ClinVar Miner

List of variants in gene DNAJC17 reported as likely benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 94
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HGVS dbSNP gnomAD frequency
NM_018163.3(DNAJC17):c.832A>G (p.Met278Val) rs140603715 0.00196
NM_018163.3(DNAJC17):c.495T>C (p.Thr165=) rs200309772 0.00069
NM_018163.3(DNAJC17):c.669C>T (p.Thr223=) rs148868042 0.00052
NM_018163.3(DNAJC17):c.79-14T>C rs368334110 0.00034
NM_018163.3(DNAJC17):c.148+10T>G rs371603327 0.00019
NM_018163.3(DNAJC17):c.648T>C (p.Thr216=) rs200233100 0.00006
NM_018163.3(DNAJC17):c.148+20G>A rs558094855 0.00004
NM_018163.3(DNAJC17):c.264A>G (p.Lys88=) rs754531539 0.00002
NM_018163.3(DNAJC17):c.382-14C>T rs772534444 0.00002
NM_018163.3(DNAJC17):c.148+7C>G rs769104309 0.00001
NM_018163.3(DNAJC17):c.149-7T>C rs577988008 0.00001
NM_018163.3(DNAJC17):c.207+9A>G rs761078607 0.00001
NM_018163.3(DNAJC17):c.382-12C>A rs779170943 0.00001
NM_018163.3(DNAJC17):c.459G>A (p.Glu153=) rs960951302 0.00001
NM_018163.3(DNAJC17):c.588G>A (p.Arg196=) rs759823143 0.00001
NM_018163.3(DNAJC17):c.807A>C (p.Ser269=) rs917427281 0.00001
NM_018163.3(DNAJC17):c.108C>G (p.Leu36=) rs1435768839
NM_018163.3(DNAJC17):c.120A>T (p.Pro40=)
NM_018163.3(DNAJC17):c.148+12dup
NM_018163.3(DNAJC17):c.149-11C>T
NM_018163.3(DNAJC17):c.149-14A>T
NM_018163.3(DNAJC17):c.149-15G>T
NM_018163.3(DNAJC17):c.149-6G>A rs777643471
NM_018163.3(DNAJC17):c.149-9del
NM_018163.3(DNAJC17):c.183G>A (p.Glu61=)
NM_018163.3(DNAJC17):c.189G>A (p.Leu63=)
NM_018163.3(DNAJC17):c.192C>G (p.Thr64=)
NM_018163.3(DNAJC17):c.192C>T (p.Thr64=)
NM_018163.3(DNAJC17):c.193G>A (p.Asp65Asn)
NM_018163.3(DNAJC17):c.207+15dup
NM_018163.3(DNAJC17):c.208-17C>G
NM_018163.3(DNAJC17):c.219C>T (p.Asp73=)
NM_018163.3(DNAJC17):c.248C>T (p.Ala83Val)
NM_018163.3(DNAJC17):c.261G>A (p.Gln87=)
NM_018163.3(DNAJC17):c.295+10A>T
NM_018163.3(DNAJC17):c.295+14T>C
NM_018163.3(DNAJC17):c.296-19A>G
NM_018163.3(DNAJC17):c.296-7T>C
NM_018163.3(DNAJC17):c.312G>A (p.Glu104=)
NM_018163.3(DNAJC17):c.351G>A (p.Glu117=)
NM_018163.3(DNAJC17):c.357G>A (p.Arg119=)
NM_018163.3(DNAJC17):c.375G>A (p.Glu125=)
NM_018163.3(DNAJC17):c.381+20G>A
NM_018163.3(DNAJC17):c.382-11C>G
NM_018163.3(DNAJC17):c.382-18_382-17del
NM_018163.3(DNAJC17):c.384C>T (p.Ile128=)
NM_018163.3(DNAJC17):c.405T>A (p.Gly135=)
NM_018163.3(DNAJC17):c.415C>T (p.Leu139=)
NM_018163.3(DNAJC17):c.420G>A (p.Glu140=) rs2141949359
NM_018163.3(DNAJC17):c.478+18C>T
NM_018163.3(DNAJC17):c.478+19G>A
NM_018163.3(DNAJC17):c.479-19_479-17del
NM_018163.3(DNAJC17):c.479-6T>G
NM_018163.3(DNAJC17):c.517C>T (p.Leu173=)
NM_018163.3(DNAJC17):c.552G>A (p.Glu184=)
NM_018163.3(DNAJC17):c.600+16G>A
NM_018163.3(DNAJC17):c.600+19C>T
NM_018163.3(DNAJC17):c.601-15C>G
NM_018163.3(DNAJC17):c.601-16C>G
NM_018163.3(DNAJC17):c.601-17C>T
NM_018163.3(DNAJC17):c.618C>T (p.Asn206=)
NM_018163.3(DNAJC17):c.681+16G>A
NM_018163.3(DNAJC17):c.681+17del
NM_018163.3(DNAJC17):c.681+7G>T
NM_018163.3(DNAJC17):c.682-18A>T
NM_018163.3(DNAJC17):c.684G>A (p.Glu228=)
NM_018163.3(DNAJC17):c.714G>A (p.Val238=)
NM_018163.3(DNAJC17):c.747A>G (p.Gly249=)
NM_018163.3(DNAJC17):c.771C>T (p.Arg257=) rs748892758
NM_018163.3(DNAJC17):c.79-7C>G
NM_018163.3(DNAJC17):c.792+11A>G
NM_018163.3(DNAJC17):c.792+14C>T
NM_018163.3(DNAJC17):c.792+18G>A
NM_018163.3(DNAJC17):c.792+18G>T rs376380319
NM_018163.3(DNAJC17):c.793-10T>C
NM_018163.3(DNAJC17):c.793-16C>T
NM_018163.3(DNAJC17):c.793-16_793-6del
NM_018163.3(DNAJC17):c.793-30_793-14del
NM_018163.3(DNAJC17):c.793-5G>A
NM_018163.3(DNAJC17):c.793-6C>G
NM_018163.3(DNAJC17):c.804G>A (p.Leu268=)
NM_018163.3(DNAJC17):c.81A>G (p.Val27=)
NM_018163.3(DNAJC17):c.825C>T (p.Ser275=)
NM_018163.3(DNAJC17):c.846C>T (p.Arg282=)
NM_018163.3(DNAJC17):c.852G>A (p.Ala284=)
NM_018163.3(DNAJC17):c.855C>A (p.Ala285=)
NM_018163.3(DNAJC17):c.855C>G (p.Ala285=)
NM_018163.3(DNAJC17):c.870G>T (p.Leu290=)
NM_018163.3(DNAJC17):c.873C>T (p.Ile291=)
NM_018163.3(DNAJC17):c.897G>A (p.Gln299=)
NM_018163.3(DNAJC17):c.909T>C (p.Pro303=)
NM_018163.3(DNAJC17):c.90G>A (p.Ala30=)
NM_018163.3(DNAJC17):c.90G>C (p.Ala30=) rs374405438
NM_018163.3(DNAJC17):c.912G>A (p.Thr304=)

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