WDSUB1

WD repeat, sterile alpha motif and U-box domain containing 1

Summary

Predicted to enable ubiquitin-protein transferase activity. Predicted to be involved in protein ubiquitination. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants31 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs1000148310	2:160,092,555	G/A	—	uncertain significance
rs202103797	2:160,092,572	T/C	—	uncertain significance
rs144493205	2:160,092,593	C/G	—	uncertain significance
rs780664239	2:160,092,611	G/A	—	likely benign
rs7573782	2:160,102,681	C/T	intron variant	—
rs758437110	2:160,104,897	G/A	—	uncertain significance
rs2060870609	2:160,104,937	C/T	—	uncertain significance
rs2470426782	2:160,112,731	T/G	—	uncertain significance
rs2470427194	2:160,112,757	T/C	—	likely benign
rs138625384	2:160,112,772	T/C	—	uncertain significance
rs201147705	2:160,112,883	C/G	—	uncertain significance
rs141839163	2:160,113,477	C/A	intron variant	—
rs139910347	2:160,114,308	C/T	—	uncertain significance
rs752424863	2:160,116,335	T/C	—	uncertain significance
rs35074746	2:160,125,665	T/C	intron variant	—
rs1335844256	2:160,128,223	G/C	—	uncertain significance
rs149594738	2:160,128,291	T/C	—	uncertain significance
rs745416660	2:160,136,404	C/T	—	uncertain significance
rs13026565	2:160,137,169	T/C	intron variant	—
rs377519164	2:160,139,252	G/A	—	uncertain significance
rs890827934	2:160,139,277	C/T	—	uncertain significance
rs775641046	2:160,139,294	C/G	—	uncertain significance
rs765068662	2:160,139,306	A/C	—	uncertain significance
rs1265732449	2:160,139,381	T/A	—	uncertain significance
rs2470632153	2:160,139,444	G/A	—	uncertain significance
rs766094209	2:160,139,463	G/T	—	likely benign
rs757712542	2:160,139,478	G/A	—	uncertain significance
rs749197258	2:160,139,540	T/C	—	uncertain significance
rs775150156	2:160,139,559	A/C	—	uncertain significance
rs78712300	2:160,141,997	A/T	intron variant	—
rs35349053	2:160,144,134	G/T	—	—

Gene information from NCBI Gene. Variant classifications from ClinVar.