"Revvity Omics, Revvity"[submitter] AND "WT1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3493	NM_024426.6(WT1):c.1447+5G>A	WT1	Single nucleotide variant (intron variant)	11p partial monosomy syndrome +10 more	GPathogenic
Select item 3505	NM_024426.6(WT1):c.1315C>T (p.Arg439Cys)	WT1 (R222C +8 more)	Single nucleotide variant (missense variant +1 more)	not provided	GPathogenic
Select item 646456	NM_024426.6(WT1):c.1123C>T (p.Arg375Cys)	WT1 (R141C +9 more)	Single nucleotide variant (missense variant +2 more)	Drash syndrome +5 more	GUncertain significance
Select item 661942	NM_024426.6(WT1):c.965+1G>A	WT1	Single nucleotide variant (non-coding transcript variant +1 more)	Wilms tumor 1 +4 more	GLikely pathogenic
Select item 476699	NM_024426.6(WT1):c.314C>G (p.Ala105Gly)	LOC107982234, WT1 (A105G)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +8 more	GConflicting classifications of pathogenicity
Select item 476696	NM_024426.6(WT1):c.218A>T (p.Gln73Leu)	LOC107982234, WT1 (Q73L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +10 more	GUncertain significance

ClinVar