ClinVar Miner

List of variants in gene UBR1 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 38
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HGVS dbSNP gnomAD frequency
NM_174916.3(UBR1):c.1912-94T>A rs7166596 0.98709
NM_174916.3(UBR1):c.4700+12A>G rs2054389 0.85774
NM_174916.3(UBR1):c.4369+124_4369+127dup rs34312632 0.85534
NM_174916.3(UBR1):c.2379+29G>T rs3736054 0.83957
NM_174916.3(UBR1):c.3510-186C>T rs4923955 0.82588
NM_174916.3(UBR1):c.2191-113G>A rs6493077 0.82582
NM_174916.3(UBR1):c.338+172G>T rs12905967 0.82495
NM_174916.3(UBR1):c.2088+63G>A rs3784265 0.80889
NM_174916.3(UBR1):c.*324A>G rs3803341 0.80251
NM_174916.3(UBR1):c.3210-205A>G rs1037990 0.79557
NM_174916.3(UBR1):c.4701-206G>A rs1972447 0.79155
NM_174916.3(UBR1):c.1669-200G>A rs7496079 0.52924
NM_174916.3(UBR1):c.3849-226G>A rs28494835 0.24359
NM_174916.3(UBR1):c.4757+79T>C rs3759792 0.23351
NM_174916.3(UBR1):c.5108+192G>A rs12914380 0.09852
NM_174916.3(UBR1):c.1183-39G>A rs78940367 0.07342
NM_174916.3(UBR1):c.*113G>A rs62020698 0.06222
NM_174916.3(UBR1):c.5205A>G (p.Gln1735=) rs16957277 0.05997
NM_174916.3(UBR1):c.4642A>G (p.Thr1548Ala) rs3917223 0.05280
NM_174916.3(UBR1):c.1282-42A>G rs2035169 0.04921
NM_174916.3(UBR1):c.2585-154T>C rs75465761 0.04180
NM_174916.3(UBR1):c.2940+133A>C rs74009236 0.04092
NM_174916.3(UBR1):c.5108+191C>T rs139986398 0.04010
NM_174916.3(UBR1):c.1668+208G>T rs28605464 0.03691
NM_174916.3(UBR1):c.3028-88C>T rs78688655 0.02853
NM_174916.3(UBR1):c.3997+160G>A rs76783611 0.02462
NM_174916.3(UBR1):c.2190+96A>T rs115199320 0.01988
NM_174916.3(UBR1):c.529-42T>C rs146987997 0.00795
NM_174916.3(UBR1):c.4218+197del rs201655415
NM_174916.3(UBR1):c.4370-132dup rs879184221
NM_174916.3(UBR1):c.4836-53T>C rs2277532
NM_174916.3(UBR1):c.5109-155_5109-146del rs58543903
NM_174916.3(UBR1):c.660-149del rs545130203
NM_174916.3(UBR1):c.660-71dup rs375762522
NM_174916.3(UBR1):c.82-216dup rs370942763
NM_174916.3(UBR1):c.985+113del rs36021315
NM_174916.3(UBR1):c.985+97_985+100del rs770035678
NM_174916.3(UBR1):c.985+97_985+99del rs757569234

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