TDRD9

tudor domain containing 9

Summary

Predicted to enable ATP hydrolysis activity; RNA binding activity; and helicase activity. Involved in spermatogenesis. Located in cytoplasm and nucleus. Implicated in spermatogenic failure 30. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants122 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs868220412	14:104,394,892	A/C	—	uncertain significance
rs1294873202	14:104,394,895	G/T	—	uncertain significance
rs569772232	14:104,394,944	C/T	—	uncertain significance
rs1049310223	14:104,394,956	C/T	—	uncertain significance
rs1007417173	14:104,394,985	G/T	—	uncertain significance
rs867213957	14:104,394,990	C/T	—	likely benign
rs1162535637	14:104,394,998	G/A	—	uncertain significance
rs979526397	14:104,395,040	G/A	—	uncertain significance
rs992290495	14:104,395,052	C/T	—	uncertain significance
rs10220464	14:104,403,155	A/G	downstream gene variant	—
rs755011079	14:104,422,077	T/G	—	uncertain significance
rs77852716	14:104,422,080	C/T	—	uncertain significance
rs753182841	14:104,422,081	G/T	—	uncertain significance
rs2032163186	14:104,422,102	G/A	—	uncertain significance
rs73352472	14:104,429,406	C/T	—	benign
rs77260485	14:104,429,425	C/T	—	conflicting classifications of pathogenicity
rs532678979	14:104,431,667	T/C	—	likely benign
rs1323254659	14:104,431,685	G/C	—	uncertain significance
rs752708200	14:104,431,697	G/A	—	uncertain significance
rs201249896	14:104,431,780	C/T	—	likely benign
rs552190625	14:104,431,811	C/T	—	uncertain significance
rs936600145	14:104,431,848	G/T	—	uncertain significance
rs2032701619	14:104,431,873	A/T	—	likely benign
rs2032703166	14:104,431,899	T/G	—	likely benign
rs142035530	14:104,433,097	A/G	—	benign
rs2510961139	14:104,433,106	C/G	—	uncertain significance
rs1171512069	14:104,433,143	A/G	—	uncertain significance
rs776156806	14:104,436,887	C/T	—	pathogenic
rs747643848	14:104,436,924	G/A	—	uncertain significance
rs1196971698	14:104,436,932	T/G	—	uncertain significance
rs1043899460	14:104,436,948	G/A	—	uncertain significance
rs10141374	14:104,437,920	T/C	intron variant	—
rs770570537	14:104,441,735	A/T	—	uncertain significance
rs147103471	14:104,441,786	G/C	—	benign
rs764483040	14:104,441,810	T/C	—	uncertain significance
rs202227961	14:104,441,846	G/A	—	uncertain significance
rs770073563	14:104,452,561	C/A	—	uncertain significance
rs150241317	14:104,452,564	A/G	—	uncertain significance
rs540412831	14:104,452,645	T/C	—	likely benign
rs1275444344	14:104,457,514	G/C	—	uncertain significance
rs769592233	14:104,460,689	A/C	—	uncertain significance
rs2511050390	14:104,460,722	A/G	—	uncertain significance
rs756953745	14:104,460,863	G/T	—	uncertain significance
rs1352745082	14:104,460,930	G/T	—	uncertain significance
rs531774714	14:104,465,024	G/A	—	uncertain significance
rs144585440	14:104,470,602	A/G	—	uncertain significance
rs187586531	14:104,470,628	T/G	—	uncertain significance
rs372987923	14:104,471,642	T/A	—	uncertain significance
rs761368542	14:104,471,649	A/T	—	uncertain significance
rs753553775	14:104,471,683	A/G	—	uncertain significance
rs2511098189	14:104,471,702	G/T	—	uncertain significance
rs202014262	14:104,471,720	G/A	—	uncertain significance
rs1347119849	14:104,472,819	G/A	—	uncertain significance
rs374185759	14:104,473,024	C/T	—	uncertain significance
rs375856681	14:104,473,025	G/A	—	uncertain significance
rs35030451	14:104,473,128	G/A	—	likely benign
rs369524968	14:104,473,530	C/T	—	uncertain significance
rs752318349	14:104,473,531	G/A	—	uncertain significance
rs1290516824	14:104,473,537	C/T	—	uncertain significance
rs2152222013	14:104,474,805	T/A	—	uncertain significance
rs757739389	14:104,481,099	C/T	—	uncertain significance
rs545124595	14:104,481,123	C/T	—	uncertain significance
rs764347895	14:104,481,165	G/A	—	uncertain significance
rs570254371	14:104,481,181	G/A	—	likely benign
rs745509162	14:104,482,381	G/A	—	uncertain significance
rs2152232457	14:104,482,414	A/G	—	uncertain significance
rs1243714748	14:104,484,465	A/G	—	uncertain significance
rs2511157412	14:104,484,467	A/T	—	uncertain significance
rs1595991965	14:104,484,503	C/T	—	likely benign
rs372317574	14:104,488,501	G/A	—	uncertain significance
rs202130253	14:104,490,901	T/C	—	benign
rs559335049	14:104,490,987	A/G	—	likely benign
rs372923737	14:104,491,896	T/G	—	likely benign
rs765299197	14:104,491,925	G/A	—	uncertain significance
rs35463712	14:104,491,990	G/C	—	benign
rs367638250	14:104,492,065	A/C	—	uncertain significance
rs2511189203	14:104,492,103	A/G	—	uncertain significance
rs201873918	14:104,492,406	A/G	—	uncertain significance
rs2035107979	14:104,492,416	T/G	—	uncertain significance
rs774458228	14:104,492,421	A/G	—	uncertain significance
rs766366437	14:104,492,441	A/G	—	uncertain significance
rs2511191508	14:104,492,442	T/G	—	uncertain significance
rs373060575	14:104,493,052	G/A	—	uncertain significance
rs150591179	14:104,493,112	C/T	—	likely benign
rs35169220	14:104,493,171	C/T	—	benign
rs750015527	14:104,493,255	G/A	—	likely benign
rs2511214294	14:104,497,505	T/C	—	uncertain significance
rs147169550	14:104,497,532	G/A	—	uncertain significance
rs1054416423	14:104,497,574	A/G	—	uncertain significance
rs978562376	14:104,497,581	T/C	—	uncertain significance
rs2035299158	14:104,498,405	A/G	—	uncertain significance
rs148393162	14:104,498,428	T/C	—	benign
rs76761167	14:104,500,301	A/G	—	likely benign
rs1596016269	14:104,501,302	A/G	—	uncertain significance
rs550509205	14:104,501,303	C/T	—	uncertain significance
rs536343348	14:104,501,338	A/C	—	uncertain significance
rs1336788927	14:104,501,351	C/T	—	uncertain significance
rs147205456	14:104,501,384	T/C	—	uncertain significance
rs773919914	14:104,501,396	A/G	—	likely pathogenic
rs1195605404	14:104,506,618	C/A	—	uncertain significance

Showing 100 of 122 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.