ZNF713[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2311254	NM_182633.3(ZNF713):c.98C>T (p.Thr33Met)	ZNF713 (T33M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305575	NM_182633.3(ZNF713):c.276A>G (p.Ile92Met)	ZNF713 (I79M +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2285495	NM_182633.3(ZNF713):c.340A>G (p.Thr114Ala)	ZNF713 (T114A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382103	NM_182633.3(ZNF713):c.441G>C (p.Trp147Cys)	ZNF713 (W147C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508411	NM_182633.3(ZNF713):c.563A>C (p.Asn188Thr)	ZNF713 (N188T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303319	NM_182633.3(ZNF713):c.602C>T (p.Pro201Leu)	ZNF713 (P188L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533641	NM_182633.3(ZNF713):c.605C>T (p.Ser202Phe)	ZNF713 (S202F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197932	NM_182633.3(ZNF713):c.619C>G (p.Leu207Val)	ZNF713 (L207V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197933	NM_182633.3(ZNF713):c.857A>G (p.Tyr286Cys)	ZNF713 (Y286C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259331	NM_182633.3(ZNF713):c.945A>G (p.Ile315Met)	ZNF713 (I302M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197934	NM_182633.3(ZNF713):c.952G>A (p.Gly318Arg)	ZNF713 (G318R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259332	NM_182633.3(ZNF713):c.971G>A (p.Arg324His)	ZNF713 (R311H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279663	NM_182633.3(ZNF713):c.997C>G (p.Leu333Val)	ZNF713 (L333V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602911	NM_182633.3(ZNF713):c.1085G>A (p.Arg362Lys)	ZNF713 (R362K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259334	NM_182633.3(ZNF713):c.1177A>G (p.Thr393Ala)	ZNF713 (T393A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259333	NM_182633.3(ZNF713):c.1269G>T (p.Glu423Asp)	ZNF713 (E410D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance