ClinVar Miner

List of variants in gene DNAJC6 reported as likely benign for juvenile-onset Parkinson disease

Included ClinVar conditions (7):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 69
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HGVS dbSNP gnomAD frequency
NM_001256864.2(DNAJC6):c.194-20_194-19insG rs111346712 0.03019
NM_001256864.2(DNAJC6):c.1456C>T (p.Leu486Phe) rs78141380 0.01170
NM_001256864.2(DNAJC6):c.194-5G>T rs753576283 0.00359
NM_001256864.2(DNAJC6):c.194-18T>G rs201249130 0.00252
NM_001256864.2(DNAJC6):c.1492T>A (p.Cys498Ser) rs145329294 0.00237
NM_001256864.2(DNAJC6):c.2254A>T (p.Thr752Ser) rs113143702 0.00201
NM_001256864.2(DNAJC6):c.194-16T>G rs772643958 0.00119
NM_001256864.2(DNAJC6):c.2159C>T (p.Ser720Leu) rs143504255 0.00116
NM_001256864.2(DNAJC6):c.198C>T (p.Ala66=) rs374727491 0.00030
NM_001256864.2(DNAJC6):c.1182A>G (p.Leu394=) rs148145327 0.00015
NM_001256864.2(DNAJC6):c.1577A>G (p.Asn526Ser) rs191459935 0.00015
NM_001256864.2(DNAJC6):c.216G>A (p.Glu72=) rs146062011 0.00013
NM_001256864.2(DNAJC6):c.2298G>A (p.Ser766=) rs540477402 0.00010
NM_001256864.2(DNAJC6):c.2463C>T (p.Asn821=) rs193114909 0.00009
NM_001256864.2(DNAJC6):c.2697C>T (p.Thr899=) rs149097758 0.00009
NM_001256864.2(DNAJC6):c.1194-9C>G rs370864885 0.00005
NM_001256864.2(DNAJC6):c.264G>A (p.Gly88=) rs139946043 0.00005
NM_001256864.2(DNAJC6):c.2838C>T (p.Tyr946=) rs148209150 0.00005
NM_001256864.2(DNAJC6):c.1350T>C (p.Ser450=) rs202109326 0.00004
NM_001256864.2(DNAJC6):c.1374G>A (p.Thr458=) rs148673423 0.00004
NM_001256864.2(DNAJC6):c.186C>T (p.Asp62=) rs371984320 0.00004
NM_001256864.2(DNAJC6):c.2310G>A (p.Ala770=) rs113490907 0.00004
NM_001256864.2(DNAJC6):c.2526A>G (p.Leu842=) rs753691766 0.00004
NM_001256864.2(DNAJC6):c.144G>T (p.Arg48=) rs779540362 0.00003
NM_001256864.2(DNAJC6):c.1904-12A>G rs774888599 0.00003
NM_001256864.2(DNAJC6):c.1533G>A (p.Glu511=) rs773744229 0.00002
NM_001256864.2(DNAJC6):c.2151C>T (p.Thr717=) rs145501615 0.00002
NM_001256864.2(DNAJC6):c.1755T>C (p.Phe585=) rs1412214392 0.00001
NM_001256864.2(DNAJC6):c.2223A>T (p.Thr741=) rs879255554 0.00001
NM_001256864.2(DNAJC6):c.751T>C (p.Leu251=) rs755098010 0.00001
NM_001256864.2(DNAJC6):c.897C>G (p.Pro299=) rs371261372 0.00001
NM_001256864.2(DNAJC6):c.117G>A (p.Gln39=)
NM_001256864.2(DNAJC6):c.1185G>A (p.Lys395=)
NM_001256864.2(DNAJC6):c.1269G>A (p.Gln423=) rs2101607355
NM_001256864.2(DNAJC6):c.1383A>G (p.Leu461=)
NM_001256864.2(DNAJC6):c.1431C>T (p.Tyr477=)
NM_001256864.2(DNAJC6):c.1569G>A (p.Pro523=)
NM_001256864.2(DNAJC6):c.156A>G (p.Arg52=)
NM_001256864.2(DNAJC6):c.1662G>A (p.Val554=)
NM_001256864.2(DNAJC6):c.1824T>C (p.Ser608=)
NM_001256864.2(DNAJC6):c.1845A>G (p.Ser615=) rs2101614479
NM_001256864.2(DNAJC6):c.194-13T>G rs765899995
NM_001256864.2(DNAJC6):c.194-15T>G
NM_001256864.2(DNAJC6):c.1974C>T (p.Asn658=)
NM_001256864.2(DNAJC6):c.2025G>T (p.Ser675=) rs185245369
NM_001256864.2(DNAJC6):c.2039-4G>T
NM_001256864.2(DNAJC6):c.2107+11G>T
NM_001256864.2(DNAJC6):c.210C>T (p.Asp70=)
NM_001256864.2(DNAJC6):c.2130G>A (p.Lys710=)
NM_001256864.2(DNAJC6):c.2205T>G (p.Pro735=)
NM_001256864.2(DNAJC6):c.2228-17T>A rs2101634939
NM_001256864.2(DNAJC6):c.2235T>C (p.Ser745=)
NM_001256864.2(DNAJC6):c.2370A>C (p.Pro790=)
NM_001256864.2(DNAJC6):c.2634+18C>T
NM_001256864.2(DNAJC6):c.2643A>G (p.Glu881=)
NM_001256864.2(DNAJC6):c.270C>T (p.Leu90=)
NM_001256864.2(DNAJC6):c.2790C>T (p.Val930=)
NM_001256864.2(DNAJC6):c.2799G>A (p.Val933=) rs764156036
NM_001256864.2(DNAJC6):c.344+12C>T
NM_001256864.2(DNAJC6):c.507A>G (p.Ser169=) rs2101558882
NM_001256864.2(DNAJC6):c.543+10T>G
NM_001256864.2(DNAJC6):c.666+10C>G rs373591833
NM_001256864.2(DNAJC6):c.750A>T (p.Arg250=) rs2101597985
NM_001256864.2(DNAJC6):c.789A>T (p.Pro263=)
NM_001256864.2(DNAJC6):c.801-14A>C rs758557034
NM_001256864.2(DNAJC6):c.876G>A (p.Ser292=)
NM_001256864.2(DNAJC6):c.995+16T>C rs1254823370
NM_001256864.2(DNAJC6):c.996-14G>T
NM_001256864.2(DNAJC6):c.996-15G>T

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