CMIP

c-Maf inducing protein

Summary

This gene encodes a c-Maf inducing protein that plays a role in T-cell signaling pathway. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2011]

Known Variants101 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs757093645	16:81,478,865	T/G	—	uncertain significance
rs951764656	16:81,478,878	G/A	—	uncertain significance
rs2507848196	16:81,478,886	C/G	—	uncertain significance
rs763186205	16:81,478,926	T/C	—	uncertain significance
rs1373813031	16:81,478,936	C/G	—	likely benign
rs1905769827	16:81,479,055	C/G	—	uncertain significance
rs2507849119	16:81,479,120	G/A	—	uncertain significance
rs1332740299	16:81,479,142	C/T	—	uncertain significance
rs16955379	16:81,489,373	C/T	intron variant	—
rs9746731	16:81,492,643	A/T	—	—
rs12928482	16:81,513,871	G/C	—	—
rs9928008	16:81,517,598	G/A	regulatory region variant	—
rs74812392	16:81,519,378	A/G	regulatory region variant	—
rs56793457	16:81,521,705	C/G	—	—
rs57795729	16:81,521,708	C/A	—	—
rs17197883	16:81,523,013	T/C	intron variant	—
rs881005	16:81,526,977	G/A	regulatory region variant	—
rs116711199	16:81,531,515	T/C	regulatory region variant	—
rs11641142	16:81,533,922	C/G	intron variant	—
rs2925979	16:81,534,790	T/A	—	—
rs55683214	16:81,536,191	G/C	—	—
rs77384835	16:81,551,168	T/G	regulatory region variant	—
rs2966104	16:81,557,195	T/A	—	—
rs7201098	16:81,559,216	G/A	intron variant	—
rs7201103	16:81,559,220	G/C	intron variant	—
rs12933858	16:81,566,121	C/A	—	—
rs77531223	16:81,566,518	C/A	regulatory region variant	—
rs11644696	16:81,572,093	G/C	—	—
rs13333615	16:81,578,104	C/G	—	—
rs76294479	16:81,581,584	C/T	intron variant	—
rs35610022	16:81,586,901	C/T	regulatory region variant	—
rs76006132	16:81,588,571	G/T	intron variant	—
rs2911280	16:81,591,313	A/G	intron variant	—
rs538162868	16:81,595,438	A/C	—	—
rs12931242	16:81,604,778	T/G	intron variant	—
rs7196195	16:81,609,598	T/A	—	—
rs12930698	16:81,610,598	A/C	—	—
rs12934751	16:81,610,667	T/C	intron variant	—
rs57603843	16:81,641,207	C/T	—	likely benign
rs1326286805	16:81,641,208	G/A	—	uncertain significance
rs772246525	16:81,641,220	G/A	—	uncertain significance
rs114894868	16:81,641,226	C/T	—	benign
rs528248123	16:81,654,492	C/T	—	likely benign
rs774161722	16:81,685,859	G/T	—	uncertain significance
rs1597199609	16:81,685,883	C/T	—	likely benign
rs770230656	16:81,685,925	A/G	—	uncertain significance
rs2508942380	16:81,691,409	A/T	—	uncertain significance
rs376121640	16:81,694,492	A/G	—	uncertain significance
rs552521007	16:81,694,500	T/G	—	likely benign
rs1597214739	16:81,697,864	C/T	—	likely benign
rs1464550853	16:81,697,888	G/A	—	likely benign
rs371335167	16:81,697,894	G/A	—	likely benign
rs1597214856	16:81,697,964	C/T	—	likely benign
rs754812064	16:81,703,767	A/C	—	likely benign
rs757849921	16:81,703,787	A/G	—	uncertain significance
rs201681184	16:81,703,806	C/T	—	benign
rs183075361	16:81,703,860	C/T	—	benign
rs376811403	16:81,705,607	G/T	—	likely benign
rs544242568	16:81,705,652	C/G	—	likely benign
rs6564907	16:81,705,971	T/C	intron variant	—
rs1904474095	16:81,711,879	G/A	—	uncertain significance
rs375947777	16:81,711,931	G/A	—	likely benign
rs776492922	16:81,711,950	T/C	—	likely benign
rs368498490	16:81,712,002	C/T	—	uncertain significance
rs370956514	16:81,712,025	T/G	—	uncertain significance
rs375506984	16:81,712,033	C/T	—	likely benign
rs35429777	16:81,712,087	G/A	—	benign
rs202217278	16:81,712,095	C/T	—	uncertain significance
rs1478649391	16:81,712,155	C/T	—	uncertain significance
rs1228524163	16:81,712,185	C/A	—	uncertain significance
rs369769411	16:81,712,200	C/G	—	uncertain significance
rs554256376	16:81,712,205	G/A	—	uncertain significance
rs34119643	16:81,712,213	C/T	—	benign
rs371495274	16:81,712,243	C/A	—	benign
rs55669104	16:81,723,098	T/A	—	—
rs201626483	16:81,725,376	C/G	—	benign
rs1597258512	16:81,726,786	C/G	—	uncertain significance
rs1047480684	16:81,727,068	G/T	—	uncertain significance
rs199973612	16:81,727,075	G/A	—	uncertain significance
rs60152409	16:81,730,185	C/T	—	benign
rs374999407	16:81,730,195	G/A	—	uncertain significance
rs1296944404	16:81,730,228	G/A	—	uncertain significance
rs372884363	16:81,730,242	C/T	—	likely benign
rs545129438	16:81,730,248	T/C	—	likely benign
rs1386252046	16:81,730,264	G/A	—	uncertain significance
rs79979027	16:81,730,276	C/A	—	benign
rs371157898	16:81,730,277	G/A	—	likely benign
rs768759672	16:81,730,282	G/A	—	likely benign
rs183876152	16:81,733,292	G/A	—	benign
rs527523022	16:81,733,328	A/G	—	likely benign
rs369298377	16:81,735,322	A/G	—	uncertain significance
rs377104079	16:81,735,359	G/A	—	uncertain significance
rs375897973	16:81,735,413	C/T	—	likely benign
rs377241916	16:81,737,642	C/T	—	likely benign
rs2509250847	16:81,737,653	T/G	—	uncertain significance
rs560316334	16:81,737,694	C/T	—	likely benign
rs72831128	16:81,737,695	A/G	—	benign
rs201316817	16:81,739,118	C/A	—	benign
rs554858194	16:81,739,145	C/G	—	likely benign
rs368824151	16:81,740,650	C/T	—	likely benign

Showing 100 of 101 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.