POC5
POC5 centriolar protein
Summary
Involved in centriole elongation and negative regulation of centriole elongation. Located in centriole and centrosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants266 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs3815895 | 5:74,970,024 | T/C | downstream gene variant | — |
| rs1452700301 | 5:74,970,261 | T/C | — | likely benign |
| rs943925494 | 5:74,970,271 | C/T | — | uncertain significance |
| rs371890962 | 5:74,970,293 | G/T | — | likely benign |
| rs1170419775 | 5:74,970,296 | A/C | — | likely benign |
| rs1447488183 | 5:74,970,324 | A/G | — | uncertain significance |
| rs375555924 | 5:74,970,342 | G/A | — | uncertain significance |
| rs2478737444 | 5:74,970,343 | T/C | — | uncertain significance |
| rs896467646 | 5:74,970,347 | A/G | — | likely benign |
| rs768537209 | 5:74,970,355 | G/T | — | uncertain significance |
| rs747754016 | 5:74,970,366 | C/T | — | uncertain significance |
| rs771787338 | 5:74,970,367 | G/A | — | uncertain significance |
| rs550940695 | 5:74,970,372 | T/C | — | uncertain significance |
| rs760243497 | 5:74,970,381 | G/T | — | uncertain significance |
| rs1433562167 | 5:74,970,382 | C/T | — | uncertain significance |
| rs1472451778 | 5:74,970,389 | T/C | — | likely benign |
| rs888897 | 5:74,971,025 | C/T | downstream gene variant | — |
| rs2478756552 | 5:74,973,605 | G/A | — | likely benign |
| rs1775726253 | 5:74,973,613 | G/A | — | uncertain significance |
| rs1408846041 | 5:74,973,621 | T/C | — | uncertain significance |
| rs2478756736 | 5:74,973,629 | A/C | — | likely benign |
| rs2478756800 | 5:74,973,636 | C/T | — | uncertain significance |
| rs1035633933 | 5:74,973,645 | G/A | — | uncertain significance |
| rs771564291 | 5:74,973,646 | G/A | — | uncertain significance |
| rs1208360656 | 5:74,973,659 | T/C | — | uncertain significance |
| rs762351942 | 5:74,973,660 | A/C | — | uncertain significance |
| rs1376783059 | 5:74,973,683 | A/G | — | likely benign |
| rs770294088 | 5:74,973,692 | A/G | — | likely benign |
| rs2478757432 | 5:74,973,701 | A/G | — | likely benign |
| rs146700488 | 5:74,973,716 | C/T | — | likely benign |
| rs751771115 | 5:74,973,717 | C/T | — | uncertain significance |
| rs1411831291 | 5:74,973,722 | T/C | — | likely benign |
| rs2112070713 | 5:74,973,747 | T/G | — | uncertain significance |
| rs1207614486 | 5:74,973,773 | A/G | — | likely benign |
| rs1561459799 | 5:74,973,783 | G/C | — | likely benign |
| rs4703676 | 5:74,979,866 | G/A | — | — |
| rs1776049042 | 5:74,981,013 | C/G | — | likely benign |
| rs760822511 | 5:74,981,051 | G/C | — | uncertain significance |
| rs372819160 | 5:74,981,058 | C/T | — | uncertain significance |
| rs1363942190 | 5:74,981,068 | A/G | — | likely benign |
| rs763910203 | 5:74,981,076 | C/G | — | uncertain significance |
| rs1265821924 | 5:74,981,085 | G/A | — | uncertain significance |
| rs552713438 | 5:74,981,088 | C/T | — | uncertain significance |
| rs376069220 | 5:74,981,089 | G/A | — | likely benign |
| rs34678567 | 5:74,981,103 | C/T | — | conflicting classifications of pathogenicity |
| rs531731919 | 5:74,981,104 | G/A | — | likely benign |
| rs2478797487 | 5:74,981,106 | A/C | — | uncertain significance |
| rs749750536 | 5:74,981,108 | G/A | — | uncertain significance |
| rs774711056 | 5:74,981,116 | G/C | — | likely benign |
| rs772622195 | 5:74,981,119 | A/G | — | likely benign |
| rs377610817 | 5:74,981,129 | G/A | — | uncertain significance |
| rs776606152 | 5:74,981,130 | A/G | — | uncertain significance |
| rs762882160 | 5:74,981,132 | G/T | — | uncertain significance |
| rs965865365 | 5:74,981,140 | G/C | — | likely benign |
| rs199811005 | 5:74,981,145 | C/T | — | uncertain significance |
| rs751576662 | 5:74,981,146 | G/A | — | likely benign |
| rs201773864 | 5:74,981,152 | C/T | — | likely benign |
| rs146984380 | 5:74,981,153 | G/A | — | benign |
| rs201218048 | 5:74,981,154 | C/T | — | uncertain significance |
| rs35898774 | 5:74,981,167 | G/T | — | likely benign |
| rs547644586 | 5:74,981,169 | C/T | — | uncertain significance |
| rs571036542 | 5:74,981,170 | G/T | — | likely benign |
| rs747194599 | 5:74,981,173 | G/A | — | likely benign |
| rs1289410808 | 5:74,981,176 | T/C | — | likely benign |
| rs759525079 | 5:74,981,179 | T/C | — | likely benign |
| rs769986386 | 5:74,981,183 | G/T | — | uncertain significance |
| rs2478798428 | 5:74,981,185 | T/C | — | likely benign |
| rs138072982 | 5:74,981,187 | G/A | — | uncertain significance |
| rs201739662 | 5:74,981,202 | T/C | — | conflicting classifications of pathogenicity |
| rs1234798091 | 5:74,981,206 | T/C | — | likely benign |
| rs200652341 | 5:74,981,208 | G/A | — | uncertain significance |
| rs756722821 | 5:74,981,214 | G/T | — | uncertain significance |
| rs374307702 | 5:74,981,218 | C/A | — | uncertain significance |
| rs368239423 | 5:74,981,219 | G/A | — | uncertain significance |
| rs2478798892 | 5:74,981,225 | G/C | — | uncertain significance |
| rs917512153 | 5:74,981,241 | G/A | — | uncertain significance |
| rs778524728 | 5:74,981,250 | G/A | — | uncertain significance |
| rs778216774 | 5:74,981,276 | T/C | — | uncertain significance |
| rs202094495 | 5:74,981,284 | C/T | — | likely benign |
| rs1221114605 | 5:74,981,295 | T/A | — | uncertain significance |
| rs141696191 | 5:74,981,300 | G/A | — | conflicting classifications of pathogenicity |
| rs769743688 | 5:74,981,304 | C/T | — | uncertain significance |
| rs775658173 | 5:74,981,306 | A/G | — | uncertain significance |
| rs17563610 | 5:74,981,322 | A/T | — | benign |
| rs2478799873 | 5:74,981,325 | T/C | — | likely benign |
| rs16872770 | 5:74,984,619 | G/A | intron variant | — |
| rs17563686 | 5:74,984,818 | A/T | — | benign |
| rs757533955 | 5:74,984,825 | T/C | — | likely benign |
| rs2478817175 | 5:74,984,848 | C/G | — | uncertain significance |
| rs2478817288 | 5:74,984,857 | A/C | — | uncertain significance |
| rs749380864 | 5:74,984,865 | C/A | — | uncertain significance |
| rs773129235 | 5:74,984,889 | T/C | — | likely benign |
| rs746986549 | 5:74,984,891 | C/G | — | uncertain significance |
| rs770607711 | 5:74,984,893 | C/A | — | uncertain significance |
| rs901059127 | 5:74,984,912 | T/A | — | uncertain significance |
| rs559852882 | 5:74,984,914 | A/C | — | uncertain significance |
| rs1307643669 | 5:74,984,936 | T/G | — | uncertain significance |
| rs368789105 | 5:74,984,942 | G/A | — | uncertain significance |
| rs2478818222 | 5:74,984,943 | T/G | — | uncertain significance |
| rs1272894873 | 5:74,984,952 | T/A | — | uncertain significance |
Showing 100 of 266 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.