"Quest Diagnostics Nichols Institute San Juan Capistrano"[submitter] A - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 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 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 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 408798	NM_004655.4(AXIN2):c.2366G>C (p.Gly789Ala)	AXIN2 (G789A +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +2 more	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 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 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 182019	NM_004655.4(AXIN2):c.2237+3G>A	AXIN2	Single nucleotide variant (intron variant)	not provided +3 more	GBenign/Likely benign
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 570274	NM_004655.4(AXIN2):c.2206C>T (p.Pro736Ser)	AXIN2 (P736S +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +2 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 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 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 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 408771	NM_004655.4(AXIN2):c.2102G>C (p.Cys701Ser)	AXIN2 (C701S +1 more)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
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 136487	NM_004655.4(AXIN2):c.2052G>A (p.Ala684=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome +3 more	GBenign/Likely benign
Select item 1477134	NM_004655.4(AXIN2):c.2048C>G (p.Pro683Arg)	AXIN2 (P618R +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 182018	NM_004655.4(AXIN2):c.2013_2024del (p.Thr672_Arg675del)	AXIN2	Deletion (inframe_deletion)	not provided +3 more	GBenign
Select item 533157	NM_004655.4(AXIN2):c.2021C>T (p.Pro674Leu)	AXIN2 (P674L +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +3 more	GConflicting classifications of pathogenicity
Select item 240006	NM_004655.4(AXIN2):c.2012G>C (p.Arg671Pro)	AXIN2 (R671P +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +2 more	GConflicting classifications of pathogenicity
Select item 240005	NM_004655.4(AXIN2):c.2004G>A (p.Gly668=)	AXIN2	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 234452	NM_004655.4(AXIN2):c.1987T>C (p.Trp663Arg)	AXIN2 (W663R +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 127939	NM_004655.4(AXIN2):c.1985T>C (p.Leu662Pro)	AXIN2 (L662P +1 more)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 240002	NM_004655.4(AXIN2):c.1975C>T (p.Arg659Trp)	AXIN2 (R659W +1 more)	Single nucleotide variant (missense variant)	Colorectal cancer +4 more	GLikely benign
Select item 240001	NM_004655.4(AXIN2):c.1962C>A (p.Gly654=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
Select item 1330108	NM_004655.4(AXIN2):c.1954T>C (p.Ser652Pro)	AXIN2 (S587P +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +3 more	GUncertain significance
Select item 408813	NM_004655.4(AXIN2):c.1916G>A (p.Ser639Asn)	AXIN2 (S639N +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +3 more	GUncertain significance
Select item 533167	NM_004655.4(AXIN2):c.1908-2A>G	AXIN2	Single nucleotide variant (splice acceptor variant)	Colorectal cancer +3 more	GConflicting classifications of pathogenicity
Select item 234541	NM_004655.4(AXIN2):c.1904A>G (p.His635Arg)	AXIN2 (H635R)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GUncertain significance
Select item 182008	NM_004655.4(AXIN2):c.1882C>T (p.Arg628Trp)	AXIN2 (R628W)	Single nucleotide variant (missense variant +1 more)	Oligodontia-cancer predisposition syndrome +3 more	GConflicting classifications of pathogenicity
Select item 240000	NM_004655.4(AXIN2):c.1829G>A (p.Arg610Gln)	AXIN2 (R610Q)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 136486	NM_004655.4(AXIN2):c.1807G>C (p.Ala603Pro)	AXIN2 (A603P)	Single nucleotide variant (missense variant +1 more)	not specified +4 more	GBenign/Likely benign
Select item 388466	NM_004655.4(AXIN2):c.1758G>A (p.Thr586=)	AXIN2	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GBenign/Likely benign
Select item 127937	NM_004655.4(AXIN2):c.1685C>T (p.Pro562Leu)	AXIN2 (P562L)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 415206	NM_004655.4(AXIN2):c.1635G>A (p.Gly545=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 567639	NM_004655.4(AXIN2):c.1618C>A (p.His540Asn)	AXIN2 (H540N)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 136484	NM_004655.4(AXIN2):c.1615G>A (p.Val539Met)	AXIN2 (V539M)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +4 more	GBenign/Likely benign
Select item 408803	NM_004655.4(AXIN2):c.1598C>T (p.Ala533Val)	AXIN2 (A533V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 1015418	NM_004655.4(AXIN2):c.1593C>G (p.Ile531Met)	AXIN2 (I531M)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +2 more	GConflicting classifications of pathogenicity
Select item 408782	NM_004655.4(AXIN2):c.1586A>G (p.Glu529Gly)	AXIN2 (E529G)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +2 more	GUncertain significance
Select item 239991	NM_004655.4(AXIN2):c.1583A>G (p.Lys528Arg)	AXIN2 (K528R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 464557	NM_004655.4(AXIN2):c.1582A>G (p.Lys528Glu)	AXIN2 (K528E)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +4 more	GUncertain significance
Select item 136483	NM_004655.4(AXIN2):c.1573C>G (p.Pro525Ala)	AXIN2 (P525A)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +3 more	GBenign
Select item 127936	NM_004655.4(AXIN2):c.1557C>G (p.Ile519Met)	AXIN2 (I519M)	Single nucleotide variant (missense variant)	Colorectal cancer +4 more	GUncertain significance
Select item 136482	NM_004655.4(AXIN2):c.1545C>T (p.His515=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome +3 more	GBenign/Likely benign
Select item 324645	NM_004655.4(AXIN2):c.1532C>T (p.Thr511Met)	AXIN2 (T511M)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 136481	NM_004655.4(AXIN2):c.1530G>A (p.Thr510=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome +3 more	GBenign/Likely benign
Select item 863030	NM_004655.4(AXIN2):c.1529C>T (p.Thr510Met)	AXIN2 (T510M)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +2 more	GUncertain significance
Select item 408808	NM_004655.4(AXIN2):c.1485C>T (p.Gly495=)	AXIN2	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 182004	NM_004655.4(AXIN2):c.1481C>T (p.Pro494Leu)	AXIN2 (P494L)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 1999221	NM_004655.4(AXIN2):c.1479G>T (p.Ser493=)	AXIN2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 239989	NM_004655.4(AXIN2):c.1478C>G (p.Ser493Trp)	AXIN2 (S493W)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +3 more	GUncertain significance
Select item 408807	NM_004655.4(AXIN2):c.1470G>A (p.Ala490=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GBenign/Likely benign
Select item 2682047	NM_004655.4(AXIN2):c.1426C>T (p.Gln476Ter)	AXIN2 (Q476*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 234272	NM_004655.4(AXIN2):c.1404CCA[7] (p.His474dup)	AXIN2	Microsatellite (inframe_insertion)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 533170	NM_004655.4(AXIN2):c.1400C>T (p.Pro467Leu)	AXIN2 (P467L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 745226	NM_004655.4(AXIN2):c.1398C>G (p.Ser466=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GBenign/Likely benign
Select item 239984	NM_004655.4(AXIN2):c.1383C>T (p.Ser461=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome +4 more	GBenign/Likely benign
Select item 415213	NM_004655.4(AXIN2):c.1380T>C (p.Tyr460=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
Select item 182002	NM_004655.4(AXIN2):c.1376G>A (p.Arg459His)	AXIN2 (R459H)	Single nucleotide variant (missense variant)	AXIN2-related disorder +3 more	GConflicting classifications of pathogenicity
Select item 415211	NM_004655.4(AXIN2):c.1368C>T (p.Gly456=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GBenign/Likely benign
Select item 239983	NM_004655.4(AXIN2):c.1338C>A (p.Val446=)	AXIN2	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 377545	NM_004655.4(AXIN2):c.1327C>T (p.Leu443=)	AXIN2	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 136479	NM_004655.4(AXIN2):c.1305G>A (p.Pro435=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome +3 more	GBenign/Likely benign
Select item 464531	NM_004655.4(AXIN2):c.1273C>T (p.Leu425=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome +2 more	GBenign/Likely benign
Select item 1135621	NM_004655.4(AXIN2):c.1272C>G (p.Ser424=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GBenign/Likely benign
Select item 565679	NM_004655.4(AXIN2):c.1261C>T (p.His421Tyr)	AXIN2 (H421Y)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 136478	NM_004655.4(AXIN2):c.1250C>T (p.Ala417Val)	AXIN2 (A417V)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +3 more	GBenign/Likely benign
Select item 136477	NM_004655.4(AXIN2):c.1235A>G (p.Asn412Ser)	AXIN2 (N412S)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +4 more	GBenign/Likely benign
Select item 408784	NM_004655.4(AXIN2):c.1222G>A (p.Glu408Lys)	AXIN2 (E408K)	Single nucleotide variant (missense variant)	Colorectal cancer +3 more	GConflicting classifications of pathogenicity
Select item 234485	NM_004655.4(AXIN2):c.1181G>A (p.Arg394His)	AXIN2 (R394H)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
Select item 408832	NM_004655.4(AXIN2):c.1180C>T (p.Arg394Cys)	AXIN2 (R394C)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +3 more	GUncertain significance
Select item 415200	NM_004655.4(AXIN2):c.1176G>A (p.Glu392=)	AXIN2	Single nucleotide variant (synonymous variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 516710	NM_004655.4(AXIN2):c.1171C>T (p.Leu391=)	AXIN2	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 127934	NM_004655.4(AXIN2):c.1168A>G (p.Ser390Gly)	AXIN2 (S390G)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 136476	NM_004655.4(AXIN2):c.1101C>T (p.Pro367=)	AXIN2	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 239975	NM_004655.4(AXIN2):c.1089C>A (p.Thr363=)	AXIN2	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign
Select item 415246	NM_004655.4(AXIN2):c.1083G>A (p.Glu361=)	AXIN2	Single nucleotide variant (synonymous variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 182001	NM_004655.4(AXIN2):c.1070G>A (p.Arg357His)	AXIN2 (R357H)	Single nucleotide variant (missense variant)	not specified +4 more	GBenign/Likely benign
Select item 533211	NM_004655.4(AXIN2):c.1069C>T (p.Arg357Cys)	AXIN2 (R357C)	Single nucleotide variant (missense variant)	Colorectal cancer +3 more	GUncertain significance
Select item 136475	NM_004655.4(AXIN2):c.1059+8C>T	AXIN2	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
Select item 2682037	NM_004655.4(AXIN2):c.1019G>T (p.Ser340Ile)	AXIN2 (S340I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1716948	NM_004655.4(AXIN2):c.1013A>T (p.His338Leu)	AXIN2 (H338L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 408821	NM_004655.4(AXIN2):c.976C>T (p.Arg326Cys)	AXIN2 (R326C)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 570059	NM_004655.4(AXIN2):c.971C>T (p.Pro324Leu)	AXIN2 (P324L)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 408794	NM_004655.4(AXIN2):c.958G>C (p.Asp320His)	AXIN2 (D320H)	Single nucleotide variant (missense variant)	Colorectal cancer +4 more	GUncertain significance
Select item 464651	NM_004655.4(AXIN2):c.955G>A (p.Val319Ile)	AXIN2 (V319I)	Single nucleotide variant (missense variant)	Colorectal cancer +3 more	GUncertain significance
Select item 464649	NM_004655.4(AXIN2):c.942G>T (p.Met314Ile)	AXIN2 (M314I)	Single nucleotide variant (missense variant)	Colorectal cancer +3 more	GUncertain significance
Select item 464648	NM_004655.4(AXIN2):c.934A>G (p.Met312Val)	AXIN2 (M312V)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +2 more	GUncertain significance
Select item 240038	NM_004655.4(AXIN2):c.879A>G (p.Pro293=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
Select item 2095863	NM_004655.4(AXIN2):c.832G>C (p.Asp278His)	AXIN2 (D278H)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +1 more	GUncertain significance
Select item 1632519	NM_004655.4(AXIN2):c.822C>T (p.Phe274=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome +2 more	GConflicting classifications of pathogenicity
Select item 240034	NM_004655.4(AXIN2):c.815+7C>T	AXIN2	Single nucleotide variant (intron variant)	not provided +2 more	GBenign/Likely benign
Select item 240033	NM_004655.4(AXIN2):c.815+3dup	AXIN2	Duplication (intron variant)	not provided +2 more	GLikely benign
Select item 1052720	NM_004655.4(AXIN2):c.739G>C (p.Val247Leu)	AXIN2 (V247L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity

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