LINC02210-CRHR1
LINC02210-CRHR1 readthrough
Summary
This locus represents naturally occurring readthrough transcription between neighboring genes CRHR1-IT1, CRHR1 intronic transcript 1 (Gene ID: 147081) and CRHR1, corticotropin releasing hormone receptor 1 (Gene ID: 1394) on chromosome 17. The readthrough transcript encodes a protein that shares sequence identity with the product of the CRHR1 gene. [provided by RefSeq, Dec 2016]
Known Variants66 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs439945 | 17:43,726,659 | A/G | — | — |
| rs241036 | 17:43,731,719 | A/C | intron variant | — |
| rs7214503 | 17:43,739,699 | T/G | intron variant | — |
| rs62053943 | 17:43,744,203 | C/T | intron variant | — |
| rs1724407 | 17:43,747,615 | C/G | — | — |
| rs62055691 | 17:43,754,850 | T/C | intron variant | — |
| rs55974014 | 17:43,757,450 | C/T | — | — |
| rs62055696 | 17:43,758,125 | A/G | intron variant | — |
| rs62055701 | 17:43,758,787 | G/A | intron variant | — |
| rs76539714 | 17:43,758,887 | A/G | intron variant | — |
| rs57222984 | 17:43,758,898 | A/G | intron variant | — |
| rs117849721 | 17:43,763,292 | G/T | intron variant | — |
| rs76761706 | 17:43,776,741 | T/C | intron variant | — |
| rs80143279 | 17:43,776,742 | T/C | intron variant | — |
| rs1724425 | 17:43,781,747 | C/T | intron variant | — |
| rs62056905 | 17:43,782,693 | A/T | — | — |
| rs9912362 | 17:43,784,228 | T/C | intron variant | — |
| rs112123127 | 17:43,785,098 | C/T | intron variant | — |
| rs61667602 | 17:43,785,349 | T/G | — | — |
| rs62056931 | 17:43,789,698 | G/A | intron variant | — |
| rs113100008 | 17:43,789,710 | C/G | intron variant | — |
| rs62056934 | 17:43,790,005 | A/G | intron variant | — |
| rs78803763 | 17:43,791,405 | C/T | — | — |
| rs56406407 | 17:43,792,099 | T/C | intron variant | — |
| rs11655470 | 17:43,795,433 | C/T | intron variant | — |
| rs55938136 | 17:43,798,360 | A/G | intron variant | — |
| rs55896111 | 17:43,799,048 | G/A | intron variant | — |
| rs1358071 | 17:43,803,189 | C/G | — | — |
| rs35116560 | 17:43,804,186 | T/G | — | — |
| rs9303521 | 17:43,805,194 | T/C | — | — |
| rs7225384 | 17:43,809,096 | C/A | coding sequence variant | — |
| rs75022332 | 17:43,810,873 | A/T | coding sequence variant | — |
| rs77804065 | 17:43,810,896 | C/G | — | — |
| rs17563683 | 17:43,811,072 | A/G | upstream gene variant | — |
| rs1880753 | 17:43,811,260 | G/A | regulatory region variant | — |
| rs10451283 | 17:43,814,020 | T/C | upstream gene variant | — |
| rs7220839 | 17:43,815,145 | C/T | upstream gene variant | — |
| rs9906974 | 17:43,822,772 | T/G | — | — |
| rs62054430 | 17:43,823,585 | A/G | regulatory region variant | — |
| rs7207400 | 17:43,824,360 | T/C | intron variant | — |
| rs1880756 | 17:43,826,666 | C/T | intron variant | — |
| rs79172804 | 17:43,828,764 | G/A | intron variant | — |
| rs17426174 | 17:43,830,938 | G/C | intron variant | — |
| rs1880754 | 17:43,833,199 | T/C | intron variant | — |
| rs11079716 | 17:43,834,873 | G/A | intron variant | — |
| rs56214516 | 17:43,836,953 | A/C | intron variant | — |
| rs62055888 | 17:43,838,720 | C/T | intron variant | — |
| rs11079718 | 17:43,839,951 | A/T | intron variant | — |
| rs55657917 | 17:43,844,560 | T/G | intron variant | — |
| rs58089049 | 17:43,845,480 | T/C | regulatory region variant | — |
| rs62055935 | 17:43,848,750 | T/C | intron variant | — |
| rs79730878 | 17:43,849,415 | T/C | intron variant | — |
| rs187045620 | 17:43,849,701 | C/A | intron variant | — |
| rs60814418 | 17:43,850,645 | C/T | regulatory region variant | — |
| rs35909029 | 17:43,851,498 | T/G | — | — |
| rs12953076 | 17:43,854,015 | C/T | intron variant | — |
| rs12938031 | 17:43,854,502 | A/G | intron variant | — |
| rs34186148 | 17:43,854,655 | G/A | — | — |
| rs4076453 | 17:43,855,603 | A/T | — | — |
| rs4076452 | 17:43,855,894 | G/C | intron variant | — |
| rs35076622 | 17:43,856,458 | G/A | intron variant | — |
| rs62057061 | 17:43,856,639 | C/G | intron variant | — |
| rs111433752 | 17:43,857,989 | T/C | — | — |
| rs111664122 | 17:43,857,990 | T/C | upstream gene variant | — |
| rs12942254 | 17:43,858,705 | C/A | upstream gene variant | — |
| rs62057070 | 17:43,859,640 | A/G | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.