ClinVar for MedGen (Select 324868) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3065145	NM_004655.4(AXIN2):c.737C>T (p.Thr246Ile)	AXIN2 (T246I)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3019222	NM_004655.4(AXIN2):c.641G>T (p.Gly214Val)	AXIN2 (G214V)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 3017445	NM_004655.4(AXIN2):c.1329G>A (p.Leu443=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3017298	NM_004655.4(AXIN2):c.1847C>G (p.Ser616Trp)	AXIN2 (S616W)	Single nucleotide variant (missense variant +1 more)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 3015848	NM_004655.4(AXIN2):c.1832A>G (p.Glu611Gly)	AXIN2 (E611G)	Single nucleotide variant (missense variant +1 more)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 3015806	NM_004655.4(AXIN2):c.816-13A>G	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3014267	NM_004655.4(AXIN2):c.16T>C (p.Leu6=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3013298	NM_004655.4(AXIN2):c.2500C>G (p.Arg834Gly)	AXIN2 (R834G +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 3011351	NM_004655.4(AXIN2):c.2464T>C (p.Trp822Arg)	AXIN2 (W757R +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 3010184	NM_004655.4(AXIN2):c.1320C>A (p.Asp440Glu)	AXIN2 (D440E)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 3010114	NM_004655.4(AXIN2):c.1168A>T (p.Ser390Cys)	AXIN2 (S390C)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 3009825	NM_004655.4(AXIN2):c.1507A>G (p.Lys503Glu)	AXIN2 (K503E)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 3006086	NM_004655.4(AXIN2):c.2172G>A (p.Arg724=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2999750	NM_004655.4(AXIN2):c.1310C>G (p.Thr437Arg)	AXIN2 (T437R)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2998670	NM_004655.4(AXIN2):c.1102G>T (p.Ala368Ser)	AXIN2 (A368S)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2998258	NM_004655.4(AXIN2):c.50T>A (p.Phe17Tyr)	AXIN2 (F17Y)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2997608	NM_004655.4(AXIN2):c.250T>C (p.Ser84Pro)	AXIN2 (S84P)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2996485	NM_004655.4(AXIN2):c.2237+7G>A	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2990313	NM_004655.4(AXIN2):c.2009C>G (p.Pro670Arg)	AXIN2 (P670R +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2989264	NM_004655.4(AXIN2):c.763C>T (p.Leu255=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2988595	NM_004655.4(AXIN2):c.81A>G (p.Pro27=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2981321	NM_004655.4(AXIN2):c.761C>T (p.Thr254Ile)	AXIN2 (T254I)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2981255	NM_004655.4(AXIN2):c.742G>A (p.Val248Ile)	AXIN2 (V248I)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2980801	NM_004655.4(AXIN2):c.298G>A (p.Glu100Lys)	AXIN2 (E100K)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2974635	NM_004655.4(AXIN2):c.798T>G (p.Thr266=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2973252	NM_004655.4(AXIN2):c.1027G>A (p.Ala343Thr)	AXIN2 (A343T)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2972994	NM_004655.4(AXIN2):c.403T>C (p.Tyr135His)	AXIN2 (Y135H)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2971833	NM_004655.4(AXIN2):c.1941G>A (p.Glu647=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2971371	NM_004655.4(AXIN2):c.412T>C (p.Tyr138His)	AXIN2 (Y138H)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2970579	NM_004655.4(AXIN2):c.431T>C (p.Ile144Thr)	AXIN2 (I144T)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2970528	NM_004655.4(AXIN2):c.1526A>G (p.Gln509Arg)	AXIN2 (Q509R)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2966745	NM_004655.4(AXIN2):c.123C>T (p.Gly41=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2964359	NM_004655.4(AXIN2):c.1648T>C (p.Tyr550His)	AXIN2 (Y550H)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2961780	NM_004655.4(AXIN2):c.1245G>C (p.Glu415Asp)	AXIN2 (E415D)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2961765	NM_004655.4(AXIN2):c.979G>A (p.Val327Met)	AXIN2 (V327M)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2959851	NM_004655.4(AXIN2):c.8G>A (p.Ser3Asn)	AXIN2 (S3N)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2958937	NM_004655.4(AXIN2):c.966T>C (p.Ile322=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2957928	NM_004655.4(AXIN2):c.587A>G (p.Tyr196Cys)	AXIN2 (Y196C)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2956404	NM_004655.4(AXIN2):c.1593del (p.Ile531fs)	AXIN2 (I531fs)	Deletion (frameshift variant)	Oligodontia-cancer predisposition syndrome	GPathogenic
Select item 2918794	NM_004655.4(AXIN2):c.42C>T (p.Ser14=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2918162	NM_004655.4(AXIN2):c.255A>G (p.Leu85=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2918076	NM_004655.4(AXIN2):c.956+11T>C	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2917094	NM_004655.4(AXIN2):c.218C>T (p.Ser73Phe)	AXIN2 (S73F)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2916625	NM_004655.4(AXIN2):c.411G>A (p.Arg137=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2915594	NM_004655.4(AXIN2):c.1348C>G (p.Pro450Ala)	AXIN2 (P450A)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2914963	NM_004655.4(AXIN2):c.1570G>T (p.Val524Phe)	AXIN2 (V524F)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2913000	NM_004655.4(AXIN2):c.2433G>C (p.Glu811Asp)	AXIN2 (E746D +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2911240	NM_004655.4(AXIN2):c.1060-18C>T	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2907261	NM_004655.4(AXIN2):c.694GAG[1] (p.Glu233del)	AXIN2 (E233del)	Microsatellite (inframe_deletion)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2906835	NM_004655.4(AXIN2):c.2310C>T (p.Phe770=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2906013	NM_004655.4(AXIN2):c.392C>G (p.Ala131Gly)	AXIN2 (A131G)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2902186	NM_004655.4(AXIN2):c.1059+15G>A	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2897530	NM_004655.4(AXIN2):c.66G>T (p.Pro22=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2896661	NM_004655.4(AXIN2):c.1385C>T (p.Pro462Leu)	AXIN2 (P462L)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2896490	NM_004655.4(AXIN2):c.577T>A (p.Ser193Thr)	AXIN2 (S193T)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2895579	NM_004655.4(AXIN2):c.265C>A (p.Gln89Lys)	AXIN2 (Q89K)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2893249	NM_004655.4(AXIN2):c.855A>G (p.Ile285Met)	AXIN2 (I285M)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2890152	NM_004655.4(AXIN2):c.1712+12G>C	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2890111	NM_004655.4(AXIN2):c.1907+8C>T	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2888638	NM_004655.4(AXIN2):c.2142-17C>G	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2885492	NM_004655.4(AXIN2):c.1825C>A (p.Pro609Thr)	AXIN2 (P609T)	Single nucleotide variant (missense variant +1 more)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2885308	NM_004655.4(AXIN2):c.38C>T (p.Pro13Leu)	AXIN2 (P13L)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2883209	NM_004655.4(AXIN2):c.957-17C>T	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2883123	NM_004655.4(AXIN2):c.1778C>T (p.Pro593Leu)	AXIN2 (P593L)	Single nucleotide variant (missense variant +1 more)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2882428	NM_004655.4(AXIN2):c.643C>T (p.Leu215Phe)	AXIN2 (L215F)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2882033	NM_004655.4(AXIN2):c.1712+14G>T	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2881022	NM_004655.4(AXIN2):c.1059+10G>A	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2879323	NM_004655.4(AXIN2):c.995A>G (p.Gln332Arg)	AXIN2 (Q332R)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2877184	NM_004655.4(AXIN2):c.1200+8G>T	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2874296	NM_004655.4(AXIN2):c.1059+20A>C	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2871833	NM_004655.4(AXIN2):c.2142-19G>C	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2871428	NM_004655.4(AXIN2):c.1907+13dup	AXIN2	Duplication (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2871395	NM_004655.4(AXIN2):c.877C>T (p.Pro293Ser)	AXIN2 (P293S)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2871339	NM_004655.4(AXIN2):c.1907+13T>A	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2870224	NM_004655.4(AXIN2):c.664T>A (p.Cys222Ser)	AXIN2 (C222S)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2869217	NM_004655.4(AXIN2):c.1907+10G>T	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2867537	NM_004655.4(AXIN2):c.957-10T>G	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2867491	NM_004655.4(AXIN2):c.2528A>T (p.Asp843Val)	AXIN2 (D778V +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2865140	NM_004655.4(AXIN2):c.1370_1372dup (p.Val457_Gly458insVal)	AXIN2	Duplication (inframe_insertion)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2862752	NM_004655.4(AXIN2):c.1628_1630delinsTTT (p.Cys543_Pro544delinsPheSer)	AXIN2	Indel (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2862406	NM_004655.4(AXIN2):c.809G>A (p.Gly270Glu)	AXIN2 (G270E)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2861646	NM_004655.4(AXIN2):c.1759G>T (p.Glu587Ter)	AXIN2 (E587*)	Single nucleotide variant (nonsense +1 more)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2861040	NM_004655.4(AXIN2):c.168G>A (p.Arg56=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2860872	NM_004655.4(AXIN2):c.1084A>G (p.Met362Val)	AXIN2 (M362V)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2860570	NM_004655.4(AXIN2):c.629T>A (p.Met210Lys)	AXIN2 (M210K)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2860259	NM_004655.4(AXIN2):c.777G>T (p.Ala259=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2859708	NM_004655.4(AXIN2):c.1926G>A (p.Lys642=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2859625	NM_004655.4(AXIN2):c.199G>A (p.Gly67Arg)	AXIN2 (G67R)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2858749	NM_004655.4(AXIN2):c.1176G>C (p.Glu392Asp)	AXIN2 (E392D)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2858056	NM_004655.4(AXIN2):c.1474G>T (p.Ala492Ser)	AXIN2 (A492S)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2857836	NM_004655.4(AXIN2):c.1725C>A (p.Gly575=)	AXIN2	Single nucleotide variant (synonymous variant +1 more)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2857830	NM_004655.4(AXIN2):c.491A>G (p.Gln164Arg)	AXIN2 (Q164R)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2856488	NM_004655.4(AXIN2):c.317A>G (p.Asp106Gly)	AXIN2 (D106G)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2855924	NM_004655.4(AXIN2):c.1736C>A (p.Pro579His)	AXIN2 (P579H)	Single nucleotide variant (missense variant +1 more)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2855795	NM_004655.4(AXIN2):c.1281C>G (p.Pro427=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2855447	NM_004655.4(AXIN2):c.1820A>G (p.Gln607Arg)	AXIN2 (Q607R)	Single nucleotide variant (missense variant +1 more)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2854550	NM_004655.4(AXIN2):c.1695G>T (p.Met565Ile)	AXIN2 (M565I)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 2853551	NM_004655.4(AXIN2):c.1396_1447del (p.Ser466fs)	AXIN2 (S466fs)	Deletion (frameshift variant)	Oligodontia-cancer predisposition syndrome	GPathogenic
Select item 2853177	NM_004655.4(AXIN2):c.1533G>C (p.Thr511=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 2852588	NM_004655.4(AXIN2):c.2047C>A (p.Pro683Thr)	AXIN2 (P618T +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome	GUncertain significance

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