ClinVar Miner

List of variants in gene ATL1 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 35
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HGVS dbSNP gnomAD frequency
NM_015915.5(ATL1):c.523-112A>G rs2291672 0.80189
NM_015915.5(ATL1):c.351G>A (p.Glu117=) rs1060197 0.79691
NM_015915.5(ATL1):c.574-132G>A rs3015455 0.79481
NM_015915.5(ATL1):c.1552-103_1552-102insTTCTT rs3080579 0.79380
NM_015915.5(ATL1):c.990+245G>A rs963626 0.71630
NM_015915.5(ATL1):c.1048-168G>T rs3736307 0.67040
NM_015915.5(ATL1):c.862+286C>T rs1353204 0.51253
NM_015915.5(ATL1):c.630+105G>A rs10131107 0.49391
NM_015915.5(ATL1):c.862+220C>T rs1389650 0.48730
NM_015915.5(ATL1):c.1119+149T>G rs6572678 0.48687
NM_015915.5(ATL1):c.1119+136_1119+137insAT rs10626021 0.48669
NM_015915.5(ATL1):c.863-54A>G rs11157759 0.45951
NM_015915.5(ATL1):c.522+154G>A rs2934683 0.28655
NM_015915.5(ATL1):c.84A>G (p.Pro28=) rs35014209 0.18809
NM_015915.5(ATL1):c.630+7G>A rs3759588 0.17660
NM_015915.5(ATL1):c.1048-58G>A rs75329155 0.08159
NM_015915.5(ATL1):c.1551+249T>C rs117783723 0.04163
NM_015915.5(ATL1):c.35-74G>C rs77224287 0.03854
NM_015915.5(ATL1):c.418-175T>C rs78241205 0.03841
NM_015915.5(ATL1):c.1552-176C>T rs78649712 0.03090
NM_015915.5(ATL1):c.1119+150A>G rs59955584 0.03068
NM_015915.5(ATL1):c.705C>T (p.Phe235=) rs35044504 0.02457
NM_015915.5(ATL1):c.35-14G>A rs115722924 0.00906
NM_015915.5(ATL1):c.693T>C (p.Gly231=) rs139720661 0.00790
NM_015915.5(ATL1):c.1230G>A (p.Gly410=) rs148548325 0.00531
NM_015915.5(ATL1):c.621G>A (p.Lys207=) rs35629585 0.00263
NM_015915.5(ATL1):c.669C>T (p.Tyr223=) rs146975855 0.00059
NM_015915.5(ATL1):c.306C>A (p.Asp102Glu) rs145204580 0.00010
NM_015915.5(ATL1):c.417+3A>G rs200310890 0.00009
NM_015915.5(ATL1):c.1552-24_1552-20del rs202061961
NM_015915.5(ATL1):c.1552-68_1552-67insATA rs3080581
NM_015915.5(ATL1):c.1567-77C>A rs75154648
NM_015915.5(ATL1):c.418-19G>T rs2934684
NM_015915.5(ATL1):c.574-57TC[11] rs3834518
NM_015915.5(ATL1):c.630+264del rs72247480

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