ClinVar Miner

List of variants in gene DNAJC5 reported as benign for brain disorder

Included ClinVar conditions (1840):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 63
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_025219.3(DNAJC5):c.*2912C>T rs749723 0.17505
NM_025219.3(DNAJC5):c.*1442A>G rs61744085 0.08435
NM_025219.3(DNAJC5):c.*1648C>T rs41278222 0.08304
NM_025219.3(DNAJC5):c.*2711G>A rs76291580 0.08294
NM_025219.3(DNAJC5):c.*1106T>G rs11554629 0.08271
NM_025219.3(DNAJC5):c.*2701C>T rs3206771 0.08172
NM_025219.3(DNAJC5):c.321+20C>T rs2295436 0.07912
NM_025219.3(DNAJC5):c.322-10C>T rs78457562 0.07717
NM_025219.3(DNAJC5):c.*1303C>T rs41278214 0.06711
NM_025219.3(DNAJC5):c.*2725G>A rs11554628 0.06691
NM_025219.3(DNAJC5):c.*2208C>T rs11554631 0.06117
NM_025219.3(DNAJC5):c.*2601C>T rs112103063 0.06085
NM_025219.3(DNAJC5):c.*4007G>C rs77777268 0.02556
NM_025219.3(DNAJC5):c.*4385A>T rs77335831 0.01815
NM_025219.3(DNAJC5):c.*4300C>T rs41278224 0.01781
NM_025219.3(DNAJC5):c.144C>T (p.Pro48=) rs113987077 0.01342
NM_025219.3(DNAJC5):c.*3670A>G rs77107548 0.01329
NM_025219.3(DNAJC5):c.*4117C>T rs11554630 0.01268
NM_025219.3(DNAJC5):c.*895C>G rs1064345 0.01026
NM_025219.3(DNAJC5):c.*2878T>C rs749724 0.00565
NM_025219.3(DNAJC5):c.*817C>T rs114525694 0.00491
NM_025219.3(DNAJC5):c.*1364C>T rs61735744 0.00449
NM_025219.3(DNAJC5):c.*909G>T rs114038171 0.00395
NM_025219.3(DNAJC5):c.*1235C>T rs149675982 0.00347
NM_025219.3(DNAJC5):c.*1342G>A rs41278218 0.00334
NM_025219.3(DNAJC5):c.132C>T (p.Pro44=) rs140948457 0.00314
NM_025219.3(DNAJC5):c.*3204C>T rs140377993 0.00248
NM_025219.3(DNAJC5):c.*1820C>A rs182604967 0.00237
NM_025219.3(DNAJC5):c.*1183G>T rs562364964 0.00208
NM_025219.3(DNAJC5):c.*750G>T rs140106848 0.00140
NM_025219.3(DNAJC5):c.*195G>A rs180676568 0.00135
NM_025219.3(DNAJC5):c.456C>T (p.Pro152=) rs140326040 0.00130
NM_025219.3(DNAJC5):c.*1433G>A rs41278220 0.00125
NM_025219.3(DNAJC5):c.*1556A>G rs58526294 0.00108
NM_025219.3(DNAJC5):c.*3269C>G rs528394634 0.00107
NM_025219.3(DNAJC5):c.*2218A>G rs142121195 0.00106
NM_025219.3(DNAJC5):c.*2790C>T rs55665472 0.00101
NM_025219.3(DNAJC5):c.107+10C>T rs181906972 0.00101
NM_025219.3(DNAJC5):c.*4006C>T rs138866062 0.00079
NM_025219.3(DNAJC5):c.*4065G>A rs373099874 0.00076
NM_025219.3(DNAJC5):c.107+12A>G rs372843187 0.00074
NM_025219.3(DNAJC5):c.*2039C>T rs79245733 0.00073
NM_025219.3(DNAJC5):c.*3413A>G rs150408300 0.00071
NM_025219.3(DNAJC5):c.45A>G (p.Ser15=) rs144141585 0.00066
NM_025219.3(DNAJC5):c.*1630C>T rs527390994 0.00050
NM_025219.3(DNAJC5):c.*4129G>C rs191412647 0.00034
NM_025219.3(DNAJC5):c.*4131C>T rs146360147 0.00032
NM_025219.3(DNAJC5):c.228C>T (p.Tyr76=) rs201495666 0.00031
NM_025219.3(DNAJC5):c.*3432G>A rs1051821 0.00016
NM_025219.3(DNAJC5):c.75C>T (p.Asn25=) rs189308547 0.00010
NM_025219.3(DNAJC5):c.*728G>A rs150670642 0.00008
NM_025219.3(DNAJC5):c.*1079T>C rs370539010 0.00006
NM_025219.3(DNAJC5):c.*2563A>C rs188604040 0.00006
NM_025219.3(DNAJC5):c.*1643T>C rs142546412 0.00005
NM_025219.3(DNAJC5):c.108-3C>T rs541118679 0.00004
NM_025219.3(DNAJC5):c.*1604C>T rs554749952 0.00001
NM_025219.3(DNAJC5):c.*1936T>C rs574966040 0.00001
NM_025219.3(DNAJC5):c.*2723A>G rs76769576
NM_025219.3(DNAJC5):c.*4070C>G rs3810500
NM_025219.3(DNAJC5):c.*727C>A rs75130625
NM_025219.3(DNAJC5):c.*727C>G rs75130625
NM_025219.3(DNAJC5):c.*853C>G rs6011230
NM_025219.3(DNAJC5):c.322-3dup rs1173184036

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.