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 0.00190
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.193G>A (p.Asp65Asn) rs181009746 0.00014
NM_018163.3(DNAJC17):c.248C>T (p.Ala83Val) rs145641293 0.00012
NM_018163.3(DNAJC17):c.897G>A (p.Gln299=) rs201018452 0.00007
NM_018163.3(DNAJC17):c.90G>A (p.Ala30=) rs374405438 0.00007
NM_018163.3(DNAJC17):c.648T>C (p.Thr216=) rs200233100 0.00006
NM_018163.3(DNAJC17):c.681+7G>T rs919764701 0.00006
NM_018163.3(DNAJC17):c.148+20G>A rs558094855 0.00004
NM_018163.3(DNAJC17):c.684G>A (p.Glu228=) rs563474521 0.00004
NM_018163.3(DNAJC17):c.120A>T (p.Pro40=) rs1360556449 0.00003
NM_018163.3(DNAJC17):c.478+19G>A rs369765784 0.00003
NM_018163.3(DNAJC17):c.804G>A (p.Leu268=) rs766791560 0.00003
NM_018163.3(DNAJC17):c.264A>G (p.Lys88=) rs754531539 0.00002
NM_018163.3(DNAJC17):c.357G>A (p.Arg119=) rs149784969 0.00002
NM_018163.3(DNAJC17):c.382-14C>T rs772534444 0.00002
NM_018163.3(DNAJC17):c.478+18C>T rs761869231 0.00002
NM_018163.3(DNAJC17):c.149-11C>T rs986744644 0.00001
NM_018163.3(DNAJC17):c.149-14A>T rs745975361 0.00001
NM_018163.3(DNAJC17):c.149-15G>T rs185892927 0.00001
NM_018163.3(DNAJC17):c.149-7T>C rs577988008 0.00001
NM_018163.3(DNAJC17):c.189G>A (p.Leu63=) rs1474263206 0.00001
NM_018163.3(DNAJC17):c.207+9A>G rs761078607 0.00001
NM_018163.3(DNAJC17):c.261G>A (p.Gln87=) rs571440654 0.00001
NM_018163.3(DNAJC17):c.295+14T>C rs1351170839 0.00001
NM_018163.3(DNAJC17):c.296-7T>C rs1471443555 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.600+16G>A rs886555895 0.00001
NM_018163.3(DNAJC17):c.601-17C>T rs767475648 0.00001
NM_018163.3(DNAJC17):c.681+16G>A rs910652077 0.00001
NM_018163.3(DNAJC17):c.682-18A>T rs568722122 0.00001
NM_018163.3(DNAJC17):c.747A>G (p.Gly249=) rs371259333 0.00001
NM_018163.3(DNAJC17):c.792+11A>G rs747494769 0.00001
NM_018163.3(DNAJC17):c.792+14C>T rs758852497 0.00001
NM_018163.3(DNAJC17):c.793-16C>T rs1303749991 0.00001
NM_018163.3(DNAJC17):c.793-5G>A rs368897833 0.00001
NM_018163.3(DNAJC17):c.793-6C>G rs1596069455 0.00001
NM_018163.3(DNAJC17):c.807A>C (p.Ser269=) rs917427281 0.00001
NM_018163.3(DNAJC17):c.912G>A (p.Thr304=) rs760787274 0.00001
NM_018163.3(DNAJC17):c.108C>G (p.Leu36=) rs1435768839
NM_018163.3(DNAJC17):c.148+12dup rs2504667987
NM_018163.3(DNAJC17):c.148+7C>G rs769104309
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=) rs1889423273
NM_018163.3(DNAJC17):c.192C>G (p.Thr64=)
NM_018163.3(DNAJC17):c.192C>T (p.Thr64=) rs377573607
NM_018163.3(DNAJC17):c.207+15dup rs1026529497
NM_018163.3(DNAJC17):c.208-17C>G
NM_018163.3(DNAJC17):c.219C>T (p.Asp73=) rs1889413597
NM_018163.3(DNAJC17):c.295+10A>T rs2504666290
NM_018163.3(DNAJC17):c.296-19A>G rs1443783754
NM_018163.3(DNAJC17):c.312G>A (p.Glu104=) rs979435654
NM_018163.3(DNAJC17):c.351G>A (p.Glu117=) rs1269936794
NM_018163.3(DNAJC17):c.375G>A (p.Glu125=) rs2504662787
NM_018163.3(DNAJC17):c.381+20G>A
NM_018163.3(DNAJC17):c.382-11C>G rs771415170
NM_018163.3(DNAJC17):c.382-18_382-17del rs1889319236
NM_018163.3(DNAJC17):c.384C>T (p.Ile128=) rs146094788
NM_018163.3(DNAJC17):c.405T>A (p.Gly135=) rs1383736592
NM_018163.3(DNAJC17):c.415C>T (p.Leu139=) rs1889317159
NM_018163.3(DNAJC17):c.420G>A (p.Glu140=) rs2141949359
NM_018163.3(DNAJC17):c.479-19_479-17del rs2504661016
NM_018163.3(DNAJC17):c.479-6T>G
NM_018163.3(DNAJC17):c.517C>T (p.Leu173=) rs2504660904
NM_018163.3(DNAJC17):c.552G>A (p.Glu184=) rs2504659893
NM_018163.3(DNAJC17):c.600+19C>T rs2504659735
NM_018163.3(DNAJC17):c.601-15C>G
NM_018163.3(DNAJC17):c.601-16C>G rs1352187875
NM_018163.3(DNAJC17):c.618C>T (p.Asn206=) rs1047029408
NM_018163.3(DNAJC17):c.681+17del
NM_018163.3(DNAJC17):c.714G>A (p.Val238=)
NM_018163.3(DNAJC17):c.771C>T (p.Arg257=) rs748892758
NM_018163.3(DNAJC17):c.79-7C>G
NM_018163.3(DNAJC17):c.792+18G>A rs376380319
NM_018163.3(DNAJC17):c.792+18G>T rs376380319
NM_018163.3(DNAJC17):c.793-10T>C rs2504646255
NM_018163.3(DNAJC17):c.793-16_793-6del rs766720155
NM_018163.3(DNAJC17):c.793-30_793-14del rs752093384
NM_018163.3(DNAJC17):c.81A>G (p.Val27=) rs758592285
NM_018163.3(DNAJC17):c.825C>T (p.Ser275=) rs773754995
NM_018163.3(DNAJC17):c.846C>T (p.Arg282=)
NM_018163.3(DNAJC17):c.852G>A (p.Ala284=) rs151327520
NM_018163.3(DNAJC17):c.855C>A (p.Ala285=) rs747324198
NM_018163.3(DNAJC17):c.855C>G (p.Ala285=) rs747324198
NM_018163.3(DNAJC17):c.870G>T (p.Leu290=) rs2504645914
NM_018163.3(DNAJC17):c.873C>T (p.Ile291=)
NM_018163.3(DNAJC17):c.909T>C (p.Pro303=) rs1888993702
NM_018163.3(DNAJC17):c.90G>C (p.Ala30=) rs374405438

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