"GeneDx"[submitter] AND "AXIN2"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 382317	NM_004655.4(AXIN2):c.*5T>G	AXIN2	Single nucleotide variant (3 prime UTR variant)	not specified +1 more	GBenign/Likely benign
Select item 821430	NM_004655.4(AXIN2):c.2527G>A (p.Asp843Asn)	AXIN2 (D843N +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +3 more	GUncertain significance
Select item 511158	NM_004655.4(AXIN2):c.2526C>T (p.Ile842=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome +2 more	GBenign/Likely benign
Select item 419006	NM_004655.4(AXIN2):c.2522G>A (p.Arg841Gln)	AXIN2 (R841Q +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 127946	NM_004655.4(AXIN2):c.2521C>T (p.Arg841Trp)	AXIN2 (R841W +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 766674	NM_004655.4(AXIN2):c.2508G>A (p.Leu836=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 464615	NM_004655.4(AXIN2):c.2499C>A (p.Gly833=)	AXIN2	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign
Select item 939793	NM_004655.4(AXIN2):c.2490G>A (p.Met830Ile)	AXIN2 (M765I +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +1 more	GUncertain significance
Select item 572057	NM_004655.4(AXIN2):c.2489T>C (p.Met830Thr)	AXIN2 (M830T +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +2 more	GUncertain significance
Select item 509112	NM_004655.4(AXIN2):c.2487G>A (p.Pro829=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 747399	NM_004655.4(AXIN2):c.2478G>T (p.Thr826=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
Select item 408825	NM_004655.4(AXIN2):c.2477C>T (p.Thr826Met)	AXIN2 (T826M +1 more)	Single nucleotide variant (missense variant)	Colorectal cancer +3 more	GUncertain significance
Select item 571013	NM_004655.4(AXIN2):c.2472T>A (p.Asp824Glu)	AXIN2 (D824E +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 575631	NM_004655.4(AXIN2):c.2447C>T (p.Ala816Val)	AXIN2 (A816V +1 more)	Single nucleotide variant (missense variant)	Ovarian cancer +5 more	GConflicting classifications of pathogenicity
Select item 240015	NM_004655.4(AXIN2):c.2439C>T (p.Ala813=)	AXIN2	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 182020	NM_004655.4(AXIN2):c.2433G>A (p.Glu811=)	AXIN2	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 385118	NM_004655.4(AXIN2):c.2430T>C (p.Asp810=)	AXIN2	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign
Select item 127945	NM_004655.4(AXIN2):c.2428G>A (p.Asp810Asn)	AXIN2 (D810N +1 more)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 464610	NM_004655.4(AXIN2):c.2420A>C (p.Lys807Thr)	AXIN2 (K807T +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +3 more	GUncertain significance
Select item 240014	NM_004655.4(AXIN2):c.2406-8C>G	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome +4 more	GBenign/Likely benign
Select item 1196472	NM_004655.4(AXIN2):c.2406-284C>T	AXIN2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 679667	NM_004655.4(AXIN2):c.2405+209G>A	AXIN2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 675640	NM_004655.4(AXIN2):c.2405+180C>T	AXIN2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 676477	NM_004655.4(AXIN2):c.2405+125G>T	AXIN2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 415234	NM_004655.4(AXIN2):c.2405+7G>A	AXIN2	Single nucleotide variant (intron variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 408761	NM_004655.4(AXIN2):c.2405+4A>C	AXIN2	Single nucleotide variant (intron variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 234770	NM_004655.4(AXIN2):c.2405+4A>G	AXIN2	Single nucleotide variant (intron variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 380431	NM_004655.4(AXIN2):c.2403T>C (p.Tyr801=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GBenign/Likely benign
Select item 240013	NM_004655.4(AXIN2):c.2394G>A (p.Lys798=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome +2 more	GBenign/Likely benign
Select item 950630	NM_004655.4(AXIN2):c.2379G>C (p.Glu793Asp)	AXIN2 (E793D +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 464607	NM_004655.4(AXIN2):c.2347G>T (p.Ala783Ser)	AXIN2 (A783S +1 more)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 385102	NM_004655.4(AXIN2):c.2343G>A (p.Leu781=)	AXIN2	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 857128	NM_004655.4(AXIN2):c.2332C>T (p.Arg778Trp)	AXIN2 (R713W +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +2 more	GUncertain significance
Select item 418819	NM_004655.4(AXIN2):c.2326C>T (p.Pro776Ser)	AXIN2 (P776S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1789602	NM_004655.4(AXIN2):c.2323_2325delinsTTC (p.Ile775Phe)	AXIN2 (I710F +1 more)	Indel (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1045447	NM_004655.4(AXIN2):c.2320G>A (p.Glu774Lys)	AXIN2 (E774K +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +1 more	GUncertain significance
Select item 1306405	NM_004655.4(AXIN2):c.2304C>G (p.Tyr768Ter)	AXIN2 (Y703* +1 more)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 533171	NM_004655.4(AXIN2):c.2303A>T (p.Tyr768Phe)	AXIN2 (Y768F +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 1302086	NM_004655.4(AXIN2):c.2300del (p.Thr767fs)	AXIN2 (T702fs +1 more)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 127944	NM_004655.4(AXIN2):c.2285G>A (p.Ser762Asn)	AXIN2 (S762N +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 136489	NM_004655.4(AXIN2):c.2282C>A (p.Ala761Asp)	AXIN2 (A761D +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
Select item 860933	NM_004655.4(AXIN2):c.2281G>A (p.Ala761Thr)	AXIN2 (A761T +1 more)	Single nucleotide variant (missense variant)	Colorectal cancer +3 more	GUncertain significance
Select item 507601	NM_004655.4(AXIN2):c.2277C>G (p.Leu759=)	AXIN2	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign
Select item 1788865	NM_004655.4(AXIN2):c.2276T>A (p.Leu759His)	AXIN2 (L759H +1 more)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 240012	NM_004655.4(AXIN2):c.2273C>T (p.Ala758Val)	AXIN2 (A758V +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 127943	NM_004655.4(AXIN2):c.2272G>A (p.Ala758Thr)	AXIN2 (A758T +1 more)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 645560	NM_004655.4(AXIN2):c.2264G>T (p.Gly755Val)	AXIN2 (G755V +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 533254	NM_004655.4(AXIN2):c.2262A>C (p.Ala754=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GBenign/Likely benign
Select item 464601	NM_004655.4(AXIN2):c.2249C>T (p.Pro750Leu)	AXIN2 (P750L +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +4 more	GUncertain significance
Select item 652604	NM_004655.4(AXIN2):c.2248C>T (p.Pro750Ser)	AXIN2 (P750S +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 234897	NM_004655.4(AXIN2):c.2240A>G (p.His747Arg)	AXIN2 (H747R +1 more)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 182012	NM_004655.4(AXIN2):c.2239C>T (p.His747Tyr)	AXIN2 (H747Y +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 240011	NM_004655.4(AXIN2):c.2238-7T>C	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome +1 more	GLikely benign
Select item 1158101	NM_004655.4(AXIN2):c.2238-9T>A	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome +1 more	GConflicting classifications of pathogenicity
Select item 381348	NM_004655.4(AXIN2):c.2238-15C>T	AXIN2	Single nucleotide variant (intron variant)	not specified +1 more	GLikely benign
Select item 509104	NM_004655.4(AXIN2):c.2238-18A>G	AXIN2	Single nucleotide variant (intron variant)	not specified +1 more	GLikely benign
Select item 1208707	NM_004655.4(AXIN2):c.2238-292G>A	AXIN2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 679754	NM_004655.4(AXIN2):c.2237+151T>C	AXIN2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 182019	NM_004655.4(AXIN2):c.2237+3G>A	AXIN2	Single nucleotide variant (intron variant)	not provided +3 more	GBenign/Likely benign
Select item 3370962	NM_004655.4(AXIN2):c.2237+2T>C	AXIN2	Single nucleotide variant (splice donor variant)	not provided	GUncertain significance
Select item 658798	NM_004655.4(AXIN2):c.2231C>T (p.Pro744Leu)	AXIN2 (P744L +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 422840	NM_004655.4(AXIN2):c.2218C>T (p.Pro740Ser)	AXIN2 (P740S +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 464600	NM_004655.4(AXIN2):c.2216A>T (p.Asn739Ile)	AXIN2 (N739I +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +2 more	GUncertain significance
Select item 408802	NM_004655.4(AXIN2):c.2216A>G (p.Asn739Ser)	AXIN2 (N739S +1 more)	Single nucleotide variant (missense variant)	AXIN2-related disorder +4 more	GConflicting classifications of pathogenicity
Select item 240010	NM_004655.4(AXIN2):c.2213C>T (p.Ser738Phe)	AXIN2 (S738F +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
Select item 533193	NM_004655.4(AXIN2):c.2206C>A (p.Pro736Thr)	AXIN2 (P736T +1 more)	Single nucleotide variant (missense variant)	Colorectal cancer +4 more	GUncertain significance
Select item 652406	NM_004655.4(AXIN2):c.2204C>T (p.Thr735Ile)	AXIN2 (T670I +1 more)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 240009	NM_004655.4(AXIN2):c.2196G>A (p.Thr732=)	AXIN2	Single nucleotide variant (synonymous variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 234274	NM_004655.4(AXIN2):c.2195C>T (p.Thr732Met)	AXIN2 (T732M +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 240008	NM_004655.4(AXIN2):c.2184C>T (p.Ala728=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome +3 more	GBenign/Likely benign
Select item 464597	NM_004655.4(AXIN2):c.2182G>A (p.Ala728Thr)	AXIN2 (A728T +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +4 more	GUncertain significance
Select item 663154	NM_004655.4(AXIN2):c.2180C>T (p.Ser727Leu)	AXIN2 (S727L +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 422158	NM_004655.4(AXIN2):c.2179T>C (p.Ser727Pro)	AXIN2 (S727P +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 421286	NM_004655.4(AXIN2):c.2174A>G (p.Asn725Ser)	AXIN2 (N725S +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1809813	NM_004655.4(AXIN2):c.2148T>A (p.Cys716Ter)	AXIN2 (C651* +1 more)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 668237	NM_004655.4(AXIN2):c.2142-10G>C	AXIN2	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 1252831	NM_004655.4(AXIN2):c.2142-20C>T	AXIN2	Single nucleotide variant (intron variant)	not provided +2 more	GBenign/Likely benign
Select item 1183260	NM_004655.4(AXIN2):c.2141+263T>C	AXIN2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1247170	NM_004655.4(AXIN2):c.2141+73G>A	AXIN2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 511642	NM_004655.4(AXIN2):c.2141+19T>A	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome +1 more	GLikely benign
Select item 464596	NM_004655.4(AXIN2):c.2141+5G>A	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome +3 more	GUncertain significance
Select item 419353	NM_004655.4(AXIN2):c.2141+4A>G	AXIN2	Single nucleotide variant (intron variant)	AXIN2-related disorder +3 more	GUncertain significance
Select item 422352	NM_004655.4(AXIN2):c.2141G>A (p.Arg714Gln)	AXIN2 (R714Q +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 240007	NM_004655.4(AXIN2):c.2140C>T (p.Arg714Trp)	AXIN2 (R714W +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 415204	NM_004655.4(AXIN2):c.2130C>A (p.Pro710=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
Select item 324644	NM_004655.4(AXIN2):c.2124G>A (p.Ser708=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 220937	NM_004655.4(AXIN2):c.2124G>C (p.Ser708=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
Select item 127942	NM_004655.4(AXIN2):c.2123C>T (p.Ser708Leu)	AXIN2 (S708L +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +4 more	GUncertain significance
Select item 1093127	NM_004655.4(AXIN2):c.2121G>A (p.Val707=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 391659	NM_004655.4(AXIN2):c.2112A>T (p.Leu704=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome +1 more	GBenign/Likely benign
Select item 136488	NM_004655.4(AXIN2):c.2109G>A (p.Arg703=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome +3 more	GBenign
Select item 378997	NM_004655.4(AXIN2):c.2103T>C (p.Cys701=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GBenign/Likely benign
Select item 422982	NM_004655.4(AXIN2):c.2102G>T (p.Cys701Phe)	AXIN2 (C701F +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 386532	NM_004655.4(AXIN2):c.2100C>T (p.Ala700=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 942233	NM_004655.4(AXIN2):c.2087A>G (p.Gln696Arg)	AXIN2 (Q631R +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +2 more	GUncertain significance
Select item 415218	NM_004655.4(AXIN2):c.2083G>T (p.Ala695Ser)	AXIN2 (A695S +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 388544	NM_004655.4(AXIN2):c.2079G>A (p.Thr693=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
Select item 464593	NM_004655.4(AXIN2):c.2068C>T (p.Pro690Ser)	AXIN2 (P690S +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +2 more	GUncertain significance
Select item 581811	NM_004655.4(AXIN2):c.2066C>G (p.Thr689Ser)	AXIN2 (T689S +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 393100	NM_004655.4(AXIN2):c.2064G>A (p.Leu688=)	AXIN2	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign

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