ADNP2[gene] and "single gene"[properties] - ClinVar

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Items: 83

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3089924	NM_014913.4(ADNP2):c.64A>G (p.Ile22Val)	ADNP2 (I22V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259277	NM_014913.4(ADNP2):c.89G>A (p.Ser30Asn)	ADNP2 (S30N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3273346	NM_014913.4(ADNP2):c.144T>G (p.Phe48Leu)	ADNP2 (F48L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089738	NM_014913.4(ADNP2):c.155C>T (p.Ser52Leu)	ADNP2 (S52L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512776	NM_014913.4(ADNP2):c.161G>T (p.Gly54Val)	ADNP2 (G54V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2603444	NM_014913.4(ADNP2):c.166G>A (p.Val56Ile)	ADNP2 (V56I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3089755	NM_014913.4(ADNP2):c.185C>A (p.Ser62Tyr)	ADNP2 (S62Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538820	NM_014913.4(ADNP2):c.253C>T (p.Leu85Phe)	ADNP2 (L85F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089809	NM_014913.4(ADNP2):c.269A>T (p.Asn90Ile)	ADNP2 (N90I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089811	NM_014913.4(ADNP2):c.278A>G (p.His93Arg)	ADNP2 (H93R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089823	NM_014913.4(ADNP2):c.281G>A (p.Arg94His)	ADNP2 (R94H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2236643	NM_014913.4(ADNP2):c.291A>T (p.Glu97Asp)	ADNP2 (E97D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3273405	NM_014913.4(ADNP2):c.362G>A (p.Gly121Glu)	ADNP2 (G121E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2531071	NM_014913.4(ADNP2):c.389C>G (p.Pro130Arg)	ADNP2 (P130R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392161	NM_014913.4(ADNP2):c.394C>T (p.Arg132Trp)	ADNP2 (R132W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2237557	NM_014913.4(ADNP2):c.410A>G (p.Tyr137Cys)	ADNP2 (Y137C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295052	NM_014913.4(ADNP2):c.584G>A (p.Gly195Asp)	ADNP2 (G195D)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3089915	NM_014913.4(ADNP2):c.604G>A (p.Asp202Asn)	ADNP2 (D202N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618945	NM_014913.4(ADNP2):c.625A>G (p.Ile209Val)	ADNP2 (I209V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2288102	NM_014913.4(ADNP2):c.626T>C (p.Ile209Thr)	ADNP2 (I209T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396685	NM_014913.4(ADNP2):c.668A>G (p.Asn223Ser)	ADNP2 (N223S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225556	NM_014913.4(ADNP2):c.791C>T (p.Thr264Met)	ADNP2 (T264M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3273411	NM_014913.4(ADNP2):c.796A>G (p.Ile266Val)	ADNP2 (I266V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089933	NM_014913.4(ADNP2):c.859G>A (p.Ala287Thr)	ADNP2 (A287T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089942	NM_014913.4(ADNP2):c.970C>G (p.Pro324Ala)	ADNP2 (P324A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537498	NM_014913.4(ADNP2):c.970C>T (p.Pro324Ser)	ADNP2 (P324S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315244	NM_014913.4(ADNP2):c.976G>C (p.Ala326Pro)	ADNP2 (A326P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248528	NM_014913.4(ADNP2):c.991A>G (p.Met331Val)	ADNP2 (M331V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2593015	NM_014913.4(ADNP2):c.1078G>A (p.Gly360Arg)	ADNP2 (G360R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274590	NM_014913.4(ADNP2):c.1104T>A (p.Asn368Lys)	ADNP2 (N368K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089721	NM_014913.4(ADNP2):c.1128G>T (p.Gln376His)	ADNP2 (Q376H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3273336	NM_014913.4(ADNP2):c.1186G>C (p.Val396Leu)	ADNP2 (V396L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089725	NM_014913.4(ADNP2):c.1279C>T (p.Pro427Ser)	ADNP2 (P427S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089727	NM_014913.4(ADNP2):c.1334C>T (p.Pro445Leu)	ADNP2 (P445L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331692	NM_014913.4(ADNP2):c.1352C>G (p.Ala451Gly)	ADNP2 (A451G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529074	NM_014913.4(ADNP2):c.1402G>A (p.Gly468Arg)	ADNP2 (G468R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2269396	NM_014913.4(ADNP2):c.1429C>T (p.Pro477Ser)	ADNP2 (P477S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2267046	NM_014913.4(ADNP2):c.1481C>T (p.Pro494Leu)	ADNP2 (P494L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089741	NM_014913.4(ADNP2):c.1588G>C (p.Ala530Pro)	ADNP2 (A530P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527204	NM_014913.4(ADNP2):c.1696C>A (p.Gln566Lys)	ADNP2 (Q566K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2234317	NM_014913.4(ADNP2):c.1891C>T (p.Leu631Phe)	ADNP2 (L631F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207156	NM_014913.4(ADNP2):c.1907C>A (p.Pro636Gln)	ADNP2 (P636Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409867	NM_014913.4(ADNP2):c.1972G>A (p.Gly658Ser)	ADNP2 (G658S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2552966	NM_014913.4(ADNP2):c.2050A>C (p.Asn684His)	ADNP2 (N684H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2648838	NM_014913.4(ADNP2):c.2112G>A (p.Pro704=)	ADNP2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3089773	NM_014913.4(ADNP2):c.2117A>G (p.Asn706Ser)	ADNP2 (N706S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2234266	NM_014913.4(ADNP2):c.2197G>T (p.Ala733Ser)	ADNP2 (A733S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2307088	NM_014913.4(ADNP2):c.2231A>G (p.Glu744Gly)	ADNP2 (E744G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2294267	NM_014913.4(ADNP2):c.2401A>G (p.Met801Val)	ADNP2 (M801V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3089787	NM_014913.4(ADNP2):c.2510G>A (p.Arg837Gln)	ADNP2 (R837Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089792	NM_014913.4(ADNP2):c.2527A>G (p.Ile843Val)	ADNP2 (I843V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089800	NM_014913.4(ADNP2):c.2606G>A (p.Ser869Asn)	ADNP2 (S869N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274327	NM_014913.4(ADNP2):c.2648C>T (p.Pro883Leu)	ADNP2 (P883L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2648839	NM_014913.4(ADNP2):c.2796C>T (p.Ala932=)	ADNP2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2332737	NM_014913.4(ADNP2):c.2797G>A (p.Val933Ile)	ADNP2 (V933I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2352960	NM_014913.4(ADNP2):c.2809C>T (p.Arg937Cys)	ADNP2 (R937C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3273395	NM_014913.4(ADNP2):c.2822C>T (p.Ala941Val)	ADNP2 (A941V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089825	NM_014913.4(ADNP2):c.2827A>G (p.Lys943Glu)	ADNP2 (K943E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620993	NM_014913.4(ADNP2):c.2835C>G (p.Ser945Arg)	ADNP2 (S945R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556130	NM_014913.4(ADNP2):c.2857C>T (p.Pro953Ser)	ADNP2 (P953S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2298766	NM_014913.4(ADNP2):c.2884C>T (p.Leu962Phe)	ADNP2 (L962F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3273357	NM_014913.4(ADNP2):c.2917A>G (p.Ser973Gly)	ADNP2 (S973G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257040	NM_014913.4(ADNP2):c.2947G>A (p.Gly983Ser)	ADNP2 (G983S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285975	NM_014913.4(ADNP2):c.2951A>G (p.His984Arg)	ADNP2 (H984R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089845	NM_014913.4(ADNP2):c.2962G>A (p.Glu988Lys)	ADNP2 (E988K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524477	NM_014913.4(ADNP2):c.2978G>A (p.Gly993Glu)	ADNP2 (G993E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521901	NM_014913.4(ADNP2):c.2989C>T (p.Pro997Ser)	ADNP2 (P997S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511831	NM_014913.4(ADNP2):c.3007G>C (p.Asp1003His)	ADNP2 (D1003H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089853	NM_014913.4(ADNP2):c.3008A>G (p.Asp1003Gly)	ADNP2 (D1003G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488567	NM_014913.4(ADNP2):c.3022C>G (p.Pro1008Ala)	ADNP2 (P1008A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478911	NM_014913.4(ADNP2):c.3035C>G (p.Thr1012Arg)	ADNP2 (T1012R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2263117	NM_014913.4(ADNP2):c.3035C>T (p.Thr1012Met)	ADNP2 (T1012M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299078	NM_014913.4(ADNP2):c.3066T>A (p.Asn1022Lys)	ADNP2 (N1022K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3273368	NM_014913.4(ADNP2):c.3076A>G (p.Thr1026Ala)	ADNP2 (T1026A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613007	NM_014913.4(ADNP2):c.3088A>G (p.Ile1030Val)	ADNP2 (I1030V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089884	NM_014913.4(ADNP2):c.3124G>C (p.Asp1042His)	ADNP2 (D1042H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458276	NM_014913.4(ADNP2):c.3131A>G (p.Lys1044Arg)	ADNP2 (K1044R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598948	NM_014913.4(ADNP2):c.3146G>A (p.Arg1049His)	ADNP2 (R1049H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089898	NM_014913.4(ADNP2):c.3233C>T (p.Ser1078Leu)	ADNP2 (S1078L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389631	NM_014913.4(ADNP2):c.3239T>C (p.Phe1080Ser)	ADNP2 (F1080S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3273380	NM_014913.4(ADNP2):c.3281G>C (p.Arg1094Thr)	ADNP2 (R1094T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3273386	NM_014913.4(ADNP2):c.3307A>G (p.Lys1103Glu)	ADNP2 (K1103E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2568635	NM_014913.4(ADNP2):c.3323C>T (p.Ser1108Phe)	ADNP2 (S1108F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 83