"Baylor Genetics"[submitter] AND "AXIN2"[gene] - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 1 to 100 of 192

<< First< Prev

Page of 2

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 127946	NM_004655.4(AXIN2):c.2521C>T (p.Arg841Trp)	AXIN2 (R841W +1 more)	Single nucleotide variant (missense variant)	Colorectal cancer +4 more	GUncertain significance
Select item 641425	NM_004655.4(AXIN2):c.2501G>A (p.Arg834Gln)	AXIN2 (R769Q +1 more)	Single nucleotide variant (missense variant)	Colorectal cancer +2 more	GUncertain significance
Select item 2679874	NM_004655.4(AXIN2):c.2489T>G (p.Met830Arg)	AXIN2 (M765R +1 more)	Single nucleotide variant (missense variant)	Colorectal cancer	GUncertain significance
Select item 837820	NM_004655.4(AXIN2):c.2437G>A (p.Ala813Thr)	AXIN2 (A748T +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +2 more	GUncertain significance
Select item 1791103	NM_004655.4(AXIN2):c.2427C>A (p.Ser809Arg)	AXIN2 (S809R +1 more)	Single nucleotide variant (missense variant)	Colorectal cancer +2 more	GUncertain significance
Select item 1046893	NM_004655.4(AXIN2):c.2383C>G (p.Leu795Val)	AXIN2 (L795V +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +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 +4 more	GConflicting classifications of pathogenicity
Select item 648156	NM_004655.4(AXIN2):c.2302T>C (p.Tyr768His)	AXIN2 (Y703H +1 more)	Single nucleotide variant (missense variant)	Colorectal cancer +2 more	GUncertain significance
Select item 464601	NM_004655.4(AXIN2):c.2249C>T (p.Pro750Leu)	AXIN2 (P750L +1 more)	Single nucleotide variant (missense variant)	not specified +4 more	GUncertain significance
Select item 234897	NM_004655.4(AXIN2):c.2240A>G (p.His747Arg)	AXIN2 (H747R +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +3 more	GUncertain significance
Select item 1788195	NM_004655.4(AXIN2):c.2236G>T (p.Asp746Tyr)	AXIN2 (D746Y +1 more)	Single nucleotide variant (missense variant)	Colorectal cancer +2 more	GUncertain significance
Select item 960882	NM_004655.4(AXIN2):c.2223C>G (p.Ser741Arg)	AXIN2 (S676R +1 more)	Single nucleotide variant (missense variant)	Colorectal cancer +1 more	GUncertain significance
Select item 408795	NM_004655.4(AXIN2):c.2222G>A (p.Ser741Asn)	AXIN2 (S741N +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +2 more	GConflicting classifications of pathogenicity
Select item 533193	NM_004655.4(AXIN2):c.2206C>A (p.Pro736Thr)	AXIN2 (P736T +1 more)	Single nucleotide variant (missense variant)	not specified +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)	Oligodontia-cancer predisposition syndrome +3 more	GUncertain significance
Select item 2679891	NM_004655.4(AXIN2):c.2172del (p.Asn725fs)	AXIN2 (N660fs +1 more)	Deletion (frameshift variant)	Colorectal cancer	GLikely pathogenic
Select item 841462	NM_004655.4(AXIN2):c.2137C>T (p.Gln713Ter)	AXIN2 (Q648* +1 more)	Single nucleotide variant (nonsense)	Hereditary cancer-predisposing syndrome +2 more	GPathogenic/Likely pathogenic
Select item 663214	NM_004655.4(AXIN2):c.2117A>G (p.Glu706Gly)	AXIN2 (E641G +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 408771	NM_004655.4(AXIN2):c.2102G>C (p.Cys701Ser)	AXIN2 (C701S +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +3 more	GUncertain significance
Select item 574566	NM_004655.4(AXIN2):c.2060C>T (p.Pro687Leu)	AXIN2 (P687L +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 1036060	NM_004655.4(AXIN2):c.2050G>A (p.Ala684Thr)	AXIN2 (A619T +1 more)	Single nucleotide variant (missense variant)	Colorectal cancer +2 more	GUncertain significance
Select item 533214	NM_004655.4(AXIN2):c.2048C>T (p.Pro683Leu)	AXIN2 (P683L +1 more)	Single nucleotide variant (missense variant)	not specified +3 more	GUncertain significance
Select item 653576	NM_004655.4(AXIN2):c.2047C>G (p.Pro683Ala)	AXIN2 (P618A +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +3 more	GUncertain significance
Select item 533234	NM_004655.4(AXIN2):c.2024G>T (p.Arg675Leu)	AXIN2 (R675L +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +2 more	GUncertain significance
Select item 240006	NM_004655.4(AXIN2):c.2012G>C (p.Arg671Pro)	AXIN2 (R671P +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 408768	NM_004655.4(AXIN2):c.2011C>T (p.Arg671Cys)	AXIN2 (R671C +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 420080	NM_004655.4(AXIN2):c.2002G>A (p.Gly668Arg)	AXIN2 (G668R +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +3 more	GUncertain significance
Select item 240004	NM_004655.4(AXIN2):c.2000G>A (p.Ser667Asn)	AXIN2 (S667N +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +4 more	GUncertain significance
Select item 5880	NM_004655.4(AXIN2):c.1994del (p.Gly665fs)	AXIN2 (G665fs +1 more)	Deletion (frameshift variant)	Hereditary cancer-predisposing syndrome +2 more	GPathogenic/Likely pathogenic
Select item 464588	NM_004655.4(AXIN2):c.1984C>G (p.Leu662Val)	AXIN2 (L662V +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 566169	NM_004655.4(AXIN2):c.1974C>G (p.Ser658Arg)	AXIN2 (S658R +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +2 more	GConflicting classifications of pathogenicity
Select item 533239	NM_004655.4(AXIN2):c.1967G>A (p.Arg656Gln)	AXIN2 (R656Q +1 more)	Single nucleotide variant (missense variant)	Colorectal cancer +2 more	GUncertain significance
Select item 464586	NM_004655.4(AXIN2):c.1952C>G (p.Ser651Trp)	AXIN2 (S651W +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 182009	NM_004655.4(AXIN2):c.1948C>T (p.Arg650Cys)	AXIN2 (R650C +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 182022	NM_004655.4(AXIN2):c.1934C>T (p.Pro645Leu)	AXIN2 (P645L +1 more)	Single nucleotide variant (missense variant)	Colorectal cancer +3 more	GUncertain significance
Select item 854457	NM_004655.4(AXIN2):c.1933C>T (p.Pro645Ser)	AXIN2 (P580S +1 more)	Single nucleotide variant (missense variant)	Colorectal cancer +3 more	GConflicting classifications of pathogenicity
Select item 408817	NM_004655.4(AXIN2):c.1931A>G (p.Tyr644Cys)	AXIN2 (Y644C +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +4 more	GUncertain significance
Select item 408851	NM_004655.4(AXIN2):c.1918A>C (p.Thr640Pro)	AXIN2 (T640P +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing 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 408815	NM_004655.4(AXIN2):c.1906A>G (p.Ser636Gly)	AXIN2 (S636G)	Single nucleotide variant (missense variant +1 more)	Oligodontia-cancer predisposition syndrome +3 more	GUncertain significance
Select item 234541	NM_004655.4(AXIN2):c.1904A>G (p.His635Arg)	AXIN2 (H635R)	Single nucleotide variant (missense variant +1 more)	Oligodontia-cancer predisposition syndrome +3 more	GUncertain significance
Select item 1921896	NM_004655.4(AXIN2):c.1894C>T (p.Pro632Ser)	AXIN2 (P632S)	Single nucleotide variant (missense variant +1 more)	Oligodontia-cancer predisposition syndrome +2 more	GUncertain significance
Select item 954363	NM_004655.4(AXIN2):c.1883G>A (p.Arg628Gln)	AXIN2 (R628Q)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 533225	NM_004655.4(AXIN2):c.1878T>A (p.Ser626Arg)	AXIN2 (S626R)	Single nucleotide variant (missense variant +1 more)	Oligodontia-cancer predisposition syndrome +2 more	GUncertain significance
Select item 1396722	NM_004655.4(AXIN2):c.1874A>C (p.Glu625Ala)	AXIN2 (E625A)	Single nucleotide variant (missense variant +1 more)	Colorectal cancer +2 more	GUncertain significance
Select item 579452	NM_004655.4(AXIN2):c.1828C>T (p.Arg610Trp)	AXIN2 (R610W)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GUncertain significance
Select item 639845	NM_004655.4(AXIN2):c.1825C>T (p.Pro609Ser)	AXIN2 (P609S)	Single nucleotide variant (missense variant +1 more)	Colorectal cancer +2 more	GUncertain significance
Select item 1408220	NM_004655.4(AXIN2):c.1795G>T (p.Ala599Ser)	AXIN2 (A599S)	Single nucleotide variant (missense variant +1 more)	Oligodontia-cancer predisposition syndrome +1 more	GUncertain significance
Select item 1697644	NM_004655.4(AXIN2):c.1786G>A (p.Glu596Lys)	AXIN2 (E596K)	Single nucleotide variant (missense variant +1 more)	Colorectal cancer +2 more	GUncertain significance
Select item 533176	NM_004655.4(AXIN2):c.1783A>G (p.Arg595Gly)	AXIN2 (R595G)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GUncertain significance
Select item 1048974	NM_004655.4(AXIN2):c.1772C>T (p.Ala591Val)	AXIN2 (A591V)	Single nucleotide variant (missense variant +1 more)	Colorectal cancer +2 more	GUncertain significance
Select item 861396	NM_004655.4(AXIN2):c.1763C>T (p.Pro588Leu)	AXIN2 (P588L)	Single nucleotide variant (missense variant +1 more)	Colorectal cancer +2 more	GUncertain significance
Select item 851970	NM_004655.4(AXIN2):c.1759G>A (p.Glu587Lys)	AXIN2 (E587K)	Single nucleotide variant (missense variant +1 more)	Oligodontia-cancer predisposition syndrome +1 more	GUncertain significance
Select item 408773	NM_004655.4(AXIN2):c.1747G>A (p.Gly583Arg)	AXIN2 (G583R)	Single nucleotide variant (missense variant +1 more)	Oligodontia-cancer predisposition syndrome +3 more	GUncertain significance
Select item 1063773	NM_004655.4(AXIN2):c.1730C>A (p.Thr577Asn)	AXIN2 (T577N)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 420377	NM_004655.4(AXIN2):c.1714G>A (p.Gly572Ser)	AXIN2 (G572S)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 1778510	NM_004655.4(AXIN2):c.1709T>C (p.Phe570Ser)	AXIN2 (F570S)	Single nucleotide variant (missense variant)	Colorectal cancer +2 more	GUncertain significance
Select item 239996	NM_004655.4(AXIN2):c.1708T>G (p.Phe570Val)	AXIN2 (F570V)	Single nucleotide variant (missense variant)	Carcinoma of colon +4 more	GUncertain significance
Select item 127937	NM_004655.4(AXIN2):c.1685C>T (p.Pro562Leu)	AXIN2 (P562L)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 408762	NM_004655.4(AXIN2):c.1676C>G (p.Ser559Cys)	AXIN2 (S559C)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 182006	NM_004655.4(AXIN2):c.1651T>C (p.Cys551Arg)	AXIN2 (C551R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +5 more	GUncertain significance
Select item 2471381	NM_004655.4(AXIN2):c.1634G>C (p.Gly545Ala)	AXIN2 (G545A)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 408814	NM_004655.4(AXIN2):c.1633G>A (p.Gly545Arg)	AXIN2 (G545R)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +3 more	GUncertain significance
Select item 239995	NM_004655.4(AXIN2):c.1633G>T (p.Gly545Trp)	AXIN2 (G545W)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 1064234	NM_004655.4(AXIN2):c.1620C>G (p.His540Gln)	AXIN2 (H540Q)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 567639	NM_004655.4(AXIN2):c.1618C>A (p.His540Asn)	AXIN2 (H540N)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 2679884	NM_004655.4(AXIN2):c.1601A>G (p.Glu534Gly)	AXIN2 (E534G)	Single nucleotide variant (missense variant)	Colorectal cancer	GUncertain significance
Select item 1061406	NM_004655.4(AXIN2):c.1594G>A (p.Glu532Lys)	AXIN2 (E532K)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +2 more	GUncertain significance
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 962954	NM_004655.4(AXIN2):c.1555A>C (p.Ile519Leu)	AXIN2 (I519L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 533201	NM_004655.4(AXIN2):c.1555A>G (p.Ile519Val)	AXIN2 (I519V)	Single nucleotide variant (missense variant)	Colorectal cancer +3 more	GUncertain significance
Select item 648472	NM_004655.4(AXIN2):c.1528A>G (p.Thr510Ala)	AXIN2 (T510A)	Single nucleotide variant (missense variant)	Colorectal cancer +1 more	GUncertain significance
Select item 533165	NM_004655.4(AXIN2):c.1516G>A (p.Val506Met)	AXIN2 (V506M)	Single nucleotide variant (missense variant)	Colorectal cancer +2 more	GConflicting classifications of pathogenicity
Select item 408843	NM_004655.4(AXIN2):c.1511G>A (p.Gly504Asp)	AXIN2 (G504D)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +2 more	GUncertain significance
Select item 1723606	NM_004655.4(AXIN2):c.1505G>A (p.Gly502Asp)	AXIN2 (G502D)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 419773	NM_004655.4(AXIN2):c.1504G>T (p.Gly502Cys)	AXIN2 (G502C)	Single nucleotide variant (missense variant)	not specified +4 more	GUncertain significance
Select item 2566119	NM_004655.4(AXIN2):c.1496T>G (p.Leu499Arg)	AXIN2 (L499R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 408836	NM_004655.4(AXIN2):c.1496T>C (p.Leu499Pro)	AXIN2 (L499P)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +2 more	GUncertain significance
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 569428	NM_004655.4(AXIN2):c.1445C>T (p.Pro482Leu)	AXIN2 (P482L)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +3 more	GUncertain significance
Select item 408801	NM_004655.4(AXIN2):c.1436C>A (p.Ser479Tyr)	AXIN2 (S479Y)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 234272	NM_004655.4(AXIN2):c.1404CCA[7] (p.His474dup)	AXIN2	Microsatellite (inframe_insertion)	AXIN2-related condition +4 more	GConflicting classifications of pathogenicity
Select item 408780	NM_004655.4(AXIN2):c.1420C>T (p.His474Tyr)	AXIN2 (H474Y)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +3 more	GUncertain significance
Select item 581265	NM_004655.4(AXIN2):c.1415A>G (p.His472Arg)	AXIN2 (H472R)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +2 more	GConflicting classifications of pathogenicity
Select item 641175	NM_004655.4(AXIN2):c.1411C>T (p.His471Tyr)	AXIN2 (H471Y)	Single nucleotide variant (missense variant)	Colorectal cancer +2 more	GConflicting classifications of pathogenicity
Select item 533170	NM_004655.4(AXIN2):c.1400C>T (p.Pro467Leu)	AXIN2 (P467L)	Single nucleotide variant (missense variant)	Colorectal cancer +3 more	GUncertain significance
Select item 2451653	NM_004655.4(AXIN2):c.1399C>G (p.Pro467Ala)	AXIN2 (P467A)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +2 more	GUncertain significance
Select item 239986	NM_004655.4(AXIN2):c.1394G>A (p.Arg465His)	AXIN2 (R465H)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +3 more	GUncertain significance
Select item 464542	NM_004655.4(AXIN2):c.1384C>T (p.Pro462Ser)	AXIN2 (P462S)	Single nucleotide variant (missense variant)	Colorectal cancer +2 more	GUncertain significance
Select item 533142	NM_004655.4(AXIN2):c.1375C>T (p.Arg459Cys)	AXIN2 (R459C)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +2 more	GUncertain significance
Select item 2679878	NM_004655.4(AXIN2):c.1256C>G (p.Thr419Arg)	AXIN2 (T419R)	Single nucleotide variant (missense variant)	Colorectal cancer	GUncertain significance
Select item 578711	NM_004655.4(AXIN2):c.1238C>T (p.Ser413Leu)	AXIN2 (S413L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 533228	NM_004655.4(AXIN2):c.1229C>T (p.Thr410Ile)	AXIN2 (T410I)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +2 more	GUncertain significance
Select item 408784	NM_004655.4(AXIN2):c.1222G>A (p.Glu408Lys)	AXIN2 (E408K)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +4 more	GConflicting classifications of pathogenicity
Select item 418051	NM_004655.4(AXIN2):c.1207_1209del (p.Glu403del)	AXIN2 (E403del)	Deletion (inframe_deletion)	Colorectal cancer +4 more	GUncertain significance
Select item 533207	NM_004655.4(AXIN2):c.1202A>G (p.Asp401Gly)	AXIN2 (D401G)	Single nucleotide variant (missense variant)	Colorectal cancer +3 more	GUncertain significance
Select item 464525	NM_004655.4(AXIN2):c.1201-2A>G	AXIN2	Single nucleotide variant (splice acceptor variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 834370	NM_004655.4(AXIN2):c.1200+3A>G	AXIN2	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 959158	NM_004655.4(AXIN2):c.1200G>A (p.Glu400=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity

<< First< Prev

Page of 2