ClinVar Miner

List of variants in gene DNAJC6 reported as uncertain significance for juvenile-onset Parkinson disease

Included ClinVar conditions (7):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 89
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001256864.2(DNAJC6):c.397A>T (p.Met133Leu) rs61757223 0.00046
NM_001256864.2(DNAJC6):c.829G>A (p.Ala277Thr) rs146050826 0.00045
NM_001256864.2(DNAJC6):c.1113G>A (p.Lys371=) rs144924736 0.00022
NM_001256864.2(DNAJC6):c.1070T>C (p.Met357Thr) rs201840876 0.00015
NM_001256864.2(DNAJC6):c.1039A>G (p.Ile347Val) rs200712827 0.00012
NM_001256864.2(DNAJC6):c.1832C>T (p.Ala611Val) rs375368522 0.00011
NM_001256864.2(DNAJC6):c.992T>C (p.Met331Thr) rs760136045 0.00009
NM_001256864.2(DNAJC6):c.1715C>T (p.Ala572Val) rs141779215 0.00007
NM_001256864.2(DNAJC6):c.1607A>G (p.Lys536Arg) rs376992397 0.00006
NM_001256864.2(DNAJC6):c.674G>A (p.Arg225Gln) rs772437036 0.00006
NM_001256864.2(DNAJC6):c.844C>T (p.Arg282Cys) rs141833490 0.00005
NM_001256864.2(DNAJC6):c.119G>T (p.Arg40Ile) rs754115488 0.00004
NM_001256864.2(DNAJC6):c.1852C>T (p.Arg618Cys) rs377366345 0.00004
NM_001256864.2(DNAJC6):c.2212G>A (p.Asp738Asn) rs140156759 0.00004
NM_001256864.2(DNAJC6):c.2443G>T (p.Ala815Ser) rs369274494 0.00004
NM_001256864.2(DNAJC6):c.2839G>A (p.Ala947Thr) rs755391548 0.00004
NM_001256864.2(DNAJC6):c.677C>T (p.Ala226Val) rs776225529 0.00003
NM_001256864.2(DNAJC6):c.926G>A (p.Arg309His) rs757458350 0.00003
NM_001256864.2(DNAJC6):c.1709C>T (p.Pro570Leu) rs751850074 0.00002
NM_001256864.2(DNAJC6):c.175A>G (p.Ser59Gly) rs1296532855 0.00002
NM_001256864.2(DNAJC6):c.1990A>G (p.Ser664Gly) rs986073706 0.00002
NM_001256864.2(DNAJC6):c.2044A>G (p.Ser682Gly) rs145175543 0.00002
NM_001256864.2(DNAJC6):c.2072A>G (p.Asp691Gly) rs747034717 0.00002
NM_001256864.2(DNAJC6):c.344+4C>T rs561389842 0.00002
NM_001256864.2(DNAJC6):c.518A>G (p.Tyr173Cys) rs1428381539 0.00002
NM_001256864.2(DNAJC6):c.101G>C (p.Gly34Ala) rs956622990 0.00001
NM_001256864.2(DNAJC6):c.154C>G (p.Arg52Gly) rs547312338 0.00001
NM_001256864.2(DNAJC6):c.1646C>T (p.Pro549Leu) rs1230286867 0.00001
NM_001256864.2(DNAJC6):c.170G>T (p.Arg57Leu) rs747115530 0.00001
NM_001256864.2(DNAJC6):c.1716G>A (p.Ala572=) rs201766287 0.00001
NM_001256864.2(DNAJC6):c.1877C>T (p.Ala626Val) rs761922985 0.00001
NM_001256864.2(DNAJC6):c.2003T>A (p.Leu668His) rs1363537326 0.00001
NM_001256864.2(DNAJC6):c.2020C>T (p.Pro674Ser) rs749594846 0.00001
NM_001256864.2(DNAJC6):c.2086T>C (p.Trp696Arg) rs1462099424 0.00001
NM_001256864.2(DNAJC6):c.2107+3A>G rs371583880 0.00001
NM_001256864.2(DNAJC6):c.2228-3T>C rs753885398 0.00001
NM_001256864.2(DNAJC6):c.224A>G (p.Tyr75Cys) rs1394529150 0.00001
NM_001256864.2(DNAJC6):c.2290C>T (p.Leu764Phe) rs917235831 0.00001
NM_001256864.2(DNAJC6):c.2468G>A (p.Arg823His) rs201984806 0.00001
NM_001256864.2(DNAJC6):c.2762A>T (p.Gln921Leu) rs1203943853 0.00001
NM_001256864.2(DNAJC6):c.2873G>T (p.Trp958Leu) rs1380186979 0.00001
NM_001256864.2(DNAJC6):c.521G>A (p.Arg174Gln) rs895749847 0.00001
NM_001256864.2(DNAJC6):c.833A>G (p.Asp278Gly) rs368290134 0.00001
NC_000001.10:g.(?_65775429)_(65831899_?)dup
NC_000001.10:g.(?_65849856)_(65855330_?)dup
NC_000001.10:g.(?_65853999)_(65878708_?)dup
NM_001256864.2(DNAJC6):c.1012G>C (p.Asp338His)
NM_001256864.2(DNAJC6):c.128C>T (p.Ala43Val)
NM_001256864.2(DNAJC6):c.1348T>G (p.Ser450Ala) rs1645902989
NM_001256864.2(DNAJC6):c.1388-18G>A
NM_001256864.2(DNAJC6):c.1446C>A (p.Phe482Leu) rs1645906223
NM_001256864.2(DNAJC6):c.149C>T (p.Pro50Leu)
NM_001256864.2(DNAJC6):c.1504C>T (p.His502Tyr)
NM_001256864.2(DNAJC6):c.164C>A (p.Pro55Gln) rs916872480
NM_001256864.2(DNAJC6):c.1651C>A (p.Pro551Thr) rs377495314
NM_001256864.2(DNAJC6):c.1666C>T (p.Leu556Phe) rs1262741318
NM_001256864.2(DNAJC6):c.1741C>G (p.Leu581Val)
NM_001256864.2(DNAJC6):c.1794G>C (p.Gln598His) rs2101614376
NM_001256864.2(DNAJC6):c.1817A>C (p.His606Pro) rs199937139
NM_001256864.2(DNAJC6):c.1819C>A (p.Pro607Thr)
NM_001256864.2(DNAJC6):c.1831G>A (p.Ala611Thr) rs1015326337
NM_001256864.2(DNAJC6):c.1841A>G (p.Gln614Arg)
NM_001256864.2(DNAJC6):c.1856G>A (p.Arg619His) rs139509177
NM_001256864.2(DNAJC6):c.1894G>C (p.Val632Leu)
NM_001256864.2(DNAJC6):c.1982G>A (p.Ser661Asn) rs2101618114
NM_001256864.2(DNAJC6):c.2038+3A>G rs961974767
NM_001256864.2(DNAJC6):c.2106A>G (p.Pro702=)
NM_001256864.2(DNAJC6):c.2107+8_2107+10del rs1199919797
NM_001256864.2(DNAJC6):c.2119A>G (p.Met707Val)
NM_001256864.2(DNAJC6):c.2255C>T (p.Thr752Ile) rs2101635055
NM_001256864.2(DNAJC6):c.2309C>T (p.Ala770Val)
NM_001256864.2(DNAJC6):c.2351C>T (p.Ala784Val)
NM_001256864.2(DNAJC6):c.2468G>C (p.Arg823Pro) rs201984806
NM_001256864.2(DNAJC6):c.2476G>A (p.Gly826Arg)
NM_001256864.2(DNAJC6):c.2506G>T (p.Ala836Ser)
NM_001256864.2(DNAJC6):c.2553C>G (p.His851Gln)
NM_001256864.2(DNAJC6):c.2594A>G (p.Lys865Arg)
NM_001256864.2(DNAJC6):c.2689A>T (p.Met897Leu)
NM_001256864.2(DNAJC6):c.2715G>C (p.Glu905Asp) rs201708707
NM_001256864.2(DNAJC6):c.2846T>C (p.Met949Thr)
NM_001256864.2(DNAJC6):c.32C>T (p.Thr11Ile) rs2101357416
NM_001256864.2(DNAJC6):c.344+6C>T
NM_001256864.2(DNAJC6):c.542G>A (p.Arg181Gln)
NM_001256864.2(DNAJC6):c.700G>A (p.Ala234Thr)
NM_001256864.2(DNAJC6):c.79G>T (p.Asp27Tyr)
NM_001256864.2(DNAJC6):c.809G>A (p.Gly270Asp) rs1645865223
NM_001256864.2(DNAJC6):c.839C>T (p.Pro280Leu) rs774319050
NM_001256864.2(DNAJC6):c.83T>C (p.Leu28Ser)
NM_001256864.2(DNAJC6):c.973T>C (p.Cys325Arg) rs1436860964

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.