RPS7

ribosomal protein S7

Summary

Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S7E family of ribosomal proteins. It is located in the cytoplasm. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]

Known Variants160 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs115090628	2:3,622,662	G/T	—	benign
rs142444366	2:3,622,850	C/T	—	likely benign
rs371620447	2:3,622,855	G/A	—	likely benign
rs186304514	2:3,622,873	C/T	—	uncertain significance
rs11558965	2:3,622,912	G/T	—	benign
rs563293592	2:3,622,915	C/T	—	uncertain significance
rs17552296	2:3,622,923	A/C	—	benign
rs573443780	2:3,622,932	C/T	—	uncertain significance
rs886055985	2:3,622,936	G/A	—	uncertain significance
rs2528176265	2:3,622,940	G/C	—	uncertain significance
rs1064796859	2:3,622,941	G/T	—	pathogenic
rs2528176273	2:3,622,942	T/A	—	pathogenic
rs530845583	2:3,622,953	C/T	—	likely benign
rs765604580	2:3,623,187	C/T	—	uncertain significance
rs751847851	2:3,623,197	G/A	—	uncertain significance
rs781456307	2:3,623,210	C/T	—	uncertain significance
rs2147819095	2:3,623,213	G/A	—	uncertain significance
rs568240834	2:3,623,223	C/T	—	likely benign
rs1661256950	2:3,623,230	C/T	—	uncertain significance
rs1661257045	2:3,623,233	A/C	—	uncertain significance
rs779623517	2:3,623,234	A/G	—	uncertain significance
rs746686516	2:3,623,238	C/T	—	conflicting classifications of pathogenicity
rs2528177015	2:3,623,248	G/C	—	uncertain significance
rs145376788	2:3,623,262	C/T	—	likely benign
rs773617808	2:3,623,265	C/T	—	conflicting classifications of pathogenicity
rs763157114	2:3,623,268	C/T	—	likely benign
rs1661257652	2:3,623,271	C/T	—	likely benign
rs1661257691	2:3,623,275	G/A	—	pathogenic
rs1288683238	2:3,623,282	G/T	—	likely benign
rs751796318	2:3,623,287	C/T	—	likely benign
rs767920442	2:3,623,391	G/A	—	likely benign
rs760614415	2:3,623,394	C/T	—	likely benign
rs2147819267	2:3,623,395	G/C	—	likely benign
rs764256505	2:3,623,399	C/G	—	likely benign
rs750287887	2:3,623,403	T/C	—	likely benign
rs1364756725	2:3,623,404	T/G	—	uncertain significance
rs1057519624	2:3,623,406	G/T	—	pathogenic
rs939123022	2:3,623,408	C/T	—	uncertain significance
rs758369264	2:3,623,410	C/T	—	uncertain significance
rs1661262693	2:3,623,412	T/A	—	likely benign
rs369561705	2:3,623,413	C/T	—	likely benign
rs61732234	2:3,623,430	C/T	—	likely benign
rs754617897	2:3,623,433	G/A	—	likely benign
rs1186234973	2:3,623,436	C/T	—	likely benign
rs929660330	2:3,623,444	C/T	—	uncertain significance
rs2528177481	2:3,623,449	C/G	—	uncertain significance
rs1225711526	2:3,623,451	C/A	—	likely benign
rs777387773	2:3,623,457	G/A	—	likely benign
rs375502460	2:3,623,460	G/A	—	likely benign
rs1661264441	2:3,623,464	A/G	—	uncertain significance
rs1006838420	2:3,623,468	C/T	—	uncertain significance
rs746170084	2:3,623,473	G/T	—	uncertain significance
rs397507554	2:3,623,479	G/A	—	pathogenic
rs1470821464	2:3,623,483	G/C	—	uncertain significance
rs760987417	2:3,623,484	C/T	—	uncertain significance
rs1405210971	2:3,623,485	T/C	—	likely benign
rs2147819351	2:3,623,486	G/A	—	likely benign
rs1381364942	2:3,623,492	C/A	—	likely benign
rs1322963501	2:3,623,493	C/T	—	likely benign
rs912491105	2:3,623,494	C/T	—	likely benign
rs3087873	2:3,623,540	A/G	—	benign
rs11683831	2:3,623,541	G/A	—	benign
rs59077127	2:3,623,555	G/C	—	benign
rs113260758	2:3,623,620	T/A	—	likely benign
rs62106032	2:3,623,883	C/T	—	benign
rs62106033	2:3,623,939	T/C	—	benign
rs797045922	2:3,623,998	G/A	—	uncertain significance
rs62106034	2:3,624,051	C/A	—	benign
rs1661282726	2:3,624,057	A/G	—	likely benign
rs1661282778	2:3,624,058	T/A	—	likely benign
rs533287773	2:3,624,071	C/T	—	conflicting classifications of pathogenicity
rs116840810	2:3,624,078	A/G	missense variant	—
rs1178926489	2:3,624,085	A/C	—	uncertain significance
rs144178741	2:3,624,086	G/A	—	uncertain significance
rs756780024	2:3,624,098	C/T	—	uncertain significance
rs2528178800	2:3,624,106	T/C	—	likely benign
rs922826398	2:3,624,107	A/G	—	uncertain significance
rs1661284278	2:3,624,133	A/G	—	uncertain significance
rs781328965	2:3,624,145	C/T	—	likely benign
rs1434358594	2:3,624,159	T/C	—	uncertain significance
rs1307878805	2:3,624,163	G/T	—	likely benign
rs1267999502	2:3,624,167	G/A	—	uncertain significance
rs760461885	2:3,624,190	C/T	—	likely benign
rs2147819948	2:3,624,192	G/T	—	uncertain significance
rs1244488439	2:3,624,193	T/C	—	likely benign
rs1442216854	2:3,624,202	T/C	—	likely benign
rs61730448	2:3,624,205	C/T	—	likely benign
rs2147819964	2:3,624,206	G/A	—	uncertain significance
rs761597333	2:3,624,211	T/A	—	uncertain significance
rs368931076	2:3,624,214	C/T	—	likely benign
rs748350518	2:3,624,239	C/T	—	likely benign
rs80103345	2:3,624,303	A/G	—	benign
rs75452965	2:3,625,038	T/G	—	benign
rs9808074	2:3,625,067	C/T	—	benign
rs62106037	2:3,625,147	G/C	—	benign
rs72767176	2:3,625,175	T/C	—	benign
rs72767177	2:3,625,179	C/T	—	benign
rs73910594	2:3,625,261	C/T	—	benign
rs150686417	2:3,625,279	A/G	—	likely benign
rs746941533	2:3,625,291	A/T	—	likely benign

Showing 100 of 160 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.