ZNF354A[gene] and "single gene"[properties] - ClinVar

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Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2559862	NM_005649.3(ZNF354A):c.1766A>T (p.His589Leu)	ZNF354A (H547L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459508	NM_005649.3(ZNF354A):c.1744A>G (p.Thr582Ala)	ZNF354A (T582A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613268	NM_005649.3(ZNF354A):c.1730C>T (p.Pro577Leu)	ZNF354A (P577L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2234904	NM_005649.3(ZNF354A):c.1645C>T (p.Pro549Ser)	ZNF354A (P549S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2656128	NM_005649.3(ZNF354A):c.1500G>C (p.Gly500=)	ZNF354A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 768053	NM_005649.3(ZNF354A):c.1437A>C (p.Ser479=)	ZNF354A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3335583	NM_005649.3(ZNF354A):c.1432A>C (p.Ser478Arg)	ZNF354A (S436R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338060	NM_005649.3(ZNF354A):c.1286G>A (p.Arg429Gln)	ZNF354A (R387Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195354	NM_005649.3(ZNF354A):c.1247G>A (p.Gly416Glu)	ZNF354A (G416E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489256	NM_005649.3(ZNF354A):c.1070A>G (p.Asn357Ser)	ZNF354A (N357S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356105	NM_005649.3(ZNF354A):c.1043A>T (p.His348Leu)	ZNF354A (H306L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382083	NM_005649.3(ZNF354A):c.983A>G (p.Tyr328Cys)	ZNF354A (Y328C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2656129	NM_005649.3(ZNF354A):c.933A>C (p.Ser311=)	ZNF354A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3195362	NM_005649.3(ZNF354A):c.755G>A (p.Ser252Asn)	ZNF354A (S252N +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2270250	NM_005649.3(ZNF354A):c.724T>C (p.Phe242Leu)	ZNF354A (F242L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254483	NM_005649.3(ZNF354A):c.688C>T (p.Arg230Cys)	ZNF354A (R188C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195361	NM_005649.3(ZNF354A):c.637C>T (p.Arg213Cys)	ZNF354A (R213C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311136	NM_005649.3(ZNF354A):c.560C>T (p.Pro187Leu)	ZNF354A (P187L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303018	NM_005649.3(ZNF354A):c.533A>G (p.Gln178Arg)	ZNF354A (Q136R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195360	NM_005649.3(ZNF354A):c.520C>T (p.Leu174Phe)	ZNF354A (L132F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354145	NM_005649.3(ZNF354A):c.502T>C (p.Phe168Leu)	ZNF354A (F126L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195359	NM_005649.3(ZNF354A):c.433G>C (p.Val145Leu)	ZNF354A (V145L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195358	NM_005649.3(ZNF354A):c.337A>T (p.Asn113Tyr)	ZNF354A (N113Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195357	NM_005649.3(ZNF354A):c.316G>A (p.Gly106Arg)	ZNF354A (G64R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488228	NM_005649.3(ZNF354A):c.305C>T (p.Ser102Phe)	ZNF354A (S60F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204185	NM_005649.3(ZNF354A):c.290C>T (p.Thr97Met)	ZNF354A (T97M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349722	NM_005649.3(ZNF354A):c.242G>A (p.Gly81Asp)	ZNF354A (G39D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195356	NM_005649.3(ZNF354A):c.204A>T (p.Gln68His)	ZNF354A (Q68H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511835	NM_005649.3(ZNF354A):c.184G>C (p.Val62Leu)	ZNF354A (V20L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468756	NM_005649.3(ZNF354A):c.111C>G (p.Asn37Lys)	ZNF354A (N37K)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2212896	NM_005649.3(ZNF354A):c.44C>T (p.Thr15Met)	ZNF354A (T15M)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance

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Items: 31