MAGEC1

MAGE family member C1

Summary

This gene is a member of the melanoma antigen gene (MAGE) family. The proteins of this family are tumor-specific antigens that can be recognized by autologous cytolytic T lymphocytes. This protein contains a large number of unique short repetitive sequences in front of the MAGE-homologous sequence, and therefore is about 800 aa longer than the other MAGE proteins. [provided by RefSeq, Jul 2008]

Known Variants106 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs113574601	X:140,992,860	T/C	—	likely benign
rs778031734	X:140,993,308	A/T	—	uncertain significance
rs377530412	X:140,993,351	C/T	—	uncertain significance
rs571922643	X:140,993,360	G/T	—	uncertain significance
rs2521758049	X:140,993,393	A/G	—	uncertain significance
rs141277731	X:140,993,468	A/G	—	uncertain significance
rs780656248	X:140,993,473	C/A	—	uncertain significance
rs2018180078	X:140,993,588	G/A	—	uncertain significance
rs374380387	X:140,993,600	C/G	—	likely benign
rs752350196	X:140,993,617	A/C	—	uncertain significance
rs770420459	X:140,993,737	C/T	—	uncertain significance
rs530144762	X:140,993,759	T/C	—	uncertain significance
rs763589156	X:140,993,800	C/T	—	uncertain significance
rs140674361	X:140,993,807	T/C	—	conflicting classifications of pathogenicity
rs766166929	X:140,993,814	C/T	—	likely benign
rs138331708	X:140,993,819	T/C	—	uncertain significance
rs202080559	X:140,993,842	C/T	—	likely benign
rs176039	X:140,993,877	C/A	—	likely benign
rs1397011686	X:140,993,879	A/G	—	uncertain significance
rs150761200	X:140,993,884	C/G	—	uncertain significance
rs146512531	X:140,993,899	G/A	—	uncertain significance
rs176040	X:140,993,905	C/G	—	benign
rs140572967	X:140,993,908	T/G	—	benign
rs76335605	X:140,993,926	C/T	—	likely benign
rs139312704	X:140,993,957	C/G	—	likely benign
rs145720656	X:140,993,964	T/A	—	likely benign
rs112112998	X:140,994,005	T/G	—	uncertain significance
rs143600642	X:140,994,008	G/C	—	likely benign
rs879185216	X:140,994,109	G/A	—	likely benign
rs879070866	X:140,994,113	G/C	—	conflicting classifications of pathogenicity
rs372423529	X:140,994,140	G/A	—	uncertain significance
rs59520182	X:140,994,190	C/G	—	conflicting classifications of pathogenicity
rs57528288	X:140,994,214	A/G	—	likely benign
rs764351838	X:140,994,218	C/G	—	likely benign
rs57859161	X:140,994,220	T/A	—	uncertain significance
rs767901098	X:140,994,221	C/G	—	uncertain significance
rs57133902	X:140,994,234	T/C	—	likely benign
rs758270463	X:140,994,242	T/C	—	uncertain significance
rs141749909	X:140,994,247	A/C	—	likely benign
rs145693793	X:140,994,252	C/A	—	conflicting classifications of pathogenicity
rs58302943	X:140,994,261	T/C	—	likely benign
rs59612804	X:140,994,270	T/A	—	likely benign
rs762022183	X:140,994,271	G/A	—	likely benign
rs148009378	X:140,994,295	C/G	—	likely benign
rs760984005	X:140,994,326	C/G	—	conflicting classifications of pathogenicity
rs376320957	X:140,994,329	C/G	—	uncertain significance
rs56755295	X:140,994,332	T/C	—	likely benign
rs144210857	X:140,994,365	C/T	—	conflicting classifications of pathogenicity
rs148715421	X:140,994,367	C/T	—	conflicting classifications of pathogenicity
rs201069092	X:140,994,376	A/G	—	uncertain significance
rs147478169	X:140,994,386	C/A	—	uncertain significance
rs140096964	X:140,994,389	T/C	—	uncertain significance
rs960149626	X:140,994,391	G/A	—	uncertain significance
rs1180569039	X:140,994,392	A/G	—	uncertain significance
rs762439291	X:140,994,400	C/G	—	uncertain significance
rs60282368	X:140,994,410	C/T	—	likely benign
rs200293020	X:140,994,424	A/G	—	likely benign
rs201520870	X:140,994,428	C/T	—	uncertain significance
rs757647823	X:140,994,437	T/C	—	uncertain significance
rs764103583	X:140,994,505	C/G	—	uncertain significance
rs59536220	X:140,994,540	T/C	—	likely benign
rs61701368	X:140,994,556	T/G	—	uncertain significance
rs138737656	X:140,994,562	C/G	—	uncertain significance
rs1259978596	X:140,994,565	T/C	—	uncertain significance
rs2521766726	X:140,994,571	A/G	—	uncertain significance
rs144000269	X:140,994,610	C/T	—	uncertain significance
rs780956948	X:140,994,650	C/T	—	uncertain significance
rs776926725	X:140,994,692	G/A	—	uncertain significance
rs1266317776	X:140,994,775	C/T	—	uncertain significance
rs754835611	X:140,994,826	C/T	—	uncertain significance
rs2124150109	X:140,994,829	T/C	—	uncertain significance
rs766075324	X:140,994,900	G/T	—	uncertain significance
rs769866187	X:140,994,965	C/T	—	uncertain significance
rs2521771090	X:140,995,398	C/G	—	uncertain significance
rs139916073	X:140,995,430	G/T	—	uncertain significance
rs748296864	X:140,995,522	C/T	—	uncertain significance
rs1477243513	X:140,995,547	C/T	—	uncertain significance
rs1430540529	X:140,995,556	G/A	—	uncertain significance
rs370950783	X:140,995,639	T/C	—	uncertain significance
rs41299076	X:140,995,712	G/T	missense variant	—
rs772220933	X:140,995,783	A/T	—	uncertain significance
rs760931235	X:140,995,804	A/G	—	uncertain significance
rs769947583	X:140,995,845	G/T	—	conflicting classifications of pathogenicity
rs140839403	X:140,995,867	G/A	—	uncertain significance
rs1569478110	X:140,995,894	C/G	—	uncertain significance
rs149706249	X:140,995,904	C/T	—	uncertain significance
rs141478517	X:140,995,940	G/C	—	uncertain significance
rs1170848045	X:140,996,015	A/G	—	uncertain significance
rs376091237	X:140,996,071	T/C	—	uncertain significance
rs752610012	X:140,996,090	A/G	—	uncertain significance
rs778042504	X:140,996,242	G/T	—	uncertain significance
rs1927029525	X:140,996,296	G/A	—	uncertain significance
rs755152921	X:140,996,320	C/G	—	uncertain significance
rs113554474	X:140,996,339	A/C	—	likely benign
rs769272586	X:140,996,350	C/G	—	uncertain significance
rs148626954	X:140,996,360	G/A	—	uncertain significance
rs761623332	X:140,996,362	G/C	—	uncertain significance
rs1320290676	X:140,996,372	A/G	—	uncertain significance
rs375062567	X:140,996,373	C/A	—	uncertain significance
rs200237572	X:140,996,387	G/A	—	uncertain significance

Showing 100 of 106 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.