
| rs16825565 | 1:17,668,508 | C/T | — | benign |
| rs35903413 | 1:17,668,563 | A/G | — | benign |
| rs41265997 | 1:17,668,606 | C/G | missense variant | — |
| rs143220365 | 1:17,668,827 | G/A | — | uncertain significance |
| rs113714693 | 1:17,668,840 | T/C | — | benign |
| rs765222511 | 1:17,668,844 | G/A | — | likely benign |
| rs758604276 | 1:17,668,851 | A/T | — | uncertain significance |
| rs756513098 | 1:17,668,883 | G/T | — | uncertain significance |
| rs33981382 | 1:17,668,888 | A/G | missense variant | benign |
| rs774505663 | 1:17,672,609 | A/C | — | uncertain significance |
| rs753015063 | 1:17,672,616 | G/T | — | uncertain significance |
| rs41266003 | 1:17,672,642 | T/C | — | benign |
| rs2301888 | 1:17,672,730 | G/A | intron variant | — |
| rs2240339 | 1:17,674,108 | C/A | — | — |
| rs2240338 | 1:17,674,185 | C/T | intron variant | — |
| rs2240337 | 1:17,674,222 | C/T | intron variant | — |
| rs765542991 | 1:17,674,527 | C/G | — | uncertain significance |
| rs1220280898 | 1:17,674,536 | G/A | — | uncertain significance |
| rs2240335 | 1:17,674,537 | C/A | synonymous variant | benign |
| rs61766763 | 1:17,677,652 | T/G | — | — |
| rs138375185 | 1:17,681,096 | G/A | — | likely benign |
| rs2526097460 | 1:17,681,153 | G/T | — | uncertain significance |
| rs772704328 | 1:17,681,163 | G/A | — | uncertain significance |
| rs776201419 | 1:17,681,178 | C/G | — | uncertain significance |
| rs1456388353 | 1:17,682,488 | C/T | — | uncertain significance |
| rs769216858 | 1:17,682,491 | C/A | — | uncertain significance |
| rs139459202 | 1:17,682,519 | T/G | — | uncertain significance |
| rs10437048 | 1:17,682,719 | A/C | — | — |
| rs531113425 | 1:17,685,793 | C/T | — | uncertain significance |
| rs757040018 | 1:17,685,808 | C/T | — | uncertain significance |
| rs368756799 | 1:17,690,080 | G/A | — | uncertain significance |
| rs142092052 | 1:17,690,083 | C/T | — | likely benign |
| rs201235053 | 1:17,690,084 | G/A | — | uncertain significance |
| rs2526146021 | 1:17,690,196 | C/T | — | likely benign |
| rs368700849 | 1:17,690,210 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.