"Ambry Genetics"[submitter] AND "ZNF79"[gene] - ClinVar

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Items: 41

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2274714	NM_007135.3(ZNF79):c.28C>T (p.Pro10Ser)	ZNF79 (P10S)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2324296	NM_007135.3(ZNF79):c.40C>G (p.Leu14Val)	ZNF79 (L14V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3198418	NM_007135.3(ZNF79):c.43C>T (p.Pro15Ser)	ZNF79 (P15S)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3198409	NM_007135.3(ZNF79):c.103C>T (p.Arg35Trp)	ZNF79 (R11W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198413	NM_007135.3(ZNF79):c.131C>T (p.Thr44Met)	ZNF79 (T20M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2402381	NM_007135.3(ZNF79):c.137C>G (p.Ala46Gly)	ZNF79 (A22G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2267629	NM_007135.3(ZNF79):c.203C>G (p.Pro68Arg)	ZNF79 (P68R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2231766	NM_007135.3(ZNF79):c.286G>T (p.Ala96Ser)	ZNF79 (A96S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2381080	NM_007135.3(ZNF79):c.298G>A (p.Glu100Lys)	ZNF79 (E76K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2225108	NM_007135.3(ZNF79):c.304G>A (p.Glu102Lys)	ZNF79 (E102K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2298690	NM_007135.3(ZNF79):c.305A>C (p.Glu102Ala)	ZNF79 (E102A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2227588	NM_007135.3(ZNF79):c.314G>A (p.Arg105Gln)	ZNF79 (R105Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2309674	NM_007135.3(ZNF79):c.320C>T (p.Pro107Leu)	ZNF79 (P107L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2338255	NM_007135.3(ZNF79):c.433A>G (p.Ser145Gly)	ZNF79 (S11G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198419	NM_007135.3(ZNF79):c.454A>T (p.Asn152Tyr)	ZNF79 (N18Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198420	NM_007135.3(ZNF79):c.463C>A (p.Pro155Thr)	ZNF79 (P155T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252858	NM_007135.3(ZNF79):c.473C>G (p.Ser158Cys)	ZNF79 (S134C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411002	NM_007135.3(ZNF79):c.515G>A (p.Cys172Tyr)	ZNF79 (C148Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358960	NM_007135.3(ZNF79):c.545C>T (p.Ser182Leu)	ZNF79 (S48L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198421	NM_007135.3(ZNF79):c.629A>T (p.Gln210Leu)	ZNF79 (Q186L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311452	NM_007135.3(ZNF79):c.670A>G (p.Ser224Gly)	ZNF79 (S90G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198422	NM_007135.3(ZNF79):c.743C>A (p.Pro248His)	ZNF79 (P224H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304360	NM_007135.3(ZNF79):c.815C>G (p.Thr272Ser)	ZNF79 (T248S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386153	NM_007135.3(ZNF79):c.841G>A (p.Glu281Lys)	ZNF79 (E281K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261749	NM_007135.3(ZNF79):c.850A>G (p.Lys284Glu)	ZNF79 (K150E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198423	NM_007135.3(ZNF79):c.871G>A (p.Ala291Thr)	ZNF79 (A291T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198424	NM_007135.3(ZNF79):c.932G>A (p.Gly311Glu)	ZNF79 (G287E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198410	NM_007135.3(ZNF79):c.1042T>A (p.Phe348Ile)	ZNF79 (F214I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198411	NM_007135.3(ZNF79):c.1111A>T (p.Ser371Cys)	ZNF79 (S347C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470737	NM_007135.3(ZNF79):c.1141A>G (p.Arg381Gly)	ZNF79 (R381G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198412	NM_007135.3(ZNF79):c.1177G>A (p.Glu393Lys)	ZNF79 (E259K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551249	NM_007135.3(ZNF79):c.1190C>G (p.Ala397Gly)	ZNF79 (A397G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373311	NM_007135.3(ZNF79):c.1225A>G (p.Lys409Glu)	ZNF79 (K275E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469883	NM_007135.3(ZNF79):c.1237G>A (p.Gly413Arg)	ZNF79 (G413R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331946	NM_007135.3(ZNF79):c.1246C>T (p.Pro416Ser)	ZNF79 (P282S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2472068	NM_007135.3(ZNF79):c.1300C>T (p.Arg434Trp)	ZNF79 (R410W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198414	NM_007135.3(ZNF79):c.1397T>C (p.Ile466Thr)	ZNF79 (I442T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198415	NM_007135.3(ZNF79):c.1408G>A (p.Val470Met)	ZNF79 (V336M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198416	NM_007135.3(ZNF79):c.1448G>A (p.Arg483Gln)	ZNF79 (R459Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384281	NM_007135.3(ZNF79):c.1475A>C (p.Gln492Pro)	ZNF79 (Q468P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517134	NM_007135.3(ZNF79):c.1486G>A (p.Ala496Thr)	ZNF79 (A362T +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign

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Items: 41