GSE1
Gse1 coiled-coil protein
Summary
This gene encodes a proline-rich protein with coiled coil domains that may be a subunit of a BRAF35-HDAC (BHC) histone deacetylase complex. This gene may function as an oncogene in breast cancer and enhanced expression of the encoded protein has been observed in breast cancer patients. [provided by RefSeq, May 2017]
Known Variants208 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7198287 | 16:85,258,191 | C/T | intergenic variant | — |
| rs16975388 | 16:85,261,963 | C/T | — | — |
| rs12598694 | 16:85,264,733 | T/A | — | — |
| rs4258599 | 16:85,293,483 | T/C | intergenic variant | — |
| rs773179297 | 16:85,336,811 | G/A | — | — |
| rs10871292 | 16:85,364,098 | T/G | — | — |
| rs112485629 | 16:85,375,675 | C/T | intergenic variant | — |
| rs4783183 | 16:85,415,465 | C/T | — | — |
| rs4783185 | 16:85,415,626 | A/C | — | — |
| rs729115 | 16:85,416,215 | A/C | — | — |
| rs202099642 | 16:85,443,270 | A/G | — | — |
| rs146442523 | 16:85,443,989 | T/G | intergenic variant | — |
| rs112776824 | 16:85,446,406 | G/C | intergenic variant | — |
| rs534448891 | 16:85,447,173 | C/T | — | — |
| rs189060489 | 16:85,541,801 | A/G | intergenic variant | — |
| rs183401583 | 16:85,595,360 | G/C | regulatory region variant | — |
| rs4240810 | 16:85,625,127 | G/T | upstream gene variant | — |
| rs139489600 | 16:85,637,632 | T/C | intergenic variant | — |
| rs2510697128 | 16:85,667,524 | G/C | — | uncertain significance |
| rs150719571 | 16:85,667,528 | C/T | — | uncertain significance |
| rs202054304 | 16:85,667,558 | C/T | — | uncertain significance |
| rs140144665 | 16:85,667,567 | G/A | — | uncertain significance |
| rs143822889 | 16:85,667,568 | C/T | — | uncertain significance |
| rs1160280190 | 16:85,667,583 | C/T | — | uncertain significance |
| rs773470396 | 16:85,667,594 | C/T | — | uncertain significance |
| rs766447038 | 16:85,667,600 | A/C | — | uncertain significance |
| rs148537143 | 16:85,667,616 | A/G | — | uncertain significance |
| rs1201882241 | 16:85,667,621 | G/A | — | uncertain significance |
| rs2510700100 | 16:85,667,649 | C/G | — | uncertain significance |
| rs141419803 | 16:85,667,656 | C/T | — | likely benign |
| rs556048268 | 16:85,667,664 | C/T | — | uncertain significance |
| rs200168352 | 16:85,667,683 | C/T | — | likely benign |
| rs540734949 | 16:85,667,700 | C/T | — | uncertain significance |
| rs8056655 | 16:85,681,437 | T/A | — | — |
| rs776541218 | 16:85,682,217 | C/T | — | uncertain significance |
| rs138417000 | 16:85,682,259 | G/A | — | uncertain significance |
| rs137897923 | 16:85,682,335 | T/G | — | uncertain significance |
| rs779863020 | 16:85,682,352 | C/T | — | uncertain significance |
| rs200326373 | 16:85,687,906 | G/T | — | uncertain significance |
| rs368266182 | 16:85,687,920 | C/T | — | uncertain significance |
| rs763667626 | 16:85,687,935 | C/T | — | uncertain significance |
| rs756826959 | 16:85,687,939 | C/T | — | uncertain significance |
| rs772275707 | 16:85,687,962 | G/A | — | uncertain significance |
| rs373938537 | 16:85,687,974 | C/G | — | uncertain significance |
| rs200380779 | 16:85,687,982 | C/G | — | uncertain significance |
| rs373051722 | 16:85,688,001 | C/G | — | uncertain significance |
| rs1178453116 | 16:85,688,002 | C/T | — | uncertain significance |
| rs201281892 | 16:85,688,007 | G/A | — | uncertain significance |
| rs1430348750 | 16:85,688,008 | G/T | — | uncertain significance |
| rs150879827 | 16:85,688,010 | C/G | — | uncertain significance |
| rs374528847 | 16:85,688,041 | G/A | — | uncertain significance |
| rs1225801343 | 16:85,688,407 | C/T | — | uncertain significance |
| rs150017852 | 16:85,688,434 | A/C | — | uncertain significance |
| rs748812457 | 16:85,688,438 | C/T | — | uncertain significance |
| rs1343538488 | 16:85,688,447 | A/T | — | uncertain significance |
| rs147629403 | 16:85,688,481 | C/T | — | likely benign |
| rs371546617 | 16:85,688,495 | G/A | — | uncertain significance |
| rs142161580 | 16:85,688,513 | C/T | — | uncertain significance |
| rs778445212 | 16:85,688,528 | C/T | — | uncertain significance |
| rs150332530 | 16:85,688,581 | C/G | — | uncertain significance |
| rs372427431 | 16:85,688,584 | C/A | — | uncertain significance |
| rs151194801 | 16:85,689,333 | A/T | — | conflicting classifications of pathogenicity |
| rs370359409 | 16:85,689,339 | G/A | — | uncertain significance |
| rs201346187 | 16:85,689,367 | C/T | — | uncertain significance |
| rs771431123 | 16:85,689,374 | C/A | — | uncertain significance |
| rs763499632 | 16:85,689,421 | C/T | — | uncertain significance |
| rs1342899241 | 16:85,689,453 | C/T | — | uncertain significance |
| rs2051880184 | 16:85,689,471 | T/G | — | uncertain significance |
| rs753968275 | 16:85,689,486 | C/G | — | uncertain significance |
| rs140823421 | 16:85,689,499 | G/A | — | uncertain significance |
| rs114262780 | 16:85,689,510 | C/T | — | benign |
| rs553502127 | 16:85,689,515 | C/A | — | uncertain significance |
| rs199993964 | 16:85,689,517 | C/T | — | uncertain significance |
| rs529768614 | 16:85,689,961 | C/G | — | uncertain significance |
| rs376448790 | 16:85,689,987 | G/A | — | uncertain significance |
| rs369286648 | 16:85,689,988 | C/T | — | likely benign |
| rs201842430 | 16:85,689,998 | C/T | — | uncertain significance |
| rs377678624 | 16:85,690,005 | G/A | — | uncertain significance |
| rs199961563 | 16:85,690,010 | C/T | — | uncertain significance |
| rs376914656 | 16:85,690,024 | C/G | — | likely benign |
| rs764801903 | 16:85,690,025 | G/A | — | uncertain significance |
| rs776522718 | 16:85,690,047 | G/A | — | uncertain significance |
| rs1472944476 | 16:85,690,049 | G/A | — | uncertain significance |
| rs775350316 | 16:85,690,055 | G/A | — | uncertain significance |
| rs766824797 | 16:85,690,064 | C/T | — | uncertain significance |
| rs763744691 | 16:85,690,065 | G/A | — | uncertain significance |
| rs755389489 | 16:85,690,083 | G/A | — | uncertain significance |
| rs754214628 | 16:85,690,107 | G/A | — | uncertain significance |
| rs551844911 | 16:85,690,108 | C/T | — | likely benign |
| rs980636681 | 16:85,690,109 | G/A | — | uncertain significance |
| rs932869228 | 16:85,690,133 | C/T | — | uncertain significance |
| rs766892362 | 16:85,690,134 | G/A | — | uncertain significance |
| rs759866697 | 16:85,690,139 | C/T | — | uncertain significance |
| rs994666153 | 16:85,690,146 | A/C | — | uncertain significance |
| rs1312715811 | 16:85,690,155 | T/C | — | uncertain significance |
| rs748207039 | 16:85,690,160 | G/T | — | uncertain significance |
| rs942636948 | 16:85,690,163 | A/G | — | uncertain significance |
| rs1453548972 | 16:85,690,173 | A/G | — | uncertain significance |
| rs977850231 | 16:85,690,190 | G/A | — | uncertain significance |
| rs371328519 | 16:85,690,195 | C/T | — | likely benign |
Showing 100 of 208 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.