CTRC

chymotrypsin C

Summary

This gene encodes a member of the peptidase S1 family. The encoded protein is a serum calcium-decreasing factor that has chymotrypsin-like protease activity. Alternatively spliced transcript variants have been observed, but their full-length nature has not been determined. [provided by RefSeq, Jul 2008]

Known Variants474 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs183658182	1:15,764,902	C/T	—	conflicting classifications of pathogenicity
rs1708075349	1:15,764,959	C/T	—	uncertain significance
rs1195152458	1:15,764,960	C/T	—	uncertain significance
rs544668774	1:15,764,961	A/G	—	conflicting classifications of pathogenicity
rs1455019932	1:15,764,962	T/C	—	likely pathogenic
rs2526285179	1:15,764,965	T/G	—	uncertain significance
rs774324080	1:15,764,966	G/A	—	likely benign
rs1343524121	1:15,764,967	G/T	—	uncertain significance
rs2526285185	1:15,764,968	G/A	—	uncertain significance
rs761548318	1:15,764,971	T/C	—	uncertain significance
rs1455830684	1:15,764,972	C/T	—	likely benign
rs933703	1:15,764,973	A/T	—	uncertain significance
rs1060504817	1:15,764,975	T/C	—	likely benign
rs1424073260	1:15,764,976	G/A	—	uncertain significance
rs1279354220	1:15,764,981	C/T	—	likely benign
rs767349844	1:15,764,982	G/A	—	uncertain significance
rs2526285336	1:15,764,983	C/G	—	uncertain significance
rs749888586	1:15,764,985	G/T	—	uncertain significance
rs772818172	1:15,764,986	C/T	—	uncertain significance
rs374821228	1:15,764,987	G/A	—	conflicting classifications of pathogenicity
rs758984378	1:15,764,989	T/C	—	uncertain significance
rs2526285371	1:15,764,990	C/G	—	likely benign
rs1708076225	1:15,764,991	T/C	—	likely benign
rs2526285382	1:15,764,993	G/C	—	uncertain significance
rs1318452999	1:15,764,995	C/T	—	uncertain significance
rs747431847	1:15,764,999	T/C	—	conflicting classifications of pathogenicity
rs1222161661	1:15,765,004	A/G	—	uncertain significance
rs890047179	1:15,765,006	C/T	—	uncertain significance
rs369827801	1:15,765,007	G/A	—	likely benign
rs564455614	1:15,765,010	G/A	—	likely benign
rs781396039	1:15,765,012	G/C	—	likely benign
rs1457043033	1:15,765,014	T/C	—	likely benign
rs1708076823	1:15,765,018	G/A	—	likely benign
rs142888713	1:15,765,024	G/A	—	likely benign
rs2272909	1:15,765,175	C/A	—	benign
rs117858254	1:15,766,618	A/T	—	benign
rs1252698635	1:15,766,785	T/C	—	likely benign
rs372788092	1:15,766,790	C/T	—	likely benign
rs781284605	1:15,766,791	C/A	—	conflicting classifications of pathogenicity
rs765777463	1:15,766,801	A/G	—	conflicting classifications of pathogenicity
rs2526289306	1:15,766,802	G/T	—	uncertain significance
rs753438186	1:15,766,803	C/G	—	uncertain significance
rs200576965	1:15,766,807	G/A	—	uncertain significance
rs1168683208	1:15,766,809	G/A	—	likely benign
rs751854409	1:15,766,810	G/T	—	uncertain significance
rs2103289251	1:15,766,811	T/C	—	uncertain significance
rs757630885	1:15,766,813	C/T	—	uncertain significance
rs2526289389	1:15,766,818	C/T	—	likely benign
rs2526289392	1:15,766,819	T/C	—	uncertain significance
rs781341140	1:15,766,821	C/T	—	likely benign
rs533967597	1:15,766,823	C/T	—	conflicting classifications of pathogenicity
rs756394210	1:15,766,824	G/A	—	likely benign
rs1241494944	1:15,766,826	C/T	—	uncertain significance
rs2526289428	1:15,766,827	C/T	—	likely benign
rs1212285395	1:15,766,828	A/G	—	uncertain significance
rs2526289455	1:15,766,831	C/T	—	likely benign
rs2526289459	1:15,766,832	T/C	—	uncertain significance
rs1708111860	1:15,766,833	A/G	—	likely benign
rs749455108	1:15,766,836	C/T	—	conflicting classifications of pathogenicity
rs768414501	1:15,766,837	G/A	—	conflicting classifications of pathogenicity
rs910253285	1:15,766,838	C/T	—	uncertain significance
rs779009847	1:15,766,839	C/T	—	likely benign
rs747905422	1:15,766,840	C/T	—	pathogenic
rs772024986	1:15,766,841	G/T	—	uncertain significance
rs2526289507	1:15,766,844	T/C	—	uncertain significance
rs1258820133	1:15,766,846	G/A	—	uncertain significance
rs2526289538	1:15,766,850	G/A	—	uncertain significance
rs184977421	1:15,766,858	G/A	—	likely benign
rs1421655402	1:15,766,861	G/T	—	uncertain significance
rs2526289576	1:15,766,863	C/T	—	likely benign
rs770675516	1:15,766,864	C/T	—	uncertain significance
rs145868278	1:15,766,865	G/A	—	likely benign
rs2526289603	1:15,766,866	G/A	—	likely benign
rs2526289616	1:15,766,869	C/T	—	likely benign
rs2526289630	1:15,766,873	A/C	—	uncertain significance
rs1708113042	1:15,766,875	C/A	—	uncertain significance
rs2526289677	1:15,766,882	T/C	—	uncertain significance
rs2526289681	1:15,766,884	G/A	—	likely pathogenic
rs901779500	1:15,766,887	G/A	—	conflicting classifications of pathogenicity
rs370612719	1:15,766,902	G/A	—	likely benign
rs762121956	1:15,766,903	G/C	—	likely benign
rs1300766611	1:15,766,907	G/A	—	likely benign
rs777418401	1:15,766,970	C/G	—	likely benign
rs1372740891	1:15,766,974	C/T	—	likely benign
rs1557508272	1:15,766,988	G/T	—	likely pathogenic
rs2526289973	1:15,766,989	A/T	—	uncertain significance
rs758920912	1:15,766,990	T/A	—	uncertain significance
rs1451404148	1:15,766,993	C/T	—	uncertain significance
rs2526289999	1:15,766,994	C/T	—	likely benign
rs769324644	1:15,766,995	C/T	—	uncertain significance
rs536812916	1:15,766,999	A/G	—	uncertain significance
rs1410389781	1:15,767,000	G/A	—	likely benign
rs78247007	1:15,767,001	T/C	—	uncertain significance
rs576621137	1:15,767,003	C/T	—	likely benign
rs2526290032	1:15,767,006	C/T	—	likely benign
rs1002224359	1:15,767,007	A/G	—	uncertain significance
rs1199793577	1:15,767,010	A/G	—	conflicting classifications of pathogenicity
rs77373944	1:15,767,012	C/T	—	benign
rs761118020	1:15,767,013	G/C	—	uncertain significance
rs2526290061	1:15,767,015	C/G	—	uncertain significance

Showing 100 of 474 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.