List of variants in gene DES reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001927.4(DES):c.170C>T (p.Ser57Leu)	rs372825868	0.00077
NM_001927.4(DES):c.656C>T (p.Thr219Ile)	rs144901249	0.00058
NM_001927.4(DES):c.665G>A (p.Arg222His)	rs367961979	0.00011
NM_001927.4(DES):c.216C>A (p.Ser72Arg)	rs375719734	0.00008
NM_001927.4(DES):c.1158C>T (p.Arg386=)	rs774323736	0.00004
NM_001927.4(DES):c.680G>A (p.Arg227His)	rs141486420	0.00002
NM_001927.4(DES):c.1079C>T (p.Ala360Val)	rs141592925	0.00001
NM_001927.4(DES):c.524G>A (p.Arg175His)	rs878854472	0.00001
NM_001927.4(DES):c.1345_1353del (p.Lys449_Ile451del)	rs1064796352
NM_001927.4(DES):c.404C>T (p.Ala135Val)	rs546741834

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