List of variants in gene DES reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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: 46

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HGVS	dbSNP	gnomAD frequency
NM_001927.4(DES):c.166G>C (p.Val56Leu)	rs578066781	0.00021
NM_001927.4(DES):c.643G>A (p.Val215Met)	rs144908941	0.00016
NM_001927.4(DES):c.407T>A (p.Leu136His)	rs397516695	0.00011
NM_001927.4(DES):c.216C>A (p.Ser72Arg)	rs375719734	0.00008
NM_001927.4(DES):c.193G>A (p.Gly65Ser)	rs397516692	0.00007
NM_001927.4(DES):c.*695C>T	rs1452548510	0.00006
NM_001927.4(DES):c.1009G>A (p.Ala337Thr)	rs59962885	0.00005
NM_001927.4(DES):c.1123C>T (p.Arg375Trp)	rs375218723	0.00005
NM_001927.4(DES):c.109C>T (p.Arg37Trp)	rs537881554	0.00004
NM_001927.4(DES):c.1243C>T (p.Arg415Trp)	rs751942358	0.00004
NM_001927.4(DES):c.662C>T (p.Ala221Val)	rs746814065	0.00004
NM_001927.4(DES):c.1064G>A (p.Arg355Gln)	rs61368398	0.00003
NM_001927.4(DES):c.229A>G (p.Thr77Ala)	rs769034192	0.00003
NM_001927.4(DES):c.233G>T (p.Arg78Leu)	rs573916832	0.00003
NM_001927.4(DES):c.391C>A (p.Gln131Lys)	rs771499260	0.00003
NM_001927.4(DES):c.1049G>A (p.Arg350Gln)	rs57965306	0.00002
NM_001927.4(DES):c.1325C>A (p.Thr442Asn)	rs121913005	0.00002
NM_001927.4(DES):c.167T>A (p.Val56Glu)	rs1170549656	0.00002
NM_001927.4(DES):c.680G>A (p.Arg227His)	rs141486420	0.00002
NM_001927.4(DES):c.728A>G (p.His243Arg)	rs1410266369	0.00002
NM_001927.4(DES):c.1027G>A (p.Asp343Asn)	rs763903197	0.00001
NM_001927.4(DES):c.1038G>A (p.Met346Ile)	rs778340812	0.00001
NM_001927.4(DES):c.1079C>T (p.Ala360Val)	rs141592925	0.00001
NM_001927.4(DES):c.1105C>T (p.Arg369Cys)	rs1475674849	0.00001
NM_001927.4(DES):c.1148G>A (p.Arg383His)	rs1292042317	0.00001
NM_001927.4(DES):c.1217G>A (p.Arg406Gln)	rs1057520275	0.00001
NM_001927.4(DES):c.1258A>C (p.Ile420Leu)	rs1427557970	0.00001
NM_001927.4(DES):c.1333A>G (p.Thr445Ala)	rs267607498	0.00001
NM_001927.4(DES):c.517C>A (p.Arg173Ser)	rs752944882	0.00001
NM_001927.4(DES):c.615G>C (p.Glu205Asp)	rs1295010624	0.00001
NM_001927.4(DES):c.65C>G (p.Pro22Arg)	rs748158450	0.00001
NM_001927.4(DES):c.727C>T (p.His243Tyr)	rs769647148	0.00001
NM_001927.4(DES):c.817G>A (p.Ala273Thr)	rs770258461	0.00001
NM_001927.4(DES):c.1078G>T (p.Ala360Ser)	rs121913000
NM_001927.4(DES):c.109C>G (p.Arg37Gly)	rs537881554
NM_001927.4(DES):c.1104_1105delinsAT (p.Arg369Cys)	rs2125168717
NM_001927.4(DES):c.1244G>A (p.Arg415Gln)	rs1262288015
NM_001927.4(DES):c.1286G>A (p.Arg429Gln)	rs200580581
NM_001927.4(DES):c.182G>A (p.Gly61Asp)	rs1447436485
NM_001927.4(DES):c.245C>T (p.Ser82Phe)	rs1358038961
NM_001927.4(DES):c.322G>A (p.Glu108Lys)	rs62636490
NM_001927.4(DES):c.404C>G (p.Ala135Gly)	rs546741834
NM_001927.4(DES):c.466G>A (p.Glu156Lys)	rs765471098
NM_001927.4(DES):c.494A>G (p.Gln165Arg)	rs1369044757
NM_001927.4(DES):c.709G>A (p.Ala237Thr)	rs397516697
NM_001927.4(DES):c.93T>G (p.Ser31Arg)	rs2017800

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