"KCCC/NGS Laboratory, Kuwait Cancer Control Center"[submitter] AND "AX - ClinVar

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Items: 32

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 240010	NM_004655.4(AXIN2):c.2213C>T (p.Ser738Phe)	AXIN2 (S738F +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
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 182018	NM_004655.4(AXIN2):c.2013_2024del (p.Thr672_Arg675del)	AXIN2	Deletion (inframe_deletion)	not provided +3 more	GBenign
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 259513	NM_004655.4(AXIN2):c.1907+39T>A	AXIN2	Single nucleotide variant (intron variant)	Oligodontia-cancer predisposition syndrome +2 more	GBenign
Select item 1026453	NM_004655.4(AXIN2):c.1855G>A (p.Val619Ile)	AXIN2 (V619I)	Single nucleotide variant (missense variant +1 more)	Oligodontia-cancer predisposition syndrome	GUncertain significance
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 415223	NM_004655.4(AXIN2):c.1803C>T (p.Gly601=)	AXIN2	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GBenign/Likely 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 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 239992	NM_004655.4(AXIN2):c.1599G>A (p.Ala533=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 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 136481	NM_004655.4(AXIN2):c.1530G>A (p.Thr510=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome +3 more	GBenign/Likely benign
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 415213	NM_004655.4(AXIN2):c.1380T>C (p.Tyr460=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +3 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 464540	NM_004655.4(AXIN2):c.1356C>T (p.Cys452=)	AXIN2	Single nucleotide variant (synonymous variant)	Oligodontia-cancer predisposition syndrome +1 more	GBenign/Likely benign
Select item 136478	NM_004655.4(AXIN2):c.1250C>T (p.Ala417Val)	AXIN2 (A417V)	Single nucleotide variant (missense variant)	Oligodontia-cancer predisposition syndrome +3 more	GBenign/Likely benign
Select item 324649	NM_004655.4(AXIN2):c.1242G>A (p.Arg414=)	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)	Oligodontia-cancer predisposition syndrome +4 more	GBenign/Likely benign
Select item 136476	NM_004655.4(AXIN2):c.1101C>T (p.Pro367=)	AXIN2	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 136475	NM_004655.4(AXIN2):c.1059+8C>T	AXIN2	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
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 383383	NM_004655.4(AXIN2):c.435C>G (p.Val145=)	AXIN2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GBenign/Likely benign
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 949202	NM_004655.4(AXIN2):c.395A>G (p.Lys132Arg)	AXIN2 (K132R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
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