ClinVar Miner

List of variants in gene DTNA reported as uncertain significance for not provided

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Gene type:
ClinVar version:
Total variants: 55
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HGVS dbSNP gnomAD frequency
NM_001386795.1(DTNA):c.1297C>T (p.His433Tyr) rs139872140 0.00207
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.1480G>A (p.Asp494Asn) rs144880521 0.00037
NM_001386795.1(DTNA):c.2039G>A (p.Arg680Gln) rs138143719 0.00034
NM_001386795.1(DTNA):c.2108G>A (p.Arg703Gln) rs142009291 0.00028
NM_001386795.1(DTNA):c.1330C>T (p.Arg444Trp) rs199867593 0.00024
NM_001386795.1(DTNA):c.1652G>A (p.Arg551His) rs142108185 0.00011
NM_001386795.1(DTNA):c.614C>T (p.Thr205Met) rs201071018 0.00010
NM_001386795.1(DTNA):c.371A>G (p.His124Arg) rs150147476 0.00009
NM_001386795.1(DTNA):c.229A>G (p.Asn77Asp) rs147782267 0.00007
NM_001386795.1(DTNA):c.239G>A (p.Arg80His) rs774912781 0.00006
NM_001386795.1(DTNA):c.1813C>T (p.Arg605Trp) rs749405895 0.00005
NM_001386795.1(DTNA):c.2153G>A (p.Arg718His) rs111587625 0.00004
NM_001386795.1(DTNA):c.2168C>T (p.Thr723Met) rs200977103 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.1965G>A (p.Met655Ile) rs749109824 0.00003
NM_001386795.1(DTNA):c.479G>A (p.Gly160Glu) rs201550119 0.00003
NM_001386795.1(DTNA):c.604-13T>G rs761037945 0.00003
NM_001386795.1(DTNA):c.937C>T (p.Arg313Cys) rs536920784 0.00003
NM_001386795.1(DTNA):c.182C>G (p.Ala61Gly) rs767620520 0.00002
NM_001386795.1(DTNA):c.2227C>T (p.Arg743Trp) rs774768713 0.00002
NM_001386795.1(DTNA):c.642G>A (p.Met214Ile) rs745752400 0.00002
NM_001386795.1(DTNA):c.869C>T (p.Thr290Met) rs747834756 0.00002
NM_001386795.1(DTNA):c.1007C>T (p.Pro336Leu) rs1293106380 0.00001
NM_001386795.1(DTNA):c.1030G>A (p.Asp344Asn) rs374347283 0.00001
NM_001386795.1(DTNA):c.112G>A (p.Ala38Thr) rs200256996 0.00001
NM_001386795.1(DTNA):c.1613A>G (p.Asn538Ser) rs770486884 0.00001
NM_001386795.1(DTNA):c.1649A>G (p.Gln550Arg) rs1436377008 0.00001
NM_001386795.1(DTNA):c.1695C>T (p.Ser565=) rs774966330 0.00001
NM_001386795.1(DTNA):c.2101C>T (p.His701Tyr) rs772866088 0.00001
NM_001386795.1(DTNA):c.2195C>T (p.Pro732Leu) rs1456993704 0.00001
NM_001386795.1(DTNA):c.2224G>T (p.Val742Phe) rs533568822 0.00001
NM_001386795.1(DTNA):c.2228G>A (p.Arg743Gln) rs371303988 0.00001
NM_001386795.1(DTNA):c.295A>G (p.Thr99Ala) rs200736432 0.00001
NM_001386795.1(DTNA):c.358G>C (p.Asp120His) rs1401291574 0.00001
NM_001386795.1(DTNA):c.476G>A (p.Ser159Asn) rs147115867 0.00001
NM_001386795.1(DTNA):c.646G>T (p.Asp216Tyr) rs769662524 0.00001
NM_001386795.1(DTNA):c.660G>T (p.Gln220His) rs1031348434 0.00001
NM_001386795.1(DTNA):c.695C>T (p.Ala232Val) rs771510372 0.00001
NM_001386795.1(DTNA):c.784C>T (p.His262Tyr) rs369043538 0.00001
NM_001386795.1(DTNA):c.944C>G (p.Pro315Arg) rs138085660 0.00001
NM_001386795.1(DTNA):c.962C>T (p.Pro321Leu) rs774455487 0.00001
GRCh37/hg19 18q12.1(chr18:32019324-32389224)x3
NM_001386795.1(DTNA):c.*2601del rs1198295453
NM_001386795.1(DTNA):c.1295A>C (p.Glu432Ala)
NM_001386795.1(DTNA):c.1325T>C (p.Met442Thr) rs1057524416
NM_001386795.1(DTNA):c.1766G>A (p.Arg589His) rs200246467
NM_001386795.1(DTNA):c.1877G>A (p.Gly626Glu) rs200805008
NM_001386795.1(DTNA):c.1999G>A (p.Gly667Arg)
NM_001386795.1(DTNA):c.209T>C (p.Leu70Pro) rs1060503523
NM_001386795.1(DTNA):c.331C>T (p.Leu111Phe) rs1555801105
NM_001386795.1(DTNA):c.496C>T (p.Arg166Ter) rs2095495862
NM_001386795.1(DTNA):c.574C>T (p.Gln192Ter) rs2149332392

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