"Ambry Genetics"[submitter] AND "ZSCAN32"[gene] - ClinVar

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Items: 30

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2233940	NM_001284527.2(ZSCAN32):c.2033G>A (p.Arg678His)	ZSCAN32 (R466H +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2342837	NM_001284527.2(ZSCAN32):c.1999G>C (p.Glu667Gln)	ZSCAN32 (E378Q +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2359027	NM_001284527.2(ZSCAN32):c.1994A>C (p.His665Pro)	ZSCAN32 (H376P +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2260296	NM_001284527.2(ZSCAN32):c.1986G>C (p.Arg662Ser)	ZSCAN32 (R589S +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2589335	NM_001284527.2(ZSCAN32):c.1913G>A (p.Cys638Tyr)	ZSCAN32 (C505Y +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2303433	NM_001284527.2(ZSCAN32):c.1907C>T (p.Ala636Val)	ZSCAN32 (A424V +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2481465	NM_001284527.2(ZSCAN32):c.1837A>G (p.Arg613Gly)	ZSCAN32 (R324G +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2476136	NM_001284527.2(ZSCAN32):c.1819T>C (p.Cys607Arg)	ZSCAN32 (C534R +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2476135	NM_001284527.2(ZSCAN32):c.1818G>T (p.Gln606His)	ZSCAN32 (Q473H +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2535768	NM_001284527.2(ZSCAN32):c.1801G>A (p.Gly601Arg)	ZSCAN32 (G312R +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2269246	NM_001284527.2(ZSCAN32):c.1772G>A (p.Ser591Asn)	ZSCAN32 (S302N +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2323416	NM_001284527.2(ZSCAN32):c.1730A>G (p.Tyr577Cys)	ZSCAN32 (Y504C +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2356964	NM_001284527.2(ZSCAN32):c.1682G>A (p.Arg561His)	ZSCAN32 (R428H +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2323570	NM_001284527.2(ZSCAN32):c.1640A>T (p.Lys547Met)	ZSCAN32 (K258M +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2319511	NM_001284527.2(ZSCAN32):c.1557A>C (p.Lys519Asn)	ZSCAN32 (K230N +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2282818	NM_001284527.2(ZSCAN32):c.1418A>C (p.Glu473Ala)	ZSCAN32 (E261A +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2484371	NM_001284527.2(ZSCAN32):c.1396A>G (p.Arg466Gly)	ZSCAN32 (R466G +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2343218	NM_001284527.2(ZSCAN32):c.1388G>A (p.Arg463Lys)	ZSCAN32 (R390K +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2491536	NM_001284527.2(ZSCAN32):c.1361G>A (p.Gly454Asp)	ZSCAN32 (G165D +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2343217	NM_001284527.2(ZSCAN32):c.1324T>C (p.Ser442Pro)	ZSCAN32 (S230P +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2302417	NM_001284527.2(ZSCAN32):c.1181C>A (p.Pro394His)	ZSCAN32 (P261H +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2256739	NM_001284527.2(ZSCAN32):c.1099A>G (p.Asn367Asp)	ZSCAN32 (N155D +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2261154	NM_001284527.2(ZSCAN32):c.986G>C (p.Cys329Ser)	ZSCAN32 (C196S +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2282230	NM_001284527.2(ZSCAN32):c.919C>T (p.Arg307Cys)	ZSCAN32 (R174C +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2380263	NM_001284527.2(ZSCAN32):c.901C>T (p.Arg301Trp)	ZSCAN32 (R301W +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2263273	NM_001284527.2(ZSCAN32):c.889C>G (p.Gln297Glu)	ZSCAN32 (Q297E +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2537496	NM_001284527.2(ZSCAN32):c.835A>T (p.Thr279Ser)	ZSCAN32 (T146S +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2537495	NM_001284527.2(ZSCAN32):c.834G>T (p.Gln278His)	ZSCAN32 (Q145H +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2301398	NM_001284527.2(ZSCAN32):c.832C>A (p.Gln278Lys)	ZSCAN32 (Q145K +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2359368	NM_001284527.2(ZSCAN32):c.727A>T (p.Arg243Trp)	ZSCAN32 (R242W +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

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Items: 30