ClinVar Miner

List of variants in gene DTNA reported as benign by Invitae

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Gene type:
ClinVar version:
Total variants: 28
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HGVS dbSNP gnomAD frequency
NM_001386795.1(DTNA):c.1743+14G>A rs1617318 0.37431
NM_001386795.1(DTNA):c.1903+17T>C rs541157 0.16470
NM_001386795.1(DTNA):c.1903+8G>A rs111817603 0.01438
NM_001386795.1(DTNA):c.1821G>A (p.Ala607=) rs9959365 0.00984
NM_001386795.1(DTNA):c.537G>T (p.Thr179=) rs11877640 0.00956
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.1438C>A (p.Pro480Thr) rs77320474 0.00593
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.1176-8T>C rs41274310 0.00216
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.2178A>C (p.Ala726=) rs145486636 0.00063
NM_001386795.1(DTNA):c.92G>A (p.Arg31Gln) rs202046233 0.00063
NM_001386795.1(DTNA):c.1002-2330A>G rs369005625 0.00008
NM_001386795.1(DTNA):c.1454G>C (p.Ser485Thr) rs190619495 0.00008
NM_001386795.1(DTNA):c.1875G>A (p.Gly625=) rs542483546 0.00004
NM_001386795.1(DTNA):c.2295+15G>A rs756945985 0.00001
NM_001386795.1(DTNA):c.93A>G (p.Arg31=) rs778817036 0.00001
NM_001386795.1(DTNA):c.1532+18T>C rs115712655
NM_001386795.1(DTNA):c.1744-10G>A rs192561043
NM_001386795.1(DTNA):c.1744-10G>T rs192561043
NM_001386795.1(DTNA):c.231C>T (p.Asn77=) rs147759402
NM_001386795.1(DTNA):c.710-5dup

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