"Genome Diagnostics Laboratory, Amsterdam University Medical Center"[s - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 220937	NM_004655.4(AXIN2):c.2124G>C (p.Ser708=)	AXIN2	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
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 136484	NM_004655.4(AXIN2):c.1615G>A (p.Val539Met)	AXIN2 (V539M)	Single nucleotide variant (missense variant)	not specified +4 more	GBenign/Likely benign
Select item 136481	NM_004655.4(AXIN2):c.1530G>A (p.Thr510=)	AXIN2	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign
Select item 464546	NM_004655.4(AXIN2):c.1404CCA[5] (p.His474del)	AXIN2 (H474del)	Microsatellite (inframe_deletion)	Oligodontia-cancer predisposition syndrome +3 more	GConflicting classifications of pathogenicity
Select item 136480	NM_004655.4(AXIN2):c.1410C>T (p.His470=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome +3 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 136479	NM_004655.4(AXIN2):c.1305G>A (p.Pro435=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing 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)	not provided +4 more	GBenign/Likely benign
Select item 136476	NM_004655.4(AXIN2):c.1101C>T (p.Pro367=)	AXIN2	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign
Select item 239976	NM_004655.4(AXIN2):c.1092C>T (p.Pro364=)	AXIN2	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 127948	NM_004655.4(AXIN2):c.733C>T (p.Pro245Ser)	AXIN2 (P245S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 240028	NM_004655.4(AXIN2):c.721T>G (p.Cys241Gly)	AXIN2 (C241G)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +3 more	GConflicting classifications of pathogenicity
Select item 377542	NM_004655.4(AXIN2):c.645C>T (p.Leu215=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome +2 more	GBenign/Likely benign