MN1
MN1 proto-oncogene, transcriptional regulator
Summary
Meningioma 1 (MN1) contains two sets of CAG repeats. It is disrupted by a balanced translocation (4;22) in a meningioma, and its inactivation may contribute to meningioma 32 pathogenesis. [provided by RefSeq, Jul 2008]
Known Variants201 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs28501997 | 22:28,146,770 | A/G | — | benign |
| rs2123873148 | 22:28,146,913 | G/T | — | likely pathogenic |
| rs568489325 | 22:28,146,947 | C/T | — | likely benign |
| rs1601319501 | 22:28,146,963 | C/T | — | conflicting classifications of pathogenicity |
| rs912955289 | 22:28,146,968 | T/C | — | uncertain significance |
| rs759860030 | 22:28,146,974 | C/T | — | uncertain significance |
| rs147334255 | 22:28,146,983 | G/A | stop gained | pathogenic |
| rs375104212 | 22:28,146,993 | G/A | — | likely benign |
| rs751081286 | 22:28,147,001 | C/T | — | uncertain significance |
| rs373855008 | 22:28,147,017 | G/A | — | likely benign |
| rs1601319598 | 22:28,147,031 | G/A | — | pathogenic |
| rs1601319615 | 22:28,147,049 | G/A | — | pathogenic |
| rs5762354 | 22:28,186,287 | G/A | intron variant | — |
| rs5762356 | 22:28,186,370 | A/G | intron variant | — |
| rs5752638 | 22:28,188,203 | T/C | intron variant | — |
| rs1933302820 | 22:28,192,754 | C/A | — | conflicting classifications of pathogenicity |
| rs761317200 | 22:28,192,787 | C/A | — | likely pathogenic |
| rs1297805962 | 22:28,192,788 | C/T | — | pathogenic |
| rs1246225634 | 22:28,192,793 | G/A | — | uncertain significance |
| rs1216829399 | 22:28,192,816 | G/C | — | uncertain significance |
| rs2517769852 | 22:28,192,849 | T/C | — | uncertain significance |
| rs2146315211 | 22:28,192,852 | C/T | — | likely pathogenic |
| rs2517769858 | 22:28,192,858 | G/A | — | uncertain significance |
| rs2517769871 | 22:28,192,867 | T/A | — | uncertain significance |
| rs2517769900 | 22:28,192,898 | T/G | — | uncertain significance |
| rs1490039052 | 22:28,192,975 | G/C | — | uncertain significance |
| rs1933308051 | 22:28,192,977 | G/T | — | pathogenic |
| rs45589739 | 22:28,192,982 | C/G | — | benign |
| rs748442678 | 22:28,192,988 | T/C | — | likely benign |
| rs772547139 | 22:28,192,998 | C/A | — | uncertain significance |
| rs751356858 | 22:28,193,075 | G/A | — | likely benign |
| rs45471598 | 22:28,193,097 | C/T | — | benign |
| rs745348338 | 22:28,193,106 | G/C | — | uncertain significance |
| rs545480570 | 22:28,193,133 | C/T | — | likely benign |
| rs935200470 | 22:28,193,149 | C/T | — | uncertain significance |
| rs776900381 | 22:28,193,161 | G/A | — | uncertain significance |
| rs778126684 | 22:28,193,175 | G/A | — | likely benign |
| rs2517770261 | 22:28,193,200 | G/C | — | uncertain significance |
| rs745596738 | 22:28,193,227 | G/A | — | uncertain significance |
| rs1271436703 | 22:28,193,229 | G/A | — | likely benign |
| rs1229819213 | 22:28,193,232 | C/A | — | likely benign |
| rs560561226 | 22:28,193,237 | G/C | — | uncertain significance |
| rs1451254445 | 22:28,193,240 | C/T | — | uncertain significance |
| rs1167931662 | 22:28,193,249 | C/T | — | uncertain significance |
| rs771925230 | 22:28,193,258 | C/T | — | uncertain significance |
| rs2517770333 | 22:28,193,278 | G/A | — | uncertain significance |
| rs757688741 | 22:28,193,281 | A/C | — | uncertain significance |
| rs377232565 | 22:28,193,294 | C/G | — | conflicting classifications of pathogenicity |
| rs561366930 | 22:28,193,372 | C/T | — | uncertain significance |
| rs750757950 | 22:28,193,391 | G/T | — | uncertain significance |
| rs1210709233 | 22:28,193,419 | G/A | — | uncertain significance |
| rs2146315783 | 22:28,193,428 | T/A | — | uncertain significance |
| rs200003316 | 22:28,193,448 | C/T | — | likely benign |
| rs1464999399 | 22:28,193,455 | C/T | — | uncertain significance |
| rs2517770553 | 22:28,193,468 | G/A | — | uncertain significance |
| rs2517770573 | 22:28,193,484 | C/G | — | uncertain significance |
| rs2517770595 | 22:28,193,512 | G/A | — | uncertain significance |
| rs1933323211 | 22:28,193,546 | C/G | — | likely benign |
| rs1383826053 | 22:28,193,549 | G/T | — | uncertain significance |
| rs1933325700 | 22:28,193,650 | T/C | — | uncertain significance |
| rs200253358 | 22:28,193,715 | G/A | — | likely benign |
| rs2146316004 | 22:28,193,719 | C/T | — | uncertain significance |
| rs1425710106 | 22:28,193,729 | C/T | — | uncertain significance |
| rs746306235 | 22:28,193,749 | G/A | — | uncertain significance |
| rs1933329089 | 22:28,193,780 | G/T | — | uncertain significance |
| rs2146316074 | 22:28,193,789 | C/G | — | uncertain significance |
| rs2517770933 | 22:28,193,795 | C/T | — | uncertain significance |
| rs201879268 | 22:28,193,807 | G/A | — | uncertain significance |
| rs1403168094 | 22:28,193,864 | G/C | — | uncertain significance |
| rs776690759 | 22:28,193,920 | G/A | — | uncertain significance |
| rs956458376 | 22:28,193,941 | T/C | — | uncertain significance |
| rs1458205467 | 22:28,193,942 | C/T | — | uncertain significance |
| rs1933333572 | 22:28,193,962 | T/C | — | uncertain significance |
| rs1568984319 | 22:28,193,992 | G/T | — | uncertain significance |
| rs758093453 | 22:28,194,004 | T/C | — | uncertain significance |
| rs1183955186 | 22:28,194,011 | C/A | — | uncertain significance |
| rs2517771236 | 22:28,194,058 | A/T | — | uncertain significance |
| rs2517771244 | 22:28,194,068 | G/A | — | pathogenic |
| rs1206845311 | 22:28,194,086 | T/C | — | uncertain significance |
| rs2517771346 | 22:28,194,163 | T/C | — | uncertain significance |
| rs776741937 | 22:28,194,187 | C/A | — | uncertain significance |
| rs1057018621 | 22:28,194,197 | C/T | — | uncertain significance |
| rs764493322 | 22:28,194,226 | G/A | — | uncertain significance |
| rs756889884 | 22:28,194,245 | C/T | — | uncertain significance |
| rs866112872 | 22:28,194,247 | C/T | — | uncertain significance |
| rs1043351855 | 22:28,194,254 | C/G | — | uncertain significance |
| rs1330671939 | 22:28,194,256 | C/T | — | uncertain significance |
| rs1255476603 | 22:28,194,269 | A/T | — | uncertain significance |
| rs749154826 | 22:28,194,276 | G/A | — | likely benign |
| rs1407090323 | 22:28,194,277 | C/A | — | uncertain significance |
| rs1933345344 | 22:28,194,293 | G/C | — | uncertain significance |
| rs1210433639 | 22:28,194,321 | C/T | — | uncertain significance |
| rs1007871535 | 22:28,194,357 | A/C | — | likely benign |
| rs1933348803 | 22:28,194,382 | G/A | — | uncertain significance |
| rs1247151797 | 22:28,194,386 | C/T | — | uncertain significance |
| rs1432467365 | 22:28,194,416 | G/T | — | uncertain significance |
| rs750109978 | 22:28,194,421 | C/A | — | uncertain significance |
| rs1367862555 | 22:28,194,424 | C/A | — | uncertain significance |
| rs565227821 | 22:28,194,474 | C/A | — | uncertain significance |
| rs758198222 | 22:28,194,478 | C/T | — | likely benign |
Showing 100 of 201 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.