ClinVar Miner

List of variants in gene ATL1 reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_015915.5(ATL1):c.574-24G>C rs45570436 0.03833
NM_015915.5(ATL1):c.723+273_723+277del rs140762401 0.01622
NM_015915.5(ATL1):c.1120-47A>C rs17122704 0.01252
NM_015915.5(ATL1):c.1567-78A>G rs113367786 0.01153
NM_015915.5(ATL1):c.631-166G>A rs3015448 0.00894
NM_015915.5(ATL1):c.990+281del rs201856408 0.00881
NM_015915.5(ATL1):c.1567-195dup rs34197551 0.00843
NM_015915.5(ATL1):c.990+287T>C rs79819542 0.00769
NM_015915.5(ATL1):c.1551+241A>G rs140173855 0.00675
NM_015915.5(ATL1):c.283-56G>A rs74051570 0.00640
NM_015915.5(ATL1):c.*305T>C rs2291674 0.00541
NM_015915.5(ATL1):c.1200G>A (p.Lys400=) rs144792471 0.00060
NM_015915.5(ATL1):c.631-7T>A rs186528086 0.00056
NM_015915.5(ATL1):c.1152A>G (p.Pro384=) rs377127492 0.00014
NM_015915.5(ATL1):c.1173C>T (p.His391=) rs149340140 0.00013
NM_015915.5(ATL1):c.990+11C>T rs750229341 0.00003
NM_015915.5(ATL1):c.1047+12T>C rs375882898 0.00002
NM_015915.5(ATL1):c.1551+11C>G rs894699234 0.00002
NM_015915.5(ATL1):c.687C>T (p.Ala229=) rs921388034 0.00001
NM_015915.5(ATL1):c.1551+158T>C rs74414971
NM_015915.5(ATL1):c.1566+49_1566+51del rs138611561
NM_015915.5(ATL1):c.1676A>G (p.Ter559=) rs1442353711
NM_015915.5(ATL1):c.780T>C (p.Cys260=) rs1555365177
NM_015915.5(ATL1):c.991-3dup rs753642042

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