List of variants in gene DTNA reported as likely benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 83

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HGVS	dbSNP	gnomAD frequency
NM_001386795.1(DTNA):c.2295+321C>T	rs140634474	0.02139
NM_001386795.1(DTNA):c.1532+220G>C	rs112067476	0.01472
NM_032975.4(DTNA):c.-126-85723C>T	rs116012046	0.01138
NM_001386795.1(DTNA):c.-1-279A>G	rs6650657	0.01080
NM_001386795.1(DTNA):c.2296-102C>G	rs28650208	0.01067
NM_001386795.1(DTNA):c.1434+222G>A	rs71363470	0.00966
NM_001386795.1(DTNA):c.449-106A>G	rs7237746	0.00951
NM_001386795.1(DTNA):c.362+260T>C	rs34669760	0.00922
NM_001386795.1(DTNA):c.1175+208T>G	rs77785636	0.00888
NM_001386795.1(DTNA):c.1175+190C>T	rs148773881	0.00886
NM_001386795.1(DTNA):c.1002-2535A>G	rs115311309	0.00885
NM_001386795.1(DTNA):c.*2523A>G	rs114631141	0.00813
NM_001386795.1(DTNA):c.1086-472A>G	rs117594057	0.00794
NM_001386795.1(DTNA):c.1086-516T>A	rs139678659	0.00718
NM_001386795.1(DTNA):c.68-242C>G	rs190610201	0.00703
NM_001386795.1(DTNA):c.1435-83C>A	rs73949013	0.00655
NM_001386795.1(DTNA):c.1646+283G>A	rs185245450	0.00514
NM_001386795.1(DTNA):c.1176-254A>G	rs73418640	0.00462
NM_001386795.1(DTNA):c.1532+135T>C	rs75355506	0.00369
NM_001386795.1(DTNA):c.1743+72G>A	rs116598952	0.00296
NM_001386795.1(DTNA):c.148+29A>G	rs75545220	0.00231
NM_001386795.1(DTNA):c.1904-230T>C	rs147637404	0.00230
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.1149C>T (p.Tyr383=)	rs559493183	0.00051
NM_001386795.1(DTNA):c.1176-47C>A	rs150347998	0.00048
NM_001386795.1(DTNA):c.955A>G (p.Met319Val)	rs141981161	0.00047
NM_001386795.1(DTNA):c.51G>A (p.Gln17=)	rs368000651	0.00030
NM_001386795.1(DTNA):c.1404G>A (p.Ala468=)	rs144776465	0.00025
NM_001386795.1(DTNA):c.-2+6G>T	rs560877855	0.00020
NM_001386795.1(DTNA):c.2283T>C (p.Asp761=)	rs187028045	0.00020
NM_001386795.1(DTNA):c.*2600C>T	rs794729006	0.00019
NM_001386795.1(DTNA):c.1918T>C (p.Leu640=)	rs372620035	0.00019
NM_032975.4(DTNA):c.-21G>A	rs773687513	0.00019
NM_001386795.1(DTNA):c.*2571C>T	rs779508079	0.00016
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.1308C>T (p.Ile436=)	rs368913791	0.00011
NM_001386795.1(DTNA):c.1086-321A>C	rs191973037	0.00010
NM_001386795.1(DTNA):c.*2592C>T	rs530439494	0.00008
NM_001386795.1(DTNA):c.1454G>C (p.Ser485Thr)	rs190619495	0.00008
NM_001386795.1(DTNA):c.1592C>T (p.Thr531Met)	rs199828427	0.00006
NM_001386795.1(DTNA):c.423A>G (p.Gly141=)	rs376651004	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.675G>A (p.Leu225=)	rs376519672	0.00005
NM_001386795.1(DTNA):c.1431G>A (p.Ser477=)	rs202088347	0.00004
NM_001386795.1(DTNA):c.1875G>A (p.Gly625=)	rs542483546	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.2094G>A (p.Ala698=)	rs369914309	0.00002
NM_001386795.1(DTNA):c.1435-11A>G	rs758607581	0.00001
NM_001386795.1(DTNA):c.1758C>T (p.Gly586=)	rs1057521757	0.00001
NM_001386795.1(DTNA):c.2224G>T (p.Val742Phe)	rs533568822	0.00001
NM_001386795.1(DTNA):c.2295+15G>A	rs756945985	0.00001
NM_001386795.1(DTNA):c.615G>A (p.Thr205=)	rs552069190	0.00001
NM_001386795.1(DTNA):c.68-5A>G	rs1243110074	0.00001
NM_001386795.1(DTNA):c.708T>C (p.Asn236=)	rs1432704587	0.00001
NM_001386795.1(DTNA):c.720G>A (p.Pro240=)	rs778548302	0.00001
NM_001386795.1(DTNA):c.840T>C (p.His280=)	rs933476610	0.00001
NM_001386795.1(DTNA):c.876+16G>A	rs913518501	0.00001
NM_001386795.1(DTNA):c.93A>G (p.Arg31=)	rs778817036	0.00001
NM_001386795.1(DTNA):c.1001+125dup
NM_001386795.1(DTNA):c.1002-2520del	rs140760840
NM_001386795.1(DTNA):c.1002-2641_1002-2640dup	rs35456039
NM_001386795.1(DTNA):c.1002-2642_1002-2640del	rs35456039
NM_001386795.1(DTNA):c.1254-12G>T	rs1057523769
NM_001386795.1(DTNA):c.1347-69del	rs150998285
NM_001386795.1(DTNA):c.1545G>A (p.Gln515=)	rs1057521200
NM_001386795.1(DTNA):c.1743+2093G>A	rs1057522777
NM_001386795.1(DTNA):c.1743+212G>A	rs576838640
NM_001386795.1(DTNA):c.1764C>T (p.Pro588=)	rs151158035
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.537G>A (p.Thr179=)	rs11877640
NM_001386795.1(DTNA):c.657G>T (p.Pro219=)	rs140446215
NM_032975.4(DTNA):c.-126-85981G>C
NM_032975.4(DTNA):c.-127+12G>C	rs1057521234
NM_032975.4(DTNA):c.-143C>A	rs1053107799

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