USF3
upstream transcription factor family member 3
Summary
This gene encodes a large protein that contains a helix-loop-helix domain and a polyglutamine region. A deletion in the polyglutamine region was associated with risk for thyroid carcinoma. [provided by RefSeq, May 2017]
Known Variants109 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1026364 | 3:113,370,010 | G/T | 3 prime UTR variant | benign |
| rs1947328626 | 3:113,373,891 | A/G | — | uncertain significance |
| rs760343877 | 3:113,374,004 | C/A | — | uncertain significance |
| rs753865249 | 3:113,374,129 | T/C | — | uncertain significance |
| rs2549651330 | 3:113,374,139 | A/C | — | uncertain significance |
| rs2549651345 | 3:113,374,171 | T/C | — | uncertain significance |
| rs2549651373 | 3:113,374,203 | G/A | — | uncertain significance |
| rs2549651600 | 3:113,374,350 | G/A | — | uncertain significance |
| rs371204248 | 3:113,374,374 | G/A | — | uncertain significance |
| rs74980526 | 3:113,374,409 | G/A | — | uncertain significance |
| rs377319556 | 3:113,374,413 | C/G | — | uncertain significance |
| rs542739936 | 3:113,374,428 | C/T | — | uncertain significance |
| rs373643148 | 3:113,374,431 | T/C | — | uncertain significance |
| rs778471296 | 3:113,374,453 | G/A | — | uncertain significance |
| rs763049108 | 3:113,374,485 | G/A | — | uncertain significance |
| rs776587053 | 3:113,374,557 | C/T | — | uncertain significance |
| rs184254184 | 3:113,374,627 | G/A | — | conflicting classifications of pathogenicity |
| rs771489545 | 3:113,374,767 | T/C | — | uncertain significance |
| rs756126359 | 3:113,374,788 | T/C | — | uncertain significance |
| rs143667618 | 3:113,374,812 | A/G | — | likely benign |
| rs753880777 | 3:113,374,932 | T/C | — | uncertain significance |
| rs774802687 | 3:113,374,971 | G/A | — | uncertain significance |
| rs760448023 | 3:113,375,110 | G/A | — | uncertain significance |
| rs1256027090 | 3:113,375,125 | T/C | — | uncertain significance |
| rs201006777 | 3:113,375,166 | C/T | — | uncertain significance |
| rs769775764 | 3:113,375,202 | C/T | — | uncertain significance |
| rs775426102 | 3:113,375,219 | C/T | — | conflicting classifications of pathogenicity |
| rs181199143 | 3:113,375,226 | C/T | — | uncertain significance |
| rs571513442 | 3:113,375,250 | A/C | — | uncertain significance |
| rs186056495 | 3:113,375,251 | T/C | — | conflicting classifications of pathogenicity |
| rs375894424 | 3:113,375,257 | T/C | — | uncertain significance |
| rs2549652727 | 3:113,375,280 | A/G | — | uncertain significance |
| rs1231023208 | 3:113,375,362 | G/A | — | uncertain significance |
| rs779904525 | 3:113,375,431 | T/C | — | uncertain significance |
| rs775640044 | 3:113,375,665 | A/T | — | uncertain significance |
| rs1377685600 | 3:113,375,683 | C/G | — | uncertain significance |
| rs1035196852 | 3:113,375,731 | T/C | — | uncertain significance |
| rs756960091 | 3:113,375,854 | G/T | — | uncertain significance |
| rs748185621 | 3:113,375,883 | C/T | — | uncertain significance |
| rs78661215 | 3:113,375,887 | A/G | — | uncertain significance |
| rs780120777 | 3:113,376,000 | T/C | — | uncertain significance |
| rs758523261 | 3:113,376,064 | A/G | — | uncertain significance |
| rs202124437 | 3:113,376,159 | T/A | — | uncertain significance |
| rs182171997 | 3:113,376,202 | G/C | — | uncertain significance |
| rs2549653886 | 3:113,376,228 | G/A | — | uncertain significance |
| rs746826491 | 3:113,376,272 | C/A | — | uncertain significance |
| rs369820220 | 3:113,376,279 | T/C | — | uncertain significance |
| rs2549654116 | 3:113,376,436 | C/A | — | uncertain significance |
| rs1215942730 | 3:113,376,553 | C/A | — | uncertain significance |
| rs769248134 | 3:113,376,684 | T/C | — | uncertain significance |
| rs775058911 | 3:113,376,690 | C/T | — | uncertain significance |
| rs577276138 | 3:113,376,742 | T/C | — | uncertain significance |
| rs765316202 | 3:113,376,756 | G/A | — | uncertain significance |
| rs764697372 | 3:113,376,767 | C/T | — | likely benign |
| rs1421374895 | 3:113,376,841 | T/C | — | likely benign |
| rs752178220 | 3:113,376,918 | G/C | — | uncertain significance |
| rs1221112214 | 3:113,376,924 | A/G | — | uncertain significance |
| rs768077848 | 3:113,376,931 | C/G | — | uncertain significance |
| rs754872745 | 3:113,376,960 | T/C | — | uncertain significance |
| rs1947402260 | 3:113,376,977 | A/T | — | uncertain significance |
| rs777733845 | 3:113,377,152 | A/G | — | uncertain significance |
| rs369926410 | 3:113,377,185 | T/C | — | likely benign |
| rs112398601 | 3:113,377,207 | T/C | — | uncertain significance |
| rs992623643 | 3:113,377,213 | C/G | — | uncertain significance |
| rs369163471 | 3:113,377,242 | C/T | — | uncertain significance |
| rs199925733 | 3:113,377,261 | T/C | — | uncertain significance |
| rs781132726 | 3:113,377,267 | T/C | — | uncertain significance |
| rs369937735 | 3:113,377,277 | G/A | — | likely benign |
| rs867278379 | 3:113,377,279 | C/T | — | uncertain significance |
| rs202216244 | 3:113,377,290 | T/C | — | uncertain significance |
| rs201503417 | 3:113,377,321 | C/T | — | uncertain significance |
| rs771302849 | 3:113,377,411 | C/A | — | conflicting classifications of pathogenicity |
| rs780497223 | 3:113,377,552 | T/C | — | uncertain significance |
| rs372311890 | 3:113,377,558 | C/G | — | uncertain significance |
| rs200212545 | 3:113,377,657 | C/A | — | uncertain significance |
| rs200386925 | 3:113,377,819 | T/C | — | likely benign |
| rs370570519 | 3:113,377,867 | T/C | — | likely benign |
| rs760900951 | 3:113,377,887 | G/A | — | uncertain significance |
| rs1264928983 | 3:113,377,909 | A/T | — | uncertain significance |
| rs1427893883 | 3:113,378,152 | T/C | — | uncertain significance |
| rs755745381 | 3:113,378,193 | G/T | — | uncertain significance |
| rs1211746985 | 3:113,378,235 | C/T | — | likely benign |
| rs2549656830 | 3:113,378,319 | G/A | — | uncertain significance |
| rs776056433 | 3:113,378,481 | G/A | — | uncertain significance |
| rs374317802 | 3:113,378,590 | T/G | — | uncertain significance |
| rs183889251 | 3:113,378,610 | G/A | — | uncertain significance |
| rs199640873 | 3:113,378,722 | G/C | — | uncertain significance |
| rs1423784002 | 3:113,378,814 | G/T | — | uncertain significance |
| rs541906719 | 3:113,379,097 | T/C | — | uncertain significance |
| rs777541217 | 3:113,379,124 | T/C | — | uncertain significance |
| rs1246760273 | 3:113,379,272 | G/C | — | uncertain significance |
| rs1559711104 | 3:113,379,327 | G/A | — | uncertain significance |
| rs373054683 | 3:113,379,357 | C/T | — | uncertain significance |
| rs2549658316 | 3:113,379,391 | C/T | — | uncertain significance |
| rs201864951 | 3:113,379,544 | C/T | — | likely benign |
| rs771615561 | 3:113,379,603 | G/A | — | uncertain significance |
| rs367902928 | 3:113,379,699 | T/C | — | uncertain significance |
| rs2549658808 | 3:113,379,742 | A/G | — | likely benign |
| rs1947472922 | 3:113,379,757 | C/A | — | uncertain significance |
| rs748718324 | 3:113,379,772 | T/C | — | uncertain significance |
Showing 100 of 109 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.