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.