ClinVar for Gene (Select 8313) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3379229	NM_004655.4(AXIN2):c.2237+9C>T	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3379228	NM_004655.4(AXIN2):c.1071C>T (p.Arg357=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379227	NM_004655.4(AXIN2):c.2208C>A (p.Pro736=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379221	NM_004655.4(AXIN2):c.1200+6G>T	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3379217	NM_004655.4(AXIN2):c.2289G>A (p.Glu763=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379216	NM_004655.4(AXIN2):c.1201-11T>C	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3379210	NM_004655.4(AXIN2):c.1362_1365delinsGCCG (p.Ser454_Pro455=)	AXIN2	Indel (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379208	NM_004655.4(AXIN2):c.1908-7dup	AXIN2	Duplication (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3379201	NM_004655.4(AXIN2):c.1713-12G>T	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3379186	NM_004655.4(AXIN2):c.1305G>C (p.Pro435=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379177	NM_004655.4(AXIN2):c.2406-4dup	AXIN2	Duplication (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3379176	NM_004655.4(AXIN2):c.1712+9C>G	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3379167	NM_004655.4(AXIN2):c.2280G>A (p.Gln760=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379165	NM_004655.4(AXIN2):c.8_9dup	AXIN2	Duplication (3 prime UTR variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379158	NM_004655.4(AXIN2):c.1668A>G (p.Lys556=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379155	NM_004655.4(AXIN2):c.1884G>C (p.Arg628=)	AXIN2	Single nucleotide variant (synonymous variant +1 more)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379153	NM_004655.4(AXIN2):c.1731C>G (p.Thr577=)	AXIN2	Single nucleotide variant (synonymous variant +1 more)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379151	NM_004655.4(AXIN2):c.2301T>G (p.Thr767=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379147	NM_004655.4(AXIN2):c.1911C>G (p.Ala637=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379130	NM_004655.4(AXIN2):c.1347C>A (p.Thr449=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379127	NM_004655.4(AXIN2):c.2141+7G>A	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3379126	NM_004655.4(AXIN2):c.*9dup	AXIN2	Duplication (3 prime UTR variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379124	NM_004655.4(AXIN2):c.1350T>C (p.Pro450=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379120	NM_004655.4(AXIN2):c.2439C>A (p.Ala813=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379118	NM_004655.4(AXIN2):c.2238-10T>C	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3379113	NM_004655.4(AXIN2):c.1593C>A (p.Ile531=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379111	NM_004655.4(AXIN2):c.2406-15G>C	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3379099	NM_004655.4(AXIN2):c.2409T>C (p.Tyr803=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379097	NM_004655.4(AXIN2):c.1200+8G>C	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3379090	NM_004655.4(AXIN2):c.2484C>G (p.Leu828=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379089	NM_004655.4(AXIN2):c.2259G>A (p.Leu753=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379088	NM_004655.4(AXIN2):c.1907+7A>C	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3379081	NM_004655.4(AXIN2):c.1060-5T>C	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3379075	NM_004655.4(AXIN2):c.1506C>T (p.Gly502=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379074	NM_004655.4(AXIN2):c.*4C>T	AXIN2	Single nucleotide variant (3 prime UTR variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379072	NM_004655.4(AXIN2):c.1386_1389delinsTCGA (p.Pro462_Arg463=)	AXIN2	Indel (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379069	NM_004655.4(AXIN2):c.1920A>C (p.Thr640=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379067	NM_004655.4(AXIN2):c.1060-19_1060-17delinsCCT	AXIN2	Indel (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3379063	NM_004655.4(AXIN2):c.*8G>A	AXIN2	Single nucleotide variant (3 prime UTR variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379062	NM_004655.4(AXIN2):c.2475G>A (p.Glu825=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379059	NM_004655.4(AXIN2):c.1060-20_1060-17delinsCTCT	AXIN2	Indel (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3379054	NM_004655.4(AXIN2):c.1911C>A (p.Ala637=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379047	NM_004655.4(AXIN2):c.1140G>A (p.Lys380=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379042	NM_004655.4(AXIN2):c.1614G>C (p.Arg538=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379038	NM_004655.4(AXIN2):c.2238-4dup	AXIN2	Duplication (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3379029	NM_004655.4(AXIN2):c.1908-4T>C	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3379027	NM_004655.4(AXIN2):c.1197A>G (p.Arg399=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379026	NM_004655.4(AXIN2):c.1060-7C>T	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3379025	NM_004655.4(AXIN2):c.2531G>A (p.Ter844=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379022	NM_004655.4(AXIN2):c.2062_2064delinsTTA (p.Leu688=)	AXIN2	Indel (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379019	NM_004655.4(AXIN2):c.1683T>C (p.Ala561=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379017	NM_004655.4(AXIN2):c.2286T>C (p.Ser762=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379016	NM_004655.4(AXIN2):c.1713-10T>C	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3379015	NM_004655.4(AXIN2):c.*9G>T	AXIN2	Single nucleotide variant (3 prime UTR variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379005	NM_004655.4(AXIN2):c.2154C>G (p.Ala718=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379002	NM_004655.4(AXIN2):c.1386_1389delinsTCGT (p.Pro462_Arg463=)	AXIN2	Indel (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3379000	NM_004655.4(AXIN2):c.2124G>T (p.Ser708=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3378997	NM_004655.4(AXIN2):c.1500C>G (p.Leu500=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3378996	NM_004655.4(AXIN2):c.1713-7C>T	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3378995	NM_004655.4(AXIN2):c.1908-20T>C	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3378994	NM_004655.4(AXIN2):c.2070A>C (p.Pro690=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3378992	NM_004655.4(AXIN2):c.1143G>A (p.Leu381=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3378991	NM_004655.4(AXIN2):c.2142-6C>T	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3378987	NM_004655.4(AXIN2):c.1851G>A (p.Gln617=)	AXIN2	Single nucleotide variant (synonymous variant +1 more)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3378985	NM_004655.4(AXIN2):c.2405+9C>T	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3378979	NM_004655.4(AXIN2):c.1302C>T (p.Asp434=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3378975	NM_004655.4(AXIN2):c.1060-15T>C	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3378974	NM_004655.4(AXIN2):c.1515T>C (p.Phe505=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3378973	NM_004655.4(AXIN2):c.1359G>A (p.Gln453=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3378972	NM_004655.4(AXIN2):c.2112A>C (p.Leu704=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3378971	NM_004655.4(AXIN2):c.2142-17C>T	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3378970	NM_004655.4(AXIN2):c.2265T>C (p.Gly755=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3378969	NM_004655.4(AXIN2):c.*8G>C	AXIN2	Single nucleotide variant (3 prime UTR variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3378968	NM_004655.4(AXIN2):c.*2C>T	AXIN2	Single nucleotide variant (3 prime UTR variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3378967	NM_004655.4(AXIN2):c.2406-14G>T	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3378966	NM_004655.4(AXIN2):c.2406-17T>C	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3378964	NM_004655.4(AXIN2):c.*10T>A	AXIN2	Single nucleotide variant (3 prime UTR variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3378962	NM_004655.4(AXIN2):c.1512C>G (p.Gly504=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3378961	NM_004655.4(AXIN2):c.1185G>C (p.Leu395=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3378958	NM_004655.4(AXIN2):c.2250A>G (p.Pro750=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3378957	NM_004655.4(AXIN2):c.2406-16T>C	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3378956	NM_004655.4(AXIN2):c.*6G>C	AXIN2	Single nucleotide variant (3 prime UTR variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3378954	NM_004655.4(AXIN2):c.1200+7C>A	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3378951	NM_004655.4(AXIN2):c.1984C>T (p.Leu662=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3378950	NM_004655.4(AXIN2):c.1737C>G (p.Pro579=)	AXIN2	Single nucleotide variant (synonymous variant +1 more)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3378948	NM_004655.4(AXIN2):c.1713-4A>T	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3378946	NM_004655.4(AXIN2):c.1971C>G (p.Ala657=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3378945	NM_004655.4(AXIN2):c.1060-11A>C	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3378944	NM_004655.4(AXIN2):c.2406-19T>C	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3378943	NM_004655.4(AXIN2):c.1449C>G (p.Pro483=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3378940	NM_004655.4(AXIN2):c.1365_1368delinsGGGT (p.Pro455_Gly456=)	AXIN2	Indel (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3378936	NM_004655.4(AXIN2):c.1947C>T (p.Ala649=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3378935	NM_004655.4(AXIN2):c.1443C>G (p.Leu481=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3378931	NM_004655.4(AXIN2):c.1338C>G (p.Val446=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3378928	NM_004655.4(AXIN2):c.1401G>C (p.Pro467=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3370962	NM_004655.4(AXIN2):c.2237+2T>C	AXIN2	Single nucleotide variant (splice donor variant)	not provided	GUncertain significance
Select item 3370565	NM_004655.4(AXIN2):c.898A>G (p.Ser300Gly)	AXIN2 (S300G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3367901	NM_004655.4(AXIN2):c.1463C>G (p.Pro488Arg)	AXIN2 (P488R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3366118	NM_004655.4(AXIN2):c.1387C>A (p.Arg463Ser)	AXIN2 (R463S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3365040	NM_004655.4(AXIN2):c.275C>G (p.Ala92Gly)	AXIN2 (A92G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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