NCOA7
nuclear receptor coactivator 7
Summary
Enables nuclear receptor binding activity and transcription coactivator activity. Involved in positive regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants61 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs11154331 | 6:126,111,429 | A/C | — | — |
| rs9398791 | 6:126,115,821 | T/C | regulatory region variant | — |
| rs9375411 | 6:126,116,953 | A/C | — | — |
| rs11967627 | 6:126,122,564 | A/G | intron variant | — |
| rs549438 | 6:126,134,936 | G/A | intron variant | — |
| rs762469052 | 6:126,136,504 | G/A | — | uncertain significance |
| rs779597306 | 6:126,136,532 | A/G | — | uncertain significance |
| rs529858 | 6:126,137,924 | C/A | intron variant | — |
| rs78461345 | 6:126,151,100 | G/A | intron variant | — |
| rs490361 | 6:126,153,253 | T/C | intron variant | — |
| rs9375414 | 6:126,154,475 | G/A | intron variant | — |
| rs17708107 | 6:126,163,599 | A/G | intron variant | — |
| rs6922416 | 6:126,166,867 | C/T | intron variant | — |
| rs777525135 | 6:126,176,309 | C/G | — | uncertain significance |
| rs4895800 | 6:126,178,587 | A/T | — | — |
| rs6920965 | 6:126,179,111 | G/T | — | — |
| rs759941790 | 6:126,196,056 | A/C | — | uncertain significance |
| rs139662554 | 6:126,196,076 | A/G | — | uncertain significance |
| rs2483442681 | 6:126,196,095 | A/G | — | uncertain significance |
| rs779870115 | 6:126,203,593 | G/T | — | uncertain significance |
| rs201538729 | 6:126,206,374 | C/G | — | uncertain significance |
| rs773584572 | 6:126,206,480 | C/G | — | uncertain significance |
| rs191578827 | 6:126,207,917 | A/G | intron variant | — |
| rs754695094 | 6:126,210,187 | C/A | — | uncertain significance |
| rs751145926 | 6:126,210,275 | C/T | — | uncertain significance |
| rs1425665545 | 6:126,210,332 | A/T | — | uncertain significance |
| rs1285101321 | 6:126,210,381 | C/T | — | uncertain significance |
| rs201370198 | 6:126,210,390 | C/A | — | uncertain significance |
| rs2483557666 | 6:126,210,392 | T/C | — | uncertain significance |
| rs2483558344 | 6:126,210,434 | G/A | — | uncertain significance |
| rs377026001 | 6:126,210,540 | G/A | — | uncertain significance |
| rs745673617 | 6:126,210,705 | C/T | — | uncertain significance |
| rs144077211 | 6:126,210,706 | G/A | — | likely benign |
| rs774715567 | 6:126,210,741 | A/G | — | uncertain significance |
| rs1784485965 | 6:126,210,746 | G/A | — | uncertain significance |
| rs1164852139 | 6:126,210,813 | A/C | — | uncertain significance |
| rs2483564173 | 6:126,210,825 | A/T | — | uncertain significance |
| rs139109113 | 6:126,210,833 | T/A | — | uncertain significance |
| rs144006908 | 6:126,210,846 | A/G | — | uncertain significance |
| rs569408777 | 6:126,210,900 | C/T | — | uncertain significance |
| rs150951617 | 6:126,210,936 | A/G | — | uncertain significance |
| rs781108701 | 6:126,210,940 | G/C | — | uncertain significance |
| rs770648833 | 6:126,210,969 | C/T | — | uncertain significance |
| rs1432327126 | 6:126,210,987 | C/T | — | uncertain significance |
| rs371248704 | 6:126,211,045 | C/G | — | uncertain significance |
| rs376913669 | 6:126,211,907 | G/A | — | uncertain significance |
| rs558713338 | 6:126,211,949 | C/T | — | uncertain significance |
| rs1784571071 | 6:126,211,952 | G/C | — | uncertain significance |
| rs11154334 | 6:126,214,624 | A/C | intron variant | — |
| rs9385389 | 6:126,215,486 | G/A | — | — |
| rs376310829 | 6:126,236,519 | G/A | — | uncertain significance |
| rs746237943 | 6:126,242,098 | G/A | — | uncertain significance |
| rs146432117 | 6:126,242,152 | G/A | — | uncertain significance |
| rs776045538 | 6:126,242,167 | G/A | — | likely benign |
| rs373968472 | 6:126,243,832 | C/G | — | uncertain significance |
| rs748644195 | 6:126,243,850 | G/C | — | uncertain significance |
| rs764131356 | 6:126,243,921 | C/T | — | uncertain significance |
| rs770933002 | 6:126,249,790 | T/C | — | uncertain significance |
| rs2483867710 | 6:126,249,855 | G/A | — | uncertain significance |
| rs779584932 | 6:126,249,900 | G/T | — | uncertain significance |
| rs1567 | 6:126,249,914 | T/G | missense variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.