NCAPH2
non-SMC condensin II complex subunit H2
Summary
This gene encodes one of the non-SMC subunits of the condensin II complex. This complex plays an essential role in mitotic chromosome assembly. Alternate splicing of this gene results in multiple transcript variants.[provided by RefSeq, May 2010]
Known Variants51 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs543594419 | 22:50,949,811 | T/C | — | — |
| rs150971534 | 22:50,954,928 | T/C | — | uncertain significance |
| rs372044931 | 22:50,956,064 | G/A | — | likely benign |
| rs201599631 | 22:50,956,071 | C/T | — | uncertain significance |
| rs200126237 | 22:50,956,117 | G/A | regulatory region variant | — |
| rs138318301 | 22:50,956,231 | C/T | — | uncertain significance |
| rs2522398978 | 22:50,956,234 | C/T | — | uncertain significance |
| rs200070310 | 22:50,956,420 | C/T | — | uncertain significance |
| rs1268867919 | 22:50,956,460 | A/G | — | uncertain significance |
| rs2522403752 | 22:50,956,623 | C/G | — | uncertain significance |
| rs774544738 | 22:50,956,647 | C/T | — | uncertain significance |
| rs971752138 | 22:50,956,677 | G/C | — | uncertain significance |
| rs369545189 | 22:50,957,083 | G/A | — | likely benign |
| rs750500356 | 22:50,957,104 | A/G | — | uncertain significance |
| rs35126828 | 22:50,957,115 | C/T | — | benign |
| rs574318930 | 22:50,957,116 | G/A | — | uncertain significance |
| rs144020470 | 22:50,957,160 | A/G | — | likely benign |
| rs35941723 | 22:50,957,625 | C/T | — | uncertain significance |
| rs763292905 | 22:50,957,639 | A/C | — | uncertain significance |
| rs2069014294 | 22:50,957,654 | G/A | — | uncertain significance |
| rs553964471 | 22:50,957,714 | G/A | — | likely benign |
| rs141411669 | 22:50,959,425 | G/A | — | uncertain significance |
| rs2522429760 | 22:50,959,436 | G/C | — | uncertain significance |
| rs2522429966 | 22:50,959,451 | G/A | — | uncertain significance |
| rs2148666678 | 22:50,959,984 | C/G | — | uncertain significance |
| rs1292731472 | 22:50,959,991 | A/G | — | uncertain significance |
| rs138253876 | 22:50,960,002 | C/T | — | uncertain significance |
| rs131814 | 22:50,960,101 | G/A | downstream gene variant | — |
| rs138105501 | 22:50,960,191 | C/G | — | uncertain significance |
| rs149386805 | 22:50,960,215 | A/G | — | uncertain significance |
| rs200506211 | 22:50,960,220 | C/T | — | uncertain significance |
| rs753995253 | 22:50,960,245 | T/C | — | uncertain significance |
| rs367983731 | 22:50,960,612 | A/T | — | uncertain significance |
| rs370391598 | 22:50,960,661 | G/A | — | uncertain significance |
| rs113245089 | 22:50,960,791 | G/A | — | benign |
| rs80181807 | 22:50,960,988 | C/T | — | benign |
| rs145541275 | 22:50,960,989 | G/A | — | uncertain significance |
| rs1291168373 | 22:50,961,253 | C/A | — | uncertain significance |
| rs774767027 | 22:50,961,272 | A/G | — | uncertain significance |
| rs760086665 | 22:50,961,273 | G/T | — | uncertain significance |
| rs760990600 | 22:50,961,289 | A/G | — | uncertain significance |
| rs751567124 | 22:50,961,304 | C/T | — | uncertain significance |
| rs760658504 | 22:50,961,459 | C/T | — | uncertain significance |
| rs756864328 | 22:50,961,474 | C/T | — | uncertain significance |
| rs145267080 | 22:50,961,521 | T/C | — | uncertain significance |
| rs373353863 | 22:50,961,543 | C/T | — | uncertain significance |
| rs142305731 | 22:50,961,552 | C/T | — | uncertain significance |
| rs2522459093 | 22:50,961,682 | G/A | — | uncertain significance |
| rs377567490 | 22:50,961,715 | G/A | — | uncertain significance |
| rs1216536521 | 22:50,961,747 | C/G | — | uncertain significance |
| rs370120121 | 22:50,961,752 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.