ClinVar Miner

List of variants in gene DNAJC19 reported as likely benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_145261.4(DNAJC19):c.130-292T>C rs1805637 0.02945
NM_145261.4(DNAJC19):c.4-128_4-127insG rs766807321 0.01035
NM_145261.4(DNAJC19):c.285A>C (p.Gly95=) rs17850540 0.00755
NM_145261.4(DNAJC19):c.281-160A>T rs139914001 0.00525
NM_145261.4(DNAJC19):c.280+129G>A rs115056126 0.00503
NM_145261.4(DNAJC19):c.69G>A (p.Leu23=) rs142023670 0.00321
NM_145261.4(DNAJC19):c.-29G>T rs181271620 0.00089
NM_145261.4(DNAJC19):c.300A>G (p.Ala100=) rs373886730 0.00044
NM_145261.4(DNAJC19):c.331G>C (p.Glu111Gln) rs370042988 0.00024
NM_145261.4(DNAJC19):c.182G>A (p.Arg61Gln) rs376891597 0.00016
NM_145261.4(DNAJC19):c.3+16C>T rs367841424 0.00013
NM_145261.4(DNAJC19):c.129+15A>C rs201697391 0.00010
NM_145261.4(DNAJC19):c.280+2dup rs756616792 0.00007
NM_145261.4(DNAJC19):c.181C>T (p.Arg61Trp) rs141007488 0.00004
NM_145261.4(DNAJC19):c.333A>G (p.Glu111=) rs766348961 0.00003
NM_145261.4(DNAJC19):c.59G>A (p.Arg20His) rs756192515 0.00003
NM_145261.4(DNAJC19):c.210-17T>C rs750700018 0.00002
NM_145261.4(DNAJC19):c.90G>A (p.Glu30=) rs367996239 0.00002
NM_145261.4(DNAJC19):c.105A>G (p.Gln35=) rs1400868784 0.00001
NM_145261.4(DNAJC19):c.111T>C (p.Phe37=) rs2473933568 0.00001
NM_145261.4(DNAJC19):c.120A>T (p.Leu40=) rs1476161168 0.00001
NM_145261.4(DNAJC19):c.129+11G>T rs546533068 0.00001
NM_145261.4(DNAJC19):c.150T>C (p.Tyr50=) rs1714944777 0.00001
NM_145261.4(DNAJC19):c.159G>C (p.Gly53=) rs751736236 0.00001
NM_145261.4(DNAJC19):c.210-12T>A rs1203551473 0.00001
NM_145261.4(DNAJC19):c.210-18A>G rs758730746 0.00001
NM_145261.4(DNAJC19):c.210-19C>T rs780397593 0.00001
NM_145261.4(DNAJC19):c.280+15A>C rs1714878433 0.00001
NM_145261.4(DNAJC19):c.281-4A>T rs1256818835 0.00001
NM_145261.4(DNAJC19):c.348A>G (p.Lys116=) rs771098271 0.00001
NM_145261.4(DNAJC19):c.84T>C (p.His28=) rs768399273 0.00001
NM_145261.4(DNAJC19):c.129+7C>T rs2108509597
NM_145261.4(DNAJC19):c.129T>C (p.Ser43=) rs2473933488
NM_145261.4(DNAJC19):c.130-38_130-34del rs145145539
NM_145261.4(DNAJC19):c.130-4T>C rs771851624
NM_145261.4(DNAJC19):c.132C>G (p.Ala44=)
NM_145261.4(DNAJC19):c.192A>G (p.Ala64=) rs1473896211
NM_145261.4(DNAJC19):c.209+11C>T rs374496383
NM_145261.4(DNAJC19):c.209+19T>C rs2473930142
NM_145261.4(DNAJC19):c.209+95C>G rs192120432
NM_145261.4(DNAJC19):c.210-14_210-13del rs757422860
NM_145261.4(DNAJC19):c.210-291del rs138755965
NM_145261.4(DNAJC19):c.210-4T>C rs2473927709
NM_145261.4(DNAJC19):c.219C>T (p.Ala73=)
NM_145261.4(DNAJC19):c.280+16A>T rs773185733
NM_145261.4(DNAJC19):c.280+19C>A rs1203314065
NM_145261.4(DNAJC19):c.281-15T>G rs3026210
NM_145261.4(DNAJC19):c.281-16_281-15del
NM_145261.4(DNAJC19):c.281-21_281-19del rs1714811182
NM_145261.4(DNAJC19):c.281-21_281-20del rs1465582863
NM_145261.4(DNAJC19):c.281-4A>G rs1256818835
NM_145261.4(DNAJC19):c.281-5T>A rs766954639
NM_145261.4(DNAJC19):c.288T>G (p.Ser96=) rs2108506993
NM_145261.4(DNAJC19):c.28C>T (p.Leu10=)
NM_145261.4(DNAJC19):c.294T>C (p.Tyr98=) rs1341031598
NM_145261.4(DNAJC19):c.3+11C>A
NM_145261.4(DNAJC19):c.3+13T>C rs2108511019
NM_145261.4(DNAJC19):c.3+7G>T
NM_145261.4(DNAJC19):c.30G>C (p.Leu10=)
NM_145261.4(DNAJC19):c.45A>G (p.Ala15=)
NM_145261.4(DNAJC19):c.55+10T>C rs772260835
NM_145261.4(DNAJC19):c.55+20A>T rs1577025780
NM_145261.4(DNAJC19):c.56-17G>C rs2473933857
NM_145261.4(DNAJC19):c.56-7G>T rs2473933827
NM_145261.4(DNAJC19):c.57C>T (p.Gly19=) rs2473933822
NM_145261.4(DNAJC19):c.63C>T (p.Tyr21=) rs145786060

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