MAT2A

methionine adenosyltransferase 2A

Summary

The protein encoded by this gene catalyzes the production of S-adenosylmethionine (AdoMet) from methionine and ATP. AdoMet is the key methyl donor in cellular processes. [provided by RefSeq, Jun 2011]

Known Variants189 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs1446668	2:85,764,960	G/T	regulatory region variant	—
rs60048404	2:85,765,855	C/T	—	likely benign
rs60749033	2:85,765,937	G/T	—	likely benign
rs6733827	2:85,766,279	G/A	—	likely benign
rs147348486	2:85,766,300	G/A	—	likely benign
rs1057524274	2:85,766,363	C/T	—	likely benign
rs780678816	2:85,766,376	C/G	—	likely benign
rs761278339	2:85,766,389	A/G	—	likely benign
rs772772892	2:85,766,393	C/T	—	likely benign
rs202218397	2:85,766,396	C/T	—	likely benign
rs375636333	2:85,766,404	C/T	—	likely benign
rs781289274	2:85,766,416	C/T	—	likely benign
rs1691387581	2:85,766,418	G/A	—	uncertain significance
rs756268499	2:85,766,421	A/C	—	uncertain significance
rs780241796	2:85,766,422	G/A	—	likely benign
rs768987572	2:85,766,426	A/C	—	uncertain significance
rs779310038	2:85,766,427	A/G	—	uncertain significance
rs1375245079	2:85,766,431	C/T	—	likely benign
rs909244613	2:85,766,435	C/T	—	uncertain significance
rs748650397	2:85,766,438	G/C	—	uncertain significance
rs771488542	2:85,766,440	G/C	—	conflicting classifications of pathogenicity
rs139547506	2:85,766,442	C/T	—	uncertain significance
rs760251833	2:85,766,447	A/G	—	uncertain significance
rs776303477	2:85,766,449	C/G	—	uncertain significance
rs1287645133	2:85,766,458	C/A	—	likely benign
rs759450196	2:85,766,461	A/G	—	likely benign
rs142991697	2:85,766,464	C/T	—	likely benign
rs1691389356	2:85,766,465	C/T	—	uncertain significance
rs752605763	2:85,766,476	A/C	—	likely benign
rs372604021	2:85,766,482	G/T	—	likely benign
rs1170686756	2:85,766,485	C/T	—	likely benign
rs2529625235	2:85,766,494	C/A	—	likely benign
rs1691390438	2:85,766,515	C/T	—	likely benign
rs372557886	2:85,766,518	A/C	—	likely benign
rs1192760838	2:85,766,520	G/A	—	likely benign
rs780304998	2:85,766,521	C/T	—	likely benign
rs2289972	2:85,766,545	C/T	—	benign
rs2028900	2:85,767,735	C/T	regulatory region variant	—
rs2028899	2:85,767,969	C/A	—	likely benign
rs1436881741	2:85,768,198	T/C	—	likely benign
rs1273216076	2:85,768,200	T/C	—	likely benign
rs115257622	2:85,768,222	A/G	—	likely benign
rs1691466545	2:85,768,225	C/T	—	likely benign
rs570063081	2:85,768,234	T/C	—	likely benign
rs1573307911	2:85,768,255	G/A	—	likely benign
rs141686174	2:85,768,272	A/G	—	uncertain significance
rs761673664	2:85,768,296	T/C	—	likely benign
rs58507836	2:85,768,330	A/G	—	benign
rs774075656	2:85,768,365	C/T	—	likely benign
rs772066412	2:85,768,382	T/C	—	likely benign
rs535386066	2:85,768,385	T/G	—	likely benign
rs2529629515	2:85,768,427	C/T	—	likely benign
rs1292360465	2:85,768,454	G/A	—	likely benign
rs370638648	2:85,768,457	T/C	—	likely benign
rs924043399	2:85,768,464	G/A	—	likely benign
rs1392356231	2:85,768,467	G/C	—	uncertain significance
rs1573308038	2:85,768,484	T/C	—	likely benign
rs2103916591	2:85,768,494	T/G	—	uncertain significance
rs1691471820	2:85,768,496	C/T	—	likely benign
rs2529629608	2:85,768,512	T/C	—	likely benign
rs750871330	2:85,768,514	A/C	—	likely benign
rs1281552047	2:85,768,517	T/C	—	likely benign
rs116670686	2:85,768,570	A/G	—	benign
rs72940559	2:85,768,677	T/C	—	likely benign
rs370732107	2:85,768,709	C/T	—	likely benign
rs992234117	2:85,768,741	G/T	—	likely benign
rs2529630577	2:85,768,768	A/C	—	uncertain significance
rs974451464	2:85,768,778	C/T	—	likely benign
rs2103917082	2:85,768,780	T/G	—	uncertain significance
rs72940560	2:85,768,781	G/T	—	likely benign
rs377763337	2:85,768,787	A/T	—	likely benign
rs746976689	2:85,768,799	A/G	—	likely benign
rs2529630638	2:85,768,806	C/A	—	uncertain significance
rs2529630680	2:85,768,837	G/A	—	uncertain significance
rs770828359	2:85,768,840	A/G	—	uncertain significance
rs781182320	2:85,768,847	A/C	—	uncertain significance
rs772500142	2:85,768,884	G/T	—	likely benign
rs773508806	2:85,768,888	G/A	—	uncertain significance
rs62620249	2:85,768,900	T/C	—	benign
rs114500620	2:85,768,933	G/A	—	likely benign
rs747379918	2:85,768,949	T/C	—	conflicting classifications of pathogenicity
rs1239325849	2:85,768,972	C/T	—	likely benign
rs143610695	2:85,768,984	T/C	—	likely benign
rs2529630927	2:85,768,986	A/G	—	uncertain significance
rs759964992	2:85,768,990	G/A	—	likely benign
rs1691484259	2:85,768,991	T/A	—	uncertain significance
rs1691484335	2:85,769,005	C/T	—	likely benign
rs764743973	2:85,769,006	A/G	—	uncertain significance
rs756597114	2:85,769,008	T/C	—	likely benign
rs1352353696	2:85,769,011	C/T	—	likely benign
rs1016317798	2:85,769,023	G/A	—	likely benign
rs763696263	2:85,769,026	A/C	—	likely benign
rs891334425	2:85,769,034	A/G	—	uncertain significance
rs2529631223	2:85,769,044	A/G	—	likely benign
rs75623534	2:85,769,047	A/G	—	likely benign
rs568801854	2:85,769,050	C/T	—	likely benign
rs767382347	2:85,769,057	G/A	—	uncertain significance
rs750391168	2:85,769,065	G/A	—	likely benign
rs1363300276	2:85,769,083	T/C	—	likely benign
rs748275992	2:85,769,085	C/G	—	uncertain significance

Showing 100 of 189 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.