ClinVar Miner

List of variants in gene DTNA reported as likely benign for not specified

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Gene type:
ClinVar version:
Total variants: 56
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HGVS dbSNP gnomAD frequency
NM_001386795.1(DTNA):c.1176-8T>C rs41274310 0.00216
NM_001386795.1(DTNA):c.1297C>T (p.His433Tyr) rs139872140 0.00207
NM_001386795.1(DTNA):c.1088T>C (p.Leu363Ser) rs546236565 0.00121
NM_001386795.1(DTNA):c.1000G>A (p.Val334Met) rs148123045 0.00120
NM_001386795.1(DTNA):c.2178A>C (p.Ala726=) rs145486636 0.00063
NM_001386795.1(DTNA):c.1149C>T (p.Tyr383=) rs559493183 0.00051
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.51G>A (p.Gln17=) rs368000651 0.00030
NM_001386795.1(DTNA):c.2108G>A (p.Arg703Gln) rs142009291 0.00028
NM_001386795.1(DTNA):c.-2+6G>T rs560877855 0.00020
NM_001386795.1(DTNA):c.126G>A (p.Arg42=) rs376001633 0.00020
NM_032975.4(DTNA):c.-21G>A rs773687513 0.00019
NM_001386795.1(DTNA):c.1485G>A (p.Ala495=) rs397517443 0.00016
NM_001386795.1(DTNA):c.*2627G>A rs769729466 0.00012
NM_001386795.1(DTNA):c.423A>G (p.Gly141=) rs376651004 0.00006
NM_001386795.1(DTNA):c.603+15T>C rs367772080 0.00006
NM_001386795.1(DTNA):c.*2646T>C rs544029767 0.00005
NM_001386795.1(DTNA):c.1848G>A (p.Thr616=) rs373742103 0.00005
NM_001386795.1(DTNA):c.1431G>A (p.Ser477=) rs202088347 0.00004
NM_001386795.1(DTNA):c.2157C>T (p.Gly719=) rs754959223 0.00004
NM_001386795.1(DTNA):c.877-8C>G rs764675965 0.00004
NM_001386795.1(DTNA):c.149-15C>G rs752608761 0.00003
NM_001386795.1(DTNA):c.1838C>T (p.Pro613Leu) rs145425478 0.00003
NM_001386795.1(DTNA):c.1776C>T (p.Pro592=) rs113072494 0.00002
NM_001386795.1(DTNA):c.2094G>A (p.Ala698=) rs369914309 0.00002
NM_001386795.1(DTNA):c.1435-11A>G rs758607581 0.00001
NM_001386795.1(DTNA):c.1491G>A (p.Lys497=) rs397517444 0.00001
NM_001386795.1(DTNA):c.1758C>T (p.Gly586=) rs1057521757 0.00001
NM_001386795.1(DTNA):c.228C>T (p.Leu76=) rs1002773493 0.00001
NM_001386795.1(DTNA):c.2295+15G>A rs756945985 0.00001
NM_001386795.1(DTNA):c.476G>A (p.Ser159Asn) rs147115867 0.00001
NM_001386795.1(DTNA):c.615G>A (p.Thr205=) rs552069190 0.00001
NM_001386795.1(DTNA):c.67+12T>A rs876657460 0.00001
NM_001386795.1(DTNA):c.708T>C (p.Asn236=) rs1432704587 0.00001
NM_001386795.1(DTNA):c.876+16G>A rs913518501 0.00001
NM_001386795.1(DTNA):c.1254-12G>T rs1057523769
NM_001386795.1(DTNA):c.148+7A>G rs397517445
NM_001386795.1(DTNA):c.1646+18T>C
NM_001386795.1(DTNA):c.1743+2093G>A rs1057522777
NM_001386795.1(DTNA):c.1744-10G>A rs192561043
NM_001386795.1(DTNA):c.1744-10G>T rs192561043
NM_001386795.1(DTNA):c.1764C>T (p.Pro588=) rs151158035
NM_001386795.1(DTNA):c.1766G>A (p.Arg589His) rs200246467
NM_001386795.1(DTNA):c.1770C>A (p.Ser590=) rs570093404
NM_001386795.1(DTNA):c.1821G>T (p.Ala607=) rs9959365
NM_001386795.1(DTNA):c.189G>A (p.Arg63=) rs727505106
NM_001386795.1(DTNA):c.1971T>G (p.Ser657=) rs199855849
NM_001386795.1(DTNA):c.2223T>G (p.Ser741=) rs1057524382
NM_001386795.1(DTNA):c.2295+10T>C rs376012937
NM_001386795.1(DTNA):c.448+17del rs754687179
NM_001386795.1(DTNA):c.449-12T>C rs1057523932
NM_001386795.1(DTNA):c.657G>T (p.Pro219=) rs140446215
NM_001386795.1(DTNA):c.828C>T (p.Ala276=) rs756146461
NM_032975.4(DTNA):c.-127+12G>C rs1057521234
NM_032975.4(DTNA):c.-143C>A rs1053107799

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