ClinVar Miner

List of variants in gene DTNA reported by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Gene type:
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Total variants: 41
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HGVS dbSNP gnomAD frequency
NM_001386795.1(DTNA):c.1903+8G>A rs111817603 0.01438
NM_001386795.1(DTNA):c.933C>T (p.Ser311=) rs114170541 0.00902
NM_001386795.1(DTNA):c.2162+14G>A rs76713874 0.00820
NM_001386795.1(DTNA):c.210G>A (p.Leu70=) rs117571555 0.00459
NM_001386795.1(DTNA):c.1993+7T>C rs138590000 0.00403
NM_001386795.1(DTNA):c.1435-19T>C rs141620769 0.00328
NM_001386795.1(DTNA):c.243A>G (p.Leu81=) rs146923532 0.00285
NM_001386795.1(DTNA):c.999C>T (p.Ile333=) rs61737438 0.00258
NM_001386795.1(DTNA):c.1297C>T (p.His433Tyr) rs139872140 0.00207
NM_001386795.1(DTNA):c.604-14G>T rs397517447 0.00123
NM_001386795.1(DTNA):c.1000G>A (p.Val334Met) rs148123045 0.00120
NM_001386795.1(DTNA):c.955A>G (p.Met319Val) rs141981161 0.00047
NM_001386795.1(DTNA):c.2039G>A (p.Arg680Gln) rs138143719 0.00034
NM_001386795.1(DTNA):c.1485G>A (p.Ala495=) rs397517443 0.00016
NM_001386795.1(DTNA):c.1454G>C (p.Ser485Thr) rs190619495 0.00008
NM_001386795.1(DTNA):c.1915A>G (p.Asn639Asp) rs779045040 0.00006
NM_001386795.1(DTNA):c.603+15T>C rs367772080 0.00006
NM_001386795.1(DTNA):c.1813C>T (p.Arg605Trp) rs749405895 0.00005
NM_001386795.1(DTNA):c.1848G>A (p.Thr616=) rs373742103 0.00005
NM_001386795.1(DTNA):c.675G>A (p.Leu225=) rs376519672 0.00005
NM_001386795.1(DTNA):c.1841C>T (p.Thr614Met) rs757959636 0.00004
NM_001386795.1(DTNA):c.1875G>A (p.Gly625=) rs542483546 0.00004
NM_001386795.1(DTNA):c.904G>A (p.Ala302Thr) rs199983981 0.00004
NM_001386795.1(DTNA):c.1838C>T (p.Pro613Leu) rs145425478 0.00003
NM_001386795.1(DTNA):c.68-7G>A rs372126412 0.00003
NM_001386795.1(DTNA):c.1776C>T (p.Pro592=) rs113072494 0.00002
NM_001386795.1(DTNA):c.1753G>A (p.Ala585Thr) rs767501382 0.00001
NM_001386795.1(DTNA):c.476G>A (p.Ser159Asn) rs147115867 0.00001
NM_001386795.1(DTNA):c.68-5A>G rs1243110074 0.00001
NM_001386795.1(DTNA):c.148+8T>C
NM_001386795.1(DTNA):c.1532+18T>C rs115712655
NM_001386795.1(DTNA):c.1561C>T (p.Arg521Trp)
NM_001386795.1(DTNA):c.1646+17A>G
NM_001386795.1(DTNA):c.1646+18T>C
NM_001386795.1(DTNA):c.1744-10G>T rs192561043
NM_001386795.1(DTNA):c.1766G>A (p.Arg589His) rs200246467
NM_001386795.1(DTNA):c.1821G>T (p.Ala607=) rs9959365
NM_001386795.1(DTNA):c.2083G>T (p.Ala695Ser)
NM_001386795.1(DTNA):c.2295+5A>G rs191417978
NM_001386795.1(DTNA):c.231C>T (p.Asn77=) rs147759402
NM_001386795.1(DTNA):c.828C>T (p.Ala276=) rs756146461

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