ClinVar Miner

List of variants in gene ATL1 studied for Spastic paraplegia, autosomal dominant

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Total variants: 28
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HGVS dbSNP
NM_015915.4(ATL1):c.*212T>A rs372073012
NM_015915.4(ATL1):c.*304C>T rs886050533
NM_015915.4(ATL1):c.*305T>C rs2291674
NM_015915.4(ATL1):c.*392C>A rs138209522
NM_015915.4(ATL1):c.*450A>G rs183817549
NM_015915.4(ATL1):c.*475G>A rs111734056
NM_015915.4(ATL1):c.*528A>C rs886050534
NM_015915.4(ATL1):c.*621G>A rs1060183
NM_015915.4(ATL1):c.*653T>C rs886050535
NM_015915.4(ATL1):c.1152A>G (p.Pro384=) rs377127492
NM_015915.4(ATL1):c.1173C>T (p.His391=) rs149340140
NM_015915.4(ATL1):c.1567-14T>C rs886050532
NM_015915.4(ATL1):c.1623T>G (p.Ala541=) rs777479928
NM_015915.4(ATL1):c.351G>A (p.Glu117=) rs1060197
NM_015915.4(ATL1):c.408T>C (p.Asp136=) rs76375909
NM_015915.4(ATL1):c.417+3A>G rs200310890
NM_015915.4(ATL1):c.523-13T>C rs778508132
NM_015915.4(ATL1):c.621G>A (p.Lys207=) rs35629585
NM_015915.4(ATL1):c.622C>T (p.Pro208Ser) rs147839037
NM_015915.4(ATL1):c.630+6C>A rs886050531
NM_015915.4(ATL1):c.630+7G>A rs3759588
NM_015915.4(ATL1):c.669C>T (p.Tyr223=) rs146975855
NM_015915.4(ATL1):c.693T>C (p.Gly231=) rs139720661
NM_015915.4(ATL1):c.705C>T (p.Phe235=) rs35044504
NM_015915.4(ATL1):c.756C>T (p.Asn252=) rs771031586
NM_015915.4(ATL1):c.84A>G (p.Pro28=) rs35014209
NM_015915.4(ATL1):c.969G>C (p.Arg323=) rs753145983
NM_015915.4(ATL1):c.991-6T>G rs192428744

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