"KCCC/NGS Laboratory, Kuwait Cancer Control Center"[submitter] AND "WT - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 261709	NM_024426.6(WT1):c.1448-49T>C	WT1	Single nucleotide variant (intron variant)	Wilms tumor 1 +6 more	GBenign
Select item 414077	NM_024426.6(WT1):c.1354+9G>A	WT1	Single nucleotide variant (intron variant)	Wilms tumor 1 +4 more	GLikely benign
Select item 224479	NM_024426.6(WT1):c.1265-32C>A	WT1	Single nucleotide variant (intron variant)	not specified +6 more	GBenign
Select item 198591	NM_024426.6(WT1):c.1122A>G (p.Arg374=)	WT1	Single nucleotide variant (synonymous variant +2 more)	Nephrotic syndrome, type 4 +8 more	GBenign
Select item 261708	NM_024426.6(WT1):c.1074A>G (p.Gln358=)	WT1	Single nucleotide variant (synonymous variant +2 more)	not specified +9 more	GBenign
Select item 261716	NM_024426.6(WT1):c.887+16G>A	WT1	Single nucleotide variant (intron variant)	Wilms tumor 1 +7 more	GBenign
Select item 476710	NM_024426.6(WT1):c.662-5C>T	WT1	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +5 more	GConflicting classifications of pathogenicity
Select item 261713	NM_024426.6(WT1):c.609C>T (p.Asn203=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Wilms tumor 1 +8 more	GBenign
Select item 261712	NM_024426.6(WT1):c.513C>A (p.Gly171=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	not specified +8 more	GBenign/Likely benign
Select item 193454	NM_024426.6(WT1):c.345C>T (p.Pro115=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	not provided +8 more	GBenign
Select item 241480	NM_024426.6(WT1):c.309C>A (p.Gly103=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	Drash syndrome +7 more	GConflicting classifications of pathogenicity
Select item 241479	NM_024426.6(WT1):c.216G>T (p.Gln72His)	LOC107982234, WT1 (Q72H)	Single nucleotide variant (missense variant +1 more)	Drash syndrome +7 more	GBenign/Likely benign
Select item 261710	NM_024426.6(WT1):c.213G>T (p.Pro71=)	LOC107982234, WT1	Single nucleotide variant (synonymous variant +1 more)	not provided +8 more	GBenign