"Ambry Genetics"[submitter] AND "ZFP69B"[gene] - ClinVar

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Items: 30

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3334523	NM_023070.3(ZFP69B):c.44C>T (p.Thr15Ile)	LOC126805713, ZFP69B (T15I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2531810	NM_023070.3(ZFP69B):c.59G>A (p.Arg20His)	LOC126805713, ZFP69B (R20H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3334522	NM_023070.3(ZFP69B):c.161G>A (p.Gly54Asp)	ZFP69B (G54D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193202	NM_023070.3(ZFP69B):c.268C>A (p.Gln90Lys)	ZFP69B (Q90K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621151	NM_023070.3(ZFP69B):c.275C>A (p.Ala92Asp)	ZFP69B (A92D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2475337	NM_023070.3(ZFP69B):c.299G>A (p.Arg100Gln)	ZFP69B (R100Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543981	NM_023070.3(ZFP69B):c.359C>T (p.Pro120Leu)	ZFP69B (P120L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223084	NM_023070.3(ZFP69B):c.364G>A (p.Val122Met)	ZFP69B (V122M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193203	NM_023070.3(ZFP69B):c.383A>G (p.Lys128Arg)	ZFP69B (K128R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334521	NM_023070.3(ZFP69B):c.409A>G (p.Arg137Gly)	ZFP69B (R137G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193204	NM_023070.3(ZFP69B):c.416T>C (p.Ile139Thr)	ZFP69B (I139T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193205	NM_023070.3(ZFP69B):c.485T>G (p.Ile162Ser)	ZFP69B (I162S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347860	NM_023070.3(ZFP69B):c.494A>G (p.Glu165Gly)	ZFP69B (E165G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599559	NM_023070.3(ZFP69B):c.518T>C (p.Met173Thr)	ZFP69B (M173T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539996	NM_023070.3(ZFP69B):c.542G>A (p.Ser181Asn)	ZFP69B (S181N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348001	NM_023070.3(ZFP69B):c.608G>T (p.Arg203Ile)	ZFP69B (R203I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403715	NM_023070.3(ZFP69B):c.636G>A (p.Met212Ile)	ZFP69B (M212I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3193207	NM_023070.3(ZFP69B):c.694A>G (p.Ile232Val)	ZFP69B (I232V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260054	NM_023070.3(ZFP69B):c.884C>T (p.Thr295Ile)	ZFP69B (T295I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618704	NM_023070.3(ZFP69B):c.928A>G (p.Lys310Glu)	ZFP69B (K310E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543982	NM_023070.3(ZFP69B):c.967A>G (p.Ile323Val)	ZFP69B (I323V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342891	NM_023070.3(ZFP69B):c.980G>T (p.Arg327Ile)	ZFP69B (R327I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314819	NM_023070.3(ZFP69B):c.1093T>G (p.Cys365Gly)	ZFP69B (C365G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520940	NM_023070.3(ZFP69B):c.1162G>A (p.Glu388Lys)	ZFP69B (E388K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287565	NM_023070.3(ZFP69B):c.1225C>T (p.His409Tyr)	ZFP69B (H409Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207223	NM_023070.3(ZFP69B):c.1256A>G (p.Tyr419Cys)	ZFP69B (Y419C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193200	NM_023070.3(ZFP69B):c.1289A>G (p.His430Arg)	ZFP69B (H430R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478946	NM_023070.3(ZFP69B):c.1316G>A (p.Arg439Lys)	ZFP69B (R439K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367984	NM_023070.3(ZFP69B):c.1529A>T (p.Lys510Ile)	ZFP69B (K510I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517507	NM_023070.3(ZFP69B):c.1574A>C (p.His525Pro)	ZFP69B (H525P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 30