List of variants in gene DES reported as 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: 38

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HGVS	dbSNP	gnomAD frequency
NM_001927.4(DES):c.75A>G (p.Pro25=)	rs1318299	0.89847
NM_001927.4(DES):c.93T>C (p.Ser31=)	rs2017800	0.88201
NM_001927.4(DES):c.579-38C>T	rs12991025	0.50005
NM_001927.3(DES):c.*762T>C	rs11685408	0.49560
NM_001927.4(DES):c.1014G>C (p.Leu338=)	rs12920	0.37027
NM_001927.4(DES):c.828C>T (p.Asp276=)	rs1058261	0.36815
NM_001927.4(DES):c.1104G>A (p.Ala368=)	rs1058284	0.36806
NM_001927.4(DES):c.1244+264G>A	rs2854895	0.35067
NM_001927.4(DES):c.578+11G>A	rs111548596	0.06130
NM_001927.4(DES):c.1289-264C>T	rs58898098	0.03186
NM_001927.4(DES):c.1244+192C>T	rs145871254	0.02924
NM_001927.4(DES):c.669T>C (p.Ile223=)	rs75882680	0.02876
NM_001927.4(DES):c.*468G>T	rs73085265	0.02797
NM_001927.4(DES):c.408C>T (p.Leu136=)	rs111828114	0.02697
NM_001927.4(DES):c.1245-306G>T	rs144177848	0.02423
NM_001927.4(DES):c.1245-201A>G	rs149725578	0.02303
NM_001927.4(DES):c.1245-245T>C	rs146094800	0.02291
NM_001927.4(DES):c.1026C>T (p.Asn342=)	rs61731508	0.02125
NM_001927.4(DES):c.372G>A (p.Glu124=)	rs34365369	0.01950
NM_001927.4(DES):c.638C>T (p.Ala213Val)	rs41272699	0.01015
NM_001927.4(DES):c.1375G>A (p.Val459Ile)	rs73991549	0.00981
NM_001927.4(DES):c.735+20C>T	rs151226355	0.00694
NM_001927.4(DES):c.324G>A (p.Glu108=)	rs138677215	0.00189
NM_001927.4(DES):c.792C>T (p.Asp264=)	rs150370918	0.00168
NM_001927.4(DES):c.18G>A (p.Ser6=)	rs199972656	0.00104
NM_001927.4(DES):c.640-16G>A	rs181712657	0.00028
NM_001927.4(DES):c.897+16C>T	rs370385097	0.00011
NM_001927.4(DES):c.642C>T (p.Asp214=)	rs370239228	0.00009
NM_001927.4(DES):c.699C>T (p.Asn233=)	rs758066814	0.00009
NM_001927.4(DES):c.99C>T (p.Pro33=)	rs774006810	0.00006
NM_001927.4(DES):c.*40del	rs1954530107
NM_001927.4(DES):c.114G>A (p.Ala38=)	rs368901105
NM_001927.4(DES):c.1244+123del	rs374091713
NM_001927.4(DES):c.1353C>T (p.Ile451=)	rs121913002
NM_001927.4(DES):c.423C>T (p.Asn141=)	rs1954375978
NM_001927.4(DES):c.578+64T>G	rs907677
NM_001927.4(DES):c.579-100G>C	rs2666106
NM_001927.4(DES):c.897+4_897+5del	rs397516699

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