MAMDC4

MAM domain containing 4

Summary

Predicted to enable protein histidine phosphatase activity. Predicted to be involved in peptidyl-histidine dephosphorylation. Predicted to be located in cytosol. [provided by Alliance of Genome Resources, Apr 2025]

Known Variants141 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs771723588	9:139,747,565	G/C	—	uncertain significance
rs147821303	9:139,747,571	G/T	—	uncertain significance
rs764284938	9:139,747,572	C/G	—	uncertain significance
rs146504383	9:139,747,610	G/A	—	uncertain significance
rs2491104764	9:139,747,776	C/T	—	uncertain significance
rs149340579	9:139,747,787	G/A	—	uncertain significance
rs763614993	9:139,747,802	G/A	—	uncertain significance
rs761467290	9:139,747,884	C/T	—	uncertain significance
rs372480281	9:139,747,887	A/T	—	uncertain significance
rs576315462	9:139,748,020	C/G	—	uncertain significance
rs764894543	9:139,748,026	G/A	—	uncertain significance
rs1249404303	9:139,748,042	C/T	—	uncertain significance
rs776224564	9:139,748,069	G/A	—	uncertain significance
rs377182052	9:139,748,081	C/T	—	uncertain significance
rs769945042	9:139,748,243	C/T	—	uncertain significance
rs148622184	9:139,748,300	T/C	—	uncertain significance
rs553852620	9:139,748,339	C/T	—	uncertain significance
rs147857293	9:139,748,457	C/T	—	uncertain significance
rs2491106394	9:139,748,469	C/T	—	uncertain significance
rs763702002	9:139,748,480	G/A	—	uncertain significance
rs2491106821	9:139,748,663	C/T	—	uncertain significance
rs565967283	9:139,748,666	C/T	—	uncertain significance
rs2491106865	9:139,748,680	C/T	—	uncertain significance
rs552115419	9:139,748,719	G/A	—	uncertain significance
rs772823251	9:139,748,740	G/A	—	uncertain significance
rs117376465	9:139,748,748	C/T	—	likely benign
rs756007411	9:139,748,755	G/A	—	uncertain significance
rs775367570	9:139,748,759	A/G	—	uncertain significance
rs373644042	9:139,749,018	C/T	—	uncertain significance
rs142114032	9:139,749,068	G/C	—	uncertain significance
rs144788206	9:139,749,083	C/T	—	uncertain significance
rs894934854	9:139,749,098	C/A	—	uncertain significance
rs956680752	9:139,749,108	A/G	—	uncertain significance
rs147996833	9:139,749,114	G/A	—	likely benign
rs141677206	9:139,749,229	C/T	missense variant	—
rs780178024	9:139,749,232	T/C	—	uncertain significance
rs370273159	9:139,749,237	G/A	—	uncertain significance
rs144236396	9:139,749,270	G/A	—	uncertain significance
rs777901953	9:139,749,417	C/G	—	uncertain significance
rs61736295	9:139,749,464	G/A	—	uncertain significance
rs766243011	9:139,749,467	C/A	—	uncertain significance
rs201981906	9:139,749,494	C/T	—	uncertain significance
rs754377726	9:139,749,530	C/T	—	uncertain significance
rs1357590465	9:139,749,538	C/T	—	likely benign
rs1163282918	9:139,749,716	C/A	—	uncertain significance
rs370858940	9:139,749,718	G/A	—	uncertain significance
rs751127916	9:139,749,739	G/A	—	uncertain significance
rs780756945	9:139,749,742	G/A	—	uncertain significance
rs768546916	9:139,749,753	C/A	—	uncertain significance
rs371469925	9:139,749,754	G/A	—	uncertain significance
rs145077934	9:139,749,788	C/T	—	likely benign
rs760042018	9:139,749,933	C/A	—	uncertain significance
rs759313529	9:139,749,942	C/A	—	uncertain significance
rs765112853	9:139,749,943	C/T	—	uncertain significance
rs200879576	9:139,749,955	G/A	—	uncertain significance
rs368988631	9:139,749,969	T/A	—	uncertain significance
rs764918248	9:139,749,978	G/A	—	uncertain significance
rs762788461	9:139,749,982	A/G	—	uncertain significance
rs979623606	9:139,750,005	G/C	—	uncertain significance
rs199522336	9:139,750,041	T/C	—	uncertain significance
rs1404362104	9:139,750,051	G/A	—	uncertain significance
rs761650131	9:139,750,053	G/A	—	uncertain significance
rs2491111196	9:139,750,205	C/G	—	uncertain significance
rs1424754873	9:139,750,234	G/A	—	uncertain significance
rs368190960	9:139,750,240	C/T	—	uncertain significance
rs770790837	9:139,750,248	G/C	—	uncertain significance
rs544641095	9:139,750,249	T/C	—	uncertain significance
rs2491111391	9:139,750,271	A/G	—	uncertain significance
rs199571455	9:139,750,287	T/A	—	uncertain significance
rs1405217576	9:139,750,298	C/T	—	uncertain significance
rs1429716154	9:139,750,490	C/T	—	uncertain significance
rs138991199	9:139,750,500	G/C	—	uncertain significance
rs200042465	9:139,750,520	C/G	—	uncertain significance
rs994414709	9:139,750,584	T/C	—	uncertain significance
rs374261157	9:139,751,182	C/T	—	uncertain significance
rs113743118	9:139,751,224	C/T	—	uncertain significance
rs1210443865	9:139,751,231	G/A	—	likely benign
rs1180364314	9:139,751,245	C/T	—	uncertain significance
rs370030169	9:139,751,246	G/A	—	likely benign
rs1849014118	9:139,751,383	C/G	—	uncertain significance
rs773975470	9:139,751,448	A/C	—	uncertain significance
rs143519494	9:139,751,625	C/T	—	uncertain significance
rs368530422	9:139,751,626	G/A	—	uncertain significance
rs760754061	9:139,751,668	C/T	—	uncertain significance
rs754033917	9:139,751,671	G/A	—	uncertain significance
rs748397900	9:139,751,691	C/T	—	uncertain significance
rs774237103	9:139,751,838	G/A	—	uncertain significance
rs369775481	9:139,751,843	G/A	—	uncertain significance
rs1215797512	9:139,751,846	T/C	—	uncertain significance
rs200778498	9:139,751,879	G/A	—	uncertain significance
rs1849022567	9:139,751,895	G/A	—	uncertain significance
rs776665084	9:139,751,943	C/G	—	uncertain significance
rs747017555	9:139,751,957	G/A	—	uncertain significance
rs1416811189	9:139,751,991	A/G	—	uncertain significance
rs143805848	9:139,752,132	C/G	—	uncertain significance
rs771326340	9:139,752,143	G/A	—	uncertain significance
rs773909667	9:139,752,153	G/A	—	uncertain significance
rs767464516	9:139,752,162	C/T	—	uncertain significance
rs1345980569	9:139,752,431	G/A	—	uncertain significance
rs557204357	9:139,752,440	G/A	—	likely benign

Showing 100 of 141 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.