ClinVar Miner

List of variants in gene DNAJC6 reported as uncertain significance for basal ganglia disorder

Included ClinVar conditions (83):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 87
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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.(?_65849856)_(65855330_?)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

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