ClinVar Miner

List of variants reported as likely benign for X-linked intellectual disability Cabezas type

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 54
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001079872.2(CUL4B):c.1857C>T (p.Cys619=) rs148700620 0.00099
NM_001079872.2(CUL4B):c.319C>G (p.Leu107Val) rs760294805 0.00011
NM_003588.4(CUL4B):c.67+10T>C rs992197854 0.00011
NM_001079872.2(CUL4B):c.776+12A>G rs112085497 0.00006
NM_001079872.2(CUL4B):c.139A>G (p.Ser47Gly) rs145134351 0.00005
NM_001079872.2(CUL4B):c.672+13A>G rs372394678 0.00005
NM_001079872.2(CUL4B):c.776+13A>G rs781274909 0.00005
NM_001079872.2(CUL4B):c.920+9G>A rs375607970 0.00005
NM_001079872.2(CUL4B):c.954T>C (p.Ile318=) rs144312827 0.00005
NM_001079872.2(CUL4B):c.1305A>T (p.Leu435Phe) rs886043694 0.00003
NM_001079872.2(CUL4B):c.573A>G (p.Pro191=) rs776364726 0.00003
NM_001079872.2(CUL4B):c.1674A>G (p.Lys558=) rs1017138439 0.00002
NM_001079872.2(CUL4B):c.1722C>T (p.Ile574=) rs142211300 0.00002
NM_001079872.2(CUL4B):c.1939-4A>G rs1405740580 0.00002
NM_001079872.2(CUL4B):c.1071G>A (p.Leu357=) rs985263401 0.00001
NM_001079872.2(CUL4B):c.1324+9C>A rs751888920 0.00001
NM_001079872.2(CUL4B):c.1392A>G (p.Arg464=) rs749131350 0.00001
NM_001079872.2(CUL4B):c.1444-4T>G rs766196936 0.00001
NM_001079872.2(CUL4B):c.228A>G (p.Ala76=) rs972696850 0.00001
NM_001079872.2(CUL4B):c.2322T>G (p.Val774=) rs1186093103 0.00001
NM_001079872.2(CUL4B):c.2593-18A>C rs1297445532 0.00001
NM_001079872.2(CUL4B):c.270T>C (p.Ala90=) rs371312556 0.00001
NM_001079872.2(CUL4B):c.510C>T (p.Asn170=) rs758768060 0.00001
NM_001079872.2(CUL4B):c.557-11A>G rs776962581 0.00001
NM_001079872.2(CUL4B):c.69C>T (p.Ala23=) rs1229501675 0.00001
NM_001079872.2(CUL4B):c.95C>T (p.Pro32Leu) rs869320682 0.00001
NM_001079872.2(CUL4B):c.1044T>C (p.Ser348=) rs1924202904
NM_001079872.2(CUL4B):c.1173+16G>A rs2521120464
NM_001079872.2(CUL4B):c.1256+18A>T rs2521118363
NM_001079872.2(CUL4B):c.1338C>A (p.Leu446=)
NM_001079872.2(CUL4B):c.1389T>C (p.Ser463=) rs2521106591
NM_001079872.2(CUL4B):c.1396C>A (p.Arg466=)
NM_001079872.2(CUL4B):c.1452C>G (p.Gly484=) rs1464061635
NM_001079872.2(CUL4B):c.15T>C (p.Gly5=) rs2521201964
NM_001079872.2(CUL4B):c.2118G>A (p.Gln706=) rs2521075353
NM_001079872.2(CUL4B):c.2160+8G>A rs2521075055
NM_001079872.2(CUL4B):c.2280A>G (p.Leu760=)
NM_001079872.2(CUL4B):c.2290C>T (p.Leu764=) rs2521057313
NM_001079872.2(CUL4B):c.2439+11C>A rs1923372277
NM_001079872.2(CUL4B):c.243G>T (p.Ser81=) rs1478158662
NM_001079872.2(CUL4B):c.2593-16T>C
NM_001079872.2(CUL4B):c.360CTC[5] (p.Ser128del) rs754330779
NM_001079872.2(CUL4B):c.360CTC[7] (p.Ser128dup) rs754330779
NM_001079872.2(CUL4B):c.378A>C (p.Ser126=) rs1022353335
NM_001079872.2(CUL4B):c.53A>G (p.Gln18Arg) rs1199433297
NM_001079872.2(CUL4B):c.556+9G>C rs1352392886
NM_001079872.2(CUL4B):c.672+18T>C rs1925074883
NM_001079872.2(CUL4B):c.673-10A>G
NM_001079872.2(CUL4B):c.777-11A>G rs1924348219
NM_001079872.2(CUL4B):c.783A>G (p.Ser261=) rs113566433
NM_001079872.2(CUL4B):c.843A>G (p.Gln281=)
NM_001079872.2(CUL4B):c.847-10del rs762094686
NM_001079872.2(CUL4B):c.90C>T (p.Thr30=)
NM_001079872.2(CUL4B):c.984A>G (p.Thr328=) rs2521123725

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.