C1837750[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar - NCBI

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

Search results

Items: 1 to 100 of 265

<< First< Prev

Page of 3

	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)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 641425	NM_004655.4(AXIN2):c.2501G>A (p.Arg834Gln)	AXIN2 (R769Q +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +2 more	GUncertain significance
Select item 821330	NM_004655.4(AXIN2):c.2479G>A (p.Val827Met)	AXIN2 (V762M +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +2 more	GUncertain significance
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 1972070	NM_004655.4(AXIN2):c.2462T>C (p.Ile821Thr)	AXIN2 (I756T +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +1 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 837820	NM_004655.4(AXIN2):c.2437G>A (p.Ala813Thr)	AXIN2 (A748T +1 more)	Single nucleotide variant (missense variant)	Colorectal cancer +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)	Oligodontia-cancer predisposition syndrome +2 more	GUncertain significance
Select item 639684	NM_004655.4(AXIN2):c.2405+5G>A	AXIN2	Single nucleotide variant (intron variant)	Colorectal cancer +1 more	GUncertain significance
Select item 1046893	NM_004655.4(AXIN2):c.2383C>G (p.Leu795Val)	AXIN2 (L795V +1 more)	Single nucleotide variant (missense variant)	Colorectal cancer +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 648156	NM_004655.4(AXIN2):c.2302T>C (p.Tyr768His)	AXIN2 (Y703H +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
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 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 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 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 1788195	NM_004655.4(AXIN2):c.2236G>T (p.Asp746Tyr)	AXIN2 (D746Y +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +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)	Oligodontia-cancer predisposition syndrome +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)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 576269	NM_004655.4(AXIN2):c.2219C>G (p.Pro740Arg)	AXIN2 (P740R +1 more)	Single nucleotide variant (missense variant)	Colorectal cancer +3 more	GUncertain significance
Select item 533186	NM_004655.4(AXIN2):c.2207C>T (p.Pro736Leu)	AXIN2 (P736L +1 more)	Single nucleotide variant (missense variant)	Colorectal cancer +2 more	GUncertain significance
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 533156	NM_004655.4(AXIN2):c.2170A>G (p.Arg724Gly)	AXIN2 (R724G +1 more)	Single nucleotide variant (missense variant)	Colorectal cancer +2 more	GUncertain significance
Select item 841462	NM_004655.4(AXIN2):c.2137C>T (p.Gln713Ter)	AXIN2 (Q648* +1 more)	Single nucleotide variant (nonsense)	Colorectal cancer +2 more	GPathogenic/Likely pathogenic
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 663214	NM_004655.4(AXIN2):c.2117A>G (p.Glu706Gly)	AXIN2 (E641G +1 more)	Single nucleotide variant (missense variant)	Colorectal cancer +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)	not provided +3 more	GUncertain significance
Select item 854399	NM_004655.4(AXIN2):c.2065A>G (p.Thr689Ala)	AXIN2 (T689A +1 more)	Single nucleotide variant (missense variant)	Colorectal cancer +1 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)	Hereditary cancer-predisposing syndrome +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)	Colorectal cancer +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)	not provided +3 more	GUncertain significance
Select item 1040615	NM_004655.4(AXIN2):c.2029C>T (p.His677Tyr)	AXIN2 (H612Y +1 more)	Single nucleotide variant (missense variant)	Colorectal cancer +2 more	GUncertain significance
Select item 533234	NM_004655.4(AXIN2):c.2024G>T (p.Arg675Leu)	AXIN2 (R675L +1 more)	Single nucleotide variant (missense variant)	Colorectal cancer +2 more	GUncertain significance
Select item 182011	NM_004655.4(AXIN2):c.2024G>A (p.Arg675His)	AXIN2 (R675H +1 more)	Single nucleotide variant (missense variant)	not provided +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 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 533222	NM_004655.4(AXIN2):c.1982_2008del (p.His661_His669del)	AXIN2	Deletion (inframe_deletion)	Colorectal cancer +2 more	GUncertain significance
Select item 420080	NM_004655.4(AXIN2):c.2002G>A (p.Gly668Arg)	AXIN2 (G668R +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing 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 545741	NM_004655.4(AXIN2):c.1994dup (p.Asn666fs)	AXIN2 (N601fs +1 more)	Duplication (frameshift variant)	Oligodontia-cancer predisposition syndrome +3 more	GPathogenic
Select item 5880	NM_004655.4(AXIN2):c.1994del (p.Gly665fs)	AXIN2 (G665fs +1 more)	Deletion (frameshift variant)	Colorectal cancer +2 more	GPathogenic/Likely pathogenic
Select item 408850	NM_004655.4(AXIN2):c.1987T>G (p.Trp663Gly)	AXIN2 (W663G +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +4 more	GConflicting classifications of pathogenicity
Select item 464588	NM_004655.4(AXIN2):c.1984C>G (p.Leu662Val)	AXIN2 (L662V +1 more)	Single nucleotide variant (missense variant)	Colorectal cancer +3 more	GUncertain significance
Select item 182010	NM_004655.4(AXIN2):c.1976G>A (p.Arg659Gln)	AXIN2 (R659Q +1 more)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 566169	NM_004655.4(AXIN2):c.1974C>G (p.Ser658Arg)	AXIN2 (S658R +1 more)	Single nucleotide variant (missense variant)	Colorectal cancer +2 more	GConflicting classifications of pathogenicity
Select item 943579	NM_004655.4(AXIN2):c.1969G>A (p.Ala657Thr)	AXIN2 (A657T +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +3 more	GUncertain significance
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 2746814	NM_004655.4(AXIN2):c.1960G>A (p.Gly654Ser)	AXIN2 (G654S +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +1 more	GUncertain significance
Select item 464586	NM_004655.4(AXIN2):c.1952C>G (p.Ser651Trp)	AXIN2 (S651W +1 more)	Single nucleotide variant (missense variant)	Colorectal cancer +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)	Oligodontia-cancer predisposition 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)	Hereditary cancer-predisposing syndrome +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)	Hereditary cancer-predisposing syndrome +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)	Oligodontia-cancer predisposition syndrome +4 more	GUncertain significance
Select item 863891	NM_004655.4(AXIN2):c.1919C>T (p.Thr640Ile)	AXIN2 (T575I +1 more)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +2 more	GConflicting classifications of pathogenicity
Select item 408851	NM_004655.4(AXIN2):c.1918A>C (p.Thr640Pro)	AXIN2 (T640P +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 464582	NM_004655.4(AXIN2):c.1908-1G>A	AXIN2	Single nucleotide variant (splice acceptor variant)	not provided +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)	not provided +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)	Colorectal cancer +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)	Colorectal cancer +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)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 1490447	NM_004655.4(AXIN2):c.1849C>T (p.Gln617Ter)	AXIN2 (Q617*)	Single nucleotide variant (nonsense +1 more)	Colorectal cancer +1 more	GUncertain significance
Select item 579452	NM_004655.4(AXIN2):c.1828C>T (p.Arg610Trp)	AXIN2 (R610W)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +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 1037840	NM_004655.4(AXIN2):c.1821G>C (p.Gln607His)	AXIN2 (Q607H)	Single nucleotide variant (missense variant +1 more)	Colorectal cancer +2 more	GUncertain significance
Select item 2067600	NM_004655.4(AXIN2):c.1799C>T (p.Pro600Leu)	AXIN2 (P600L)	Single nucleotide variant (missense variant +1 more)	Oligodontia-cancer predisposition syndrome +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 533176	NM_004655.4(AXIN2):c.1783A>G (p.Arg595Gly)	AXIN2 (R595G)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 234273	NM_004655.4(AXIN2):c.1780G>A (p.Ala594Thr)	AXIN2 (A594T)	Single nucleotide variant (missense variant +1 more)	Colorectal cancer +3 more	GConflicting classifications of pathogenicity
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 1779808	NM_004655.4(AXIN2):c.1771G>A (p.Ala591Thr)	AXIN2 (A591T)	Single nucleotide variant (missense variant +1 more)	Colorectal cancer +2 more	GUncertain significance
Select item 955235	NM_004655.4(AXIN2):c.1769T>A (p.Leu590Gln)	AXIN2 (L590Q)	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)	Oligodontia-cancer predisposition syndrome +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 1433468	NM_004655.4(AXIN2):c.1751A>C (p.Lys584Thr)	AXIN2 (K584T)	Single nucleotide variant (missense variant +1 more)	Oligodontia-cancer predisposition syndrome +2 more	GUncertain significance
Select item 408773	NM_004655.4(AXIN2):c.1747G>A (p.Gly583Arg)	AXIN2 (G583R)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GUncertain significance
Select item 239998	NM_004655.4(AXIN2):c.1744A>C (p.Asn582His)	AXIN2 (N582H)	Single nucleotide variant (missense variant +1 more)	Colorectal cancer +2 more	GConflicting classifications of pathogenicity
Select item 580356	NM_004655.4(AXIN2):c.1739A>G (p.Lys580Arg)	AXIN2 (K580R)	Single nucleotide variant (missense variant +1 more)	Colorectal cancer +2 more	GUncertain significance
Select item 1063773	NM_004655.4(AXIN2):c.1730C>A (p.Thr577Asn)	AXIN2 (T577N)	Single nucleotide variant (missense variant +1 more)	Colorectal cancer +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)	Colorectal cancer +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)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 239996	NM_004655.4(AXIN2):c.1708T>G (p.Phe570Val)	AXIN2 (F570V)	Single nucleotide variant (missense variant)	Colorectal cancer +4 more	GUncertain significance
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 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)	not provided +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)	not provided +3 more	GUncertain significance
Select item 239995	NM_004655.4(AXIN2):c.1633G>T (p.Gly545Trp)	AXIN2 (G545W)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 408799	NM_004655.4(AXIN2):c.1631C>T (p.Pro544Leu)	AXIN2 (P544L)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +3 more	GConflicting classifications of pathogenicity
Select item 861853	NM_004655.4(AXIN2):c.1630C>T (p.Pro544Ser)	AXIN2 (P544S)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 845420	NM_004655.4(AXIN2):c.1624T>C (p.Phe542Leu)	AXIN2 (F542L)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +2 more	GUncertain significance
Select item 1064234	NM_004655.4(AXIN2):c.1620C>G (p.His540Gln)	AXIN2 (H540Q)	Single nucleotide variant (missense variant)	Colorectal cancer +2 more	GUncertain significance
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 239993	NM_004655.4(AXIN2):c.1612C>T (p.Arg538Trp)	AXIN2 (R538W)	Single nucleotide variant (missense variant)	Colorectal cancer +3 more	GUncertain significance

<< First< Prev

Page of 3