C3151568[trait identifier] AND "Precision Medicine Center, Zhengzhou U - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1077036	NM_024426.6(WT1):c.1534C>T (p.Gln512Ter)	WT1 (Q116* +14 more)	Single nucleotide variant (nonsense +1 more)	Nephrotic syndrome, type 4	GPathogenic
Select item 2681780	NM_024426.6(WT1):c.1504G>C (p.Asp502His)	WT1 (D106H +14 more)	Single nucleotide variant (missense variant +1 more)	Nephrotic syndrome, type 4	GLikely pathogenic
Select item 3500	NM_024426.6(WT1):c.1447+4C>T	WT1	Single nucleotide variant (intron variant)	Frasier syndrome +6 more	GPathogenic/Likely pathogenic
Select item 3487	NM_024426.6(WT1):c.1399C>T (p.Arg467Trp)	WT1 (R250W +9 more)	Single nucleotide variant (missense variant +1 more)	not provided +9 more	GPathogenic/Likely pathogenic
Select item 2681778	NM_024426.6(WT1):c.1394T>C (p.Phe465Ser)	WT1 (F211S +11 more)	Single nucleotide variant (missense variant +2 more)	Nephrotic syndrome, type 4	GLikely pathogenic
Select item 2681776	NM_024426.6(WT1):c.1384C>T (p.Gln462Ter)	WT1 (Q208* +11 more)	Single nucleotide variant (nonsense +2 more)	Drash syndrome +3 more	GLikely pathogenic
Select item 2681779	NM_024426.6(WT1):c.1367T>G (p.Phe456Cys)	WT1 (F202C +11 more)	Single nucleotide variant (missense variant +2 more)	Nephrotic syndrome, type 4	GLikely pathogenic
Select item 2681777	NM_024426.6(WT1):c.896T>A (p.Leu299Ter)	WT1 (L258* +4 more)	Single nucleotide variant (nonsense +1 more)	Nephrotic syndrome, type 4	GLikely pathogenic
Select item 2182681	NM_024426.6(WT1):c.392C>T (p.Pro131Leu)	LOC107982234, WT1 (P126L +1 more)	Single nucleotide variant (missense variant +1 more)	Nephrotic syndrome, type 4 +4 more	GConflicting classifications of pathogenicity