C1856113[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 935467	NM_014795.4(ZEB2):c.3527C>A (p.Pro1176His)	ZEB2 (P1152H +1 more)	Single nucleotide variant (missense variant)	Mowat-Wilson syndrome	GUncertain significance
Select item 95632	NM_014795.4(ZEB2):c.2887-4G>A	ZEB2	Single nucleotide variant (intron variant)	Inborn genetic diseases +2 more	GBenign
Select item 450276	NM_014795.4(ZEB2):c.2471T>C (p.Met824Thr)	ZEB2 (M824T +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 378869	NM_014795.4(ZEB2):c.2256G>A (p.Thr752=)	ZEB2	Single nucleotide variant (synonymous variant)	not specified +3 more	GLikely benign
Select item 95631	NM_014795.4(ZEB2):c.2255C>T (p.Thr752Met)	ZEB2 (T752M +1 more)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign/Likely benign
Select item 95627	NM_014795.4(ZEB2):c.2141C>T (p.Pro714Leu)	ZEB2 (P714L +1 more)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign/Likely benign
Select item 181737	NM_014795.4(ZEB2):c.2084G>A (p.Arg695Gln)	ZEB2 (R695Q +1 more)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 4755	NM_014795.4(ZEB2):c.2083C>T (p.Arg695Ter)	ZEB2 (R695* +1 more)	Single nucleotide variant (nonsense)	not provided +1 more	GPathogenic
Select item 181736	NM_014795.4(ZEB2):c.1876G>A (p.Gly626Arg)	ZEB2 (G626R +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 137947	NM_014795.4(ZEB2):c.1840C>T (p.Leu614=)	ZEB2	Single nucleotide variant (synonymous variant)	Mowat-Wilson syndrome +2 more	GBenign/Likely benign
Select item 95622	NM_014795.4(ZEB2):c.1480C>T (p.Pro494Ser)	ZEB2 (P494S +1 more)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign/Likely benign
Select item 181731	NM_014795.4(ZEB2):c.1283T>C (p.Val428Ala)	ZEB2 (V428A +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 95618	NM_014795.4(ZEB2):c.1161A>G (p.Leu387=)	ZEB2	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 546312	NM_014795.4(ZEB2):c.807+3G>T	ZEB2	Single nucleotide variant (intron variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 466290	NM_014795.4(ZEB2):c.593-9C>T	ZEB2	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign