PRRC2C

proline rich coiled-coil 2C

Summary

Enables RNA binding activity. Involved in stress granule assembly. Located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants125 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs181559114	1:171,459,913	A/G	upstream gene variant	—
rs143515117	1:171,481,304	A/T	—	uncertain significance
rs532232804	1:171,481,575	A/G	—	—
rs371016782	1:171,482,236	A/G	—	uncertain significance
rs376424403	1:171,484,960	A/G	—	uncertain significance
rs541228951	1:171,486,942	A/G	—	uncertain significance
rs1673948252	1:171,492,393	G/C	—	uncertain significance
rs1673956861	1:171,492,434	A/T	—	uncertain significance
rs777304328	1:171,492,461	A/G	—	uncertain significance
rs36013361	1:171,492,641	C/G	—	uncertain significance
rs573339337	1:171,493,971	G/A	—	uncertain significance
rs374100810	1:171,494,043	A/G	—	uncertain significance
rs767973539	1:171,494,069	A/G	—	uncertain significance
rs372459385	1:171,496,966	A/G	—	uncertain significance
rs1386678705	1:171,501,509	C/T	—	uncertain significance
rs2527316161	1:171,501,518	C/A	—	uncertain significance
rs1261444981	1:171,501,612	A/G	—	uncertain significance
rs773403036	1:171,501,663	G/C	—	uncertain significance
rs200015770	1:171,501,679	G/A	—	likely benign
rs1222081434	1:171,501,771	G/A	—	uncertain significance
rs139995932	1:171,501,777	G/A	—	uncertain significance
rs147935820	1:171,501,788	C/T	—	uncertain significance
rs373214431	1:171,501,938	C/T	—	uncertain significance
rs765104696	1:171,501,990	A/G	—	uncertain significance
rs1474992002	1:171,502,068	A/G	—	uncertain significance
rs147808088	1:171,504,629	G/C	—	uncertain significance
rs1229455482	1:171,505,193	A/G	—	uncertain significance
rs138658625	1:171,505,241	C/A	—	likely benign
rs376665075	1:171,505,291	A/G	—	uncertain significance
rs1223429583	1:171,506,503	G/A	—	uncertain significance
rs753648367	1:171,509,202	G/C	—	uncertain significance
rs372892362	1:171,509,211	G/A	—	uncertain significance
rs75723046	1:171,509,275	T/C	—	likely benign
rs1295462277	1:171,509,277	C/T	—	uncertain significance
rs772889986	1:171,509,289	C/T	—	uncertain significance
rs370158523	1:171,509,343	G/A	—	uncertain significance
rs758574187	1:171,509,372	C/T	—	uncertain significance
rs201752804	1:171,509,373	G/A	—	uncertain significance
rs147534952	1:171,509,454	A/G	—	uncertain significance
rs2527459442	1:171,509,455	A/C	—	uncertain significance
rs770555436	1:171,509,465	A/G	—	uncertain significance
rs200371697	1:171,509,490	T/C	—	likely benign
rs758929942	1:171,509,585	C/T	—	uncertain significance
rs2527464342	1:171,509,714	G/A	—	uncertain significance
rs2527465462	1:171,509,742	A/G	—	uncertain significance
rs748920176	1:171,509,750	G/T	—	uncertain significance
rs143283766	1:171,509,769	C/T	—	uncertain significance
rs867099365	1:171,509,789	C/T	—	uncertain significance
rs764588047	1:171,509,820	C/T	—	uncertain significance
rs754488391	1:171,509,874	C/T	—	uncertain significance
rs747853338	1:171,509,892	C/G	—	uncertain significance
rs777309495	1:171,510,005	G/A	—	uncertain significance
rs1209621899	1:171,510,062	C/G	—	uncertain significance
rs767926177	1:171,510,066	G/A	—	uncertain significance
rs1361433514	1:171,510,110	C/T	—	uncertain significance
rs780171057	1:171,510,125	A/G	—	uncertain significance
rs774617437	1:171,510,159	A/C	—	uncertain significance
rs750203323	1:171,510,240	G/T	—	uncertain significance
rs61814671	1:171,510,307	C/T	—	likely benign
rs372374862	1:171,510,344	C/T	—	uncertain significance
rs530214687	1:171,510,345	G/A	—	uncertain significance
rs778929653	1:171,510,362	T/C	—	uncertain significance
rs898192403	1:171,510,473	A/G	—	uncertain significance
rs373909749	1:171,510,497	A/G	—	uncertain significance
rs186657370	1:171,510,519	C/G	—	uncertain significance
rs1399560082	1:171,510,540	A/G	—	uncertain significance
rs2527485141	1:171,510,621	G/A	—	uncertain significance
rs142373462	1:171,510,660	G/A	—	uncertain significance
rs143393069	1:171,510,692	C/T	—	uncertain significance
rs146224112	1:171,510,723	G/A	—	uncertain significance
rs74122867	1:171,510,733	G/T	—	uncertain significance
rs142821409	1:171,510,753	A/T	—	uncertain significance
rs773293361	1:171,510,780	C/T	—	uncertain significance
rs570949281	1:171,510,809	A/G	—	uncertain significance
rs147829253	1:171,510,868	G/C	—	uncertain significance
rs2527492986	1:171,510,896	C/G	—	uncertain significance
rs142318394	1:171,511,025	C/G	—	likely benign
rs202088651	1:171,511,139	G/C	—	uncertain significance
rs781265114	1:171,511,218	G/C	—	uncertain significance
rs1231239805	1:171,511,262	C/T	—	uncertain significance
rs141606555	1:171,511,272	G/A	—	uncertain significance
rs1340215354	1:171,514,755	C/G	—	uncertain significance
rs773951826	1:171,514,775	C/A	—	uncertain significance
rs35039375	1:171,516,863	A/G	intron variant	—
rs563519350	1:171,525,905	T/C	—	—
rs2527029911	1:171,526,535	G/T	—	uncertain significance
rs574479091	1:171,526,553	A/G	—	uncertain significance
rs2527030924	1:171,526,565	C/T	—	uncertain significance
rs867352775	1:171,526,598	A/G	—	likely benign
rs553054787	1:171,527,040	C/T	—	uncertain significance
rs746127461	1:171,527,175	C/A	—	uncertain significance
rs377723398	1:171,527,189	A/G	—	uncertain significance
rs148813704	1:171,527,237	A/G	—	likely benign
rs772389306	1:171,530,172	C/T	—	uncertain significance
rs752839002	1:171,535,538	C/T	—	uncertain significance
rs952112250	1:171,535,843	G/A	—	uncertain significance
rs776298228	1:171,535,908	G/C	—	uncertain significance
rs188936019	1:171,536,685	C/T	intron variant	—
rs779003770	1:171,537,440	A/G	—	uncertain significance
rs2527310120	1:171,540,477	C/G	—	uncertain significance

Showing 100 of 125 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.