"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "AXIN2"[gene] - ClinVar

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Items: 32

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 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 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 259514	NM_004655.4(AXIN2):c.2062C>T (p.Leu688=)	AXIN2	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign
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 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 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 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 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 533169	NM_004655.4(AXIN2):c.1927G>C (p.Ala643Pro)	AXIN2 (A643P +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 492673	NM_004655.4(AXIN2):c.1908-21C>G	AXIN2	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 136485	NM_004655.4(AXIN2):c.1713-18G>A	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome +2 more	GBenign/Likely benign
Select item 259512	NM_004655.4(AXIN2):c.1712+19G>T	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome +2 more	GBenign
Select item 842068	NM_004655.4(AXIN2):c.1665C>G (p.Cys555Trp)	AXIN2 (C555W)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 533180	NM_004655.4(AXIN2):c.1628G>T (p.Cys543Phe)	AXIN2 (C543F)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +2 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 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 408823	NM_004655.4(AXIN2):c.1553A>G (p.Tyr518Cys)	AXIN2 (Y518C)	Single nucleotide variant (missense variant)	not specified +4 more	GConflicting classifications of pathogenicity
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 136480	NM_004655.4(AXIN2):c.1410C>T (p.His470=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign
Select item 259510	NM_004655.4(AXIN2):c.1386C>T (p.Pro462=)	AXIN2	Single nucleotide variant (synonymous variant)	not provided +4 more	GBenign
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 259509	NM_004655.4(AXIN2):c.1365A>G (p.Pro455=)	AXIN2	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign
Select item 127935	NM_004655.4(AXIN2):c.1235A>C (p.Asn412Thr)	AXIN2 (N412T)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
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 259516	NM_004655.4(AXIN2):c.956+16A>G	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome +2 more	GBenign
Select item 418888	NM_004655.4(AXIN2):c.895G>A (p.Asp299Asn)	AXIN2 (D299N)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 259515	NM_004655.4(AXIN2):c.432T>C (p.Ile144=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome +3 more	GBenign
Select item 136490	NM_004655.4(AXIN2):c.270C>T (p.Asp90=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
Select item 259511	NM_004655.4(AXIN2):c.148C>T (p.Pro50Ser)	AXIN2 (P50S)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign
Select item 384894	NM_004655.4(AXIN2):c.135C>T (p.Val45=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity

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Items: 32