C4551772[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1031002	NM_032856.5(WDR73):c.1132C>T (p.Arg378Cys)	WDR73 (R378C)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 1012861	NM_032856.5(WDR73):c.1130C>T (p.Pro377Leu)	WDR73 (P377L)	Single nucleotide variant (missense variant +1 more)	Galloway-Mowat syndrome 1 +1 more	GUncertain significance
Select item 1219713	NM_032856.5(WDR73):c.926ATGGAACACGGAGCCAAG[3] (p.309DGTRSQ[3])	WDR73	Microsatellite (inframe_insertion +1 more)	not provided +1 more	GUncertain significance
Select item 598566	NM_032856.5(WDR73):c.952C>T (p.Arg318Trp)	WDR73 (R318W)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +2 more	GUncertain significance
Select item 784686	NM_032856.5(WDR73):c.883+8C>T	WDR73	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 1551791	NM_032856.5(WDR73):c.816T>C (p.Pro272=)	WDR73	Single nucleotide variant (synonymous variant +1 more)	Galloway-Mowat syndrome 1 +1 more	GLikely benign
Select item 450013	NM_032856.5(WDR73):c.766C>T (p.Arg256Trp)	WDR73 (R256W)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 1311557	NM_032856.5(WDR73):c.596G>A (p.Arg199Gln)	WDR73 (R199Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +2 more	GUncertain significance
Select item 429429	NM_032856.5(WDR73):c.518-10G>A	WDR73	Single nucleotide variant (intron variant)	Galloway-Mowat syndrome 1 +1 more	GConflicting classifications of pathogenicity
Select item 1194019	NM_032856.5(WDR73):c.354T>G (p.Asp118Glu)	WDR73 (D118E)	Single nucleotide variant (missense variant +1 more)	Galloway-Mowat syndrome 1 +1 more	GConflicting classifications of pathogenicity
Select item 770626	NM_032856.5(WDR73):c.336G>A (p.Gln112=)	WDR73	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 728212	NM_032856.5(WDR73):c.267A>G (p.Leu89=)	WDR73	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 1215509	NM_032856.5(WDR73):c.41+262G>A	WDR73	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +1 more	GLikely benign
Select item 738079	NM_032856.5(WDR73):c.33C>T (p.Ser11=)	WDR73	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign