ClinVar for Gene (Select 8313) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3335803	NM_004655.4(AXIN2):c.121G>A (p.Gly41Ser)	AXIN2 (G41S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3335792	NM_004655.4(AXIN2):c.1237T>A (p.Ser413Thr)	AXIN2 (S413T)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3335782	NM_004655.4(AXIN2):c.2184C>A (p.Ala728=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3335761	NM_004655.4(AXIN2):c.937T>A (p.Ser313Thr)	AXIN2 (S313T)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3335740	NM_004655.4(AXIN2):c.1405C>A (p.His469Asn)	AXIN2 (H469N)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3335704	NM_004655.4(AXIN2):c.2406-2A>G	AXIN2	Single nucleotide variant (splice acceptor variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3335694	NM_004655.4(AXIN2):c.220C>G (p.Pro74Ala)	AXIN2 (P74A)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3335684	NM_004655.4(AXIN2):c.1692C>T (p.Thr564=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3335674	NM_004655.4(AXIN2):c.2256A>C (p.Lys752Asn)	AXIN2 (K687N +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3335658	NM_004655.4(AXIN2):c.1940A>T (p.Glu647Val)	AXIN2 (E582V +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3335649	NM_004655.4(AXIN2):c.45C>T (p.Ser15=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3335600	NM_004655.4(AXIN2):c.39C>G (p.Pro13=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3335590	NM_004655.4(AXIN2):c.1315C>A (p.Leu439Met)	AXIN2 (L439M)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3335579	NM_004655.4(AXIN2):c.1419C>T (p.His473=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3335569	NM_004655.4(AXIN2):c.2476A>C (p.Thr826Pro)	AXIN2 (T761P +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3335533	NM_004655.4(AXIN2):c.314T>C (p.Val105Ala)	AXIN2 (V105A)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3335511	NM_004655.4(AXIN2):c.444G>C (p.Gln148His)	AXIN2 (Q148H)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3335493	NM_004655.4(AXIN2):c.1226T>A (p.Leu409His)	AXIN2 (L409H)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3335483	NM_004655.4(AXIN2):c.1788A>T (p.Glu596Asp)	AXIN2 (E596D)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3335453	NM_004655.4(AXIN2):c.1090C>A (p.Pro364Thr)	AXIN2 (P364T)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3335425	NM_004655.4(AXIN2):c.953G>C (p.Ser318Thr)	AXIN2 (S318T)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3335413	NM_004655.4(AXIN2):c.1386delinsTCGCCCT (p.Arg463_Ser464insProArg)	AXIN2	Indel (inframe_insertion)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3335403	NM_004655.4(AXIN2):c.1386_1388delinsTCC (p.Arg463Pro)	AXIN2 (R463P)	Indel (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3335084	NM_004655.4(AXIN2):c.2014A>G (p.Thr672Ala)	AXIN2 (T607A +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3335064	NM_004655.4(AXIN2):c.2463C>T (p.Ile821=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3335053	NM_004655.4(AXIN2):c.1466C>T (p.Pro489Leu)	AXIN2 (P489L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3334841	NM_004655.4(AXIN2):c.386G>C (p.Arg129Pro)	AXIN2 (R129P)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3258315	NM_004655.4(AXIN2):c.816G>T (p.Arg272Ser)	AXIN2 (R272S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3258300	NM_004655.4(AXIN2):c.2001C>A (p.Ser667Arg)	AXIN2 (S602R +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3258296	NM_004655.4(AXIN2):c.1965A>T (p.Glu655Asp)	AXIN2 (E655D +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3258292	NM_004655.4(AXIN2):c.1833G>C (p.Glu611Asp)	AXIN2 (E611D)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3258270	NM_004655.4(AXIN2):c.2130C>G (p.Pro710=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3258264	NM_004655.4(AXIN2):c.1599G>C (p.Ala533=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3258257	NM_004655.4(AXIN2):c.815G>A (p.Arg272Lys)	AXIN2 (R272K)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3258249	NM_004655.4(AXIN2):c.82G>A (p.Gly28Arg)	AXIN2 (G28R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3258241	NM_004655.4(AXIN2):c.2087_2108delinsT (p.Gln696_Arg703delinsLeu)	AXIN2	Indel (inframe_indel)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3258211	NM_004655.4(AXIN2):c.2231del (p.Pro744fs)	AXIN2 (P744fs +1 more)	Deletion (frameshift variant)	Hereditary cancer-predisposing syndrome	GPathogenic
Select item 3258200	NM_004655.4(AXIN2):c.1908-12T>G	AXIN2	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3258194	NM_004655.4(AXIN2):c.1470G>T (p.Ala490=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3258170	NM_004655.4(AXIN2):c.358A>G (p.Met120Val)	AXIN2 (M120V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3258159	NM_004655.4(AXIN2):c.1654T>C (p.Tyr552His)	AXIN2 (Y552H)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3258130	NM_004655.4(AXIN2):c.1935C>G (p.Pro645=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3258119	NM_004655.4(AXIN2):c.1262A>T (p.His421Leu)	AXIN2 (H421L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3256219	NM_004655.4(AXIN2):c.1200+46C>T	AXIN2	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3256218	NM_004655.4(AXIN2):c.1200+50C>G	AXIN2	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 3256216	NM_004655.4(AXIN2):c.1201-43C>G	AXIN2	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 3256215	NM_004655.4(AXIN2):c.1712+36G>C	AXIN2	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 3256214	NM_004655.4(AXIN2):c.1713-39C>T	AXIN2	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 3256212	NM_004655.4(AXIN2):c.2237+36G>A	AXIN2	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 3256211	NM_004655.4(AXIN2):c.2238-43T>C	AXIN2	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 3254357	NM_004655.4(AXIN2):c.816-15G>A	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3254356	NM_004655.4(AXIN2):c.18G>A (p.Leu6=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome +1 more	GBenign/Likely benign
Select item 3254354	NM_004655.4(AXIN2):c.957-21_957-20del	AXIN2	Deletion (intron variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3254350	NM_004655.4(AXIN2):c.956+7_956+8del	AXIN2	Deletion (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3254349	NM_004655.4(AXIN2):c.747C>T (p.Gly249=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3254347	NM_004655.4(AXIN2):c.642A>T (p.Gly214=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3254344	NM_004655.4(AXIN2):c.402C>A (p.Ile134=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3254343	NM_004655.4(AXIN2):c.385C>A (p.Arg129=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3254340	NM_004655.4(AXIN2):c.783G>C (p.Val261=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3254334	NM_004655.4(AXIN2):c.315G>A (p.Val105=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3254327	NM_004655.4(AXIN2):c.690A>G (p.Glu230=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3254324	NM_004655.4(AXIN2):c.816-4A>T	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3254320	NM_004655.4(AXIN2):c.399G>T (p.Ala133=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3254319	NM_004655.4(AXIN2):c.957-20T>C	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3254318	NM_004655.4(AXIN2):c.192G>A (p.Glu64=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3254316	NM_004655.4(AXIN2):c.956+10C>T	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3254313	NM_004655.4(AXIN2):c.429_432delinsTATC (p.Ser143_Ile144=)	AXIN2	Indel (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3254311	NM_004655.4(AXIN2):c.816-19T>C	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3254310	NM_004655.4(AXIN2):c.956+9C>A	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3254309	NM_004655.4(AXIN2):c.639G>A (p.Gly213=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3254308	NM_004655.4(AXIN2):c.996G>A (p.Gln332=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3254307	NM_004655.4(AXIN2):c.366G>C (p.Leu122=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3254306	NM_004655.4(AXIN2):c.816-14T>C	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3254298	NM_004655.4(AXIN2):c.507C>A (p.Ile169=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3254295	NM_004655.4(AXIN2):c.645C>G (p.Leu215=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3254294	NM_004655.4(AXIN2):c.771C>T (p.Ala257=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3254291	NM_004655.4(AXIN2):c.318T>C (p.Asp106=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3254289	NM_004655.4(AXIN2):c.159C>G (p.Ser53=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3254287	NM_004655.4(AXIN2):c.792G>A (p.Thr264=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3254274	NM_004655.4(AXIN2):c.957-15T>C	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome	GLikely benign
Select item 3254270	NM_004655.4(AXIN2):c.735A>G (p.Pro245=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3254260	NM_004655.4(AXIN2):c.750G>A (p.Leu250=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3254257	NM_004655.4(AXIN2):c.498T>C (p.Ile166=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3254256	NM_004655.4(AXIN2):c.885C>G (p.Thr295=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3254247	NM_004655.4(AXIN2):c.420G>A (p.Glu140=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3254245	NM_004655.4(AXIN2):c.606T>C (p.Ser202=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3254244	NM_004655.4(AXIN2):c.202C>A (p.Arg68=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3254239	NM_004655.4(AXIN2):c.801T>C (p.Val267=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3254238	NM_004655.4(AXIN2):c.474A>G (p.Arg158=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3254236	NM_004655.4(AXIN2):c.144_148delinsTATGT (p.Pro50Ser)	AXIN2 (P50S)	Indel (missense variant)	Oligodontia-cancer predisposition syndrome	GBenign
Select item 3243036	NC_000017.10:g.(?_63530010)_(63554738_?)dup	AXIN2	Duplication	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 3243035	NC_000017.10:g.(?_63545628)_(63545788_?)dup	AXIN2	Duplication	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 3243034	NC_000017.10:g.(?_63553914)_(63554738_?)dup	AXIN2	Duplication	Oligodontia-cancer predisposition syndrome	GUncertain significance
Select item 3240842	NM_004655.4(AXIN2):c.1405C>G (p.His469Asp)	AXIN2 (H469D)	Single nucleotide variant (missense variant)	Colorectal cancer	GUncertain significance
Select item 3240841	NM_004655.4(AXIN2):c.128G>C (p.Gly43Ala)	AXIN2 (G43A)	Single nucleotide variant (missense variant)	Colorectal cancer	GUncertain significance
Select item 3240840	NM_004655.4(AXIN2):c.856G>C (p.Gly286Arg)	AXIN2 (G286R)	Single nucleotide variant (missense variant)	Colorectal cancer	GUncertain significance
Select item 3240839	NM_004655.4(AXIN2):c.1540_1554dup (p.Tyr518_Ile519insValHisHisHisTyr)	AXIN2	Duplication (inframe_insertion)	Colorectal cancer	GUncertain significance
Select item 3240837	NM_004655.4(AXIN2):c.184_186dup (p.Leu62_Gly63insLeu)	AXIN2	Duplication (inframe_insertion)	Colorectal cancer	GUncertain significance
Select item 3240836	NM_004655.4(AXIN2):c.1714G>C (p.Gly572Arg)	AXIN2 (G572R)	Single nucleotide variant (missense variant +1 more)	Colorectal cancer	GUncertain significance
Select item 3240835	NM_004655.4(AXIN2):c.1093G>T (p.Val365Leu)	AXIN2 (V365L)	Single nucleotide variant (missense variant)	Colorectal cancer	GUncertain significance

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