ANAPC2[gene] and "single gene"[properties] - ClinVar

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Items: 38

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3117812	NM_013366.4(ANAPC2):c.2275C>A (p.Gln759Lys)	ANAPC2 (Q759K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3293840	NM_013366.4(ANAPC2):c.2267C>T (p.Thr756Met)	ANAPC2 (T756M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2240643	NM_013366.4(ANAPC2):c.2246A>G (p.Glu749Gly)	ANAPC2 (E749G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3117807	NM_013366.4(ANAPC2):c.2188A>G (p.Ile730Val)	ANAPC2 (I730V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3117805	NM_013366.4(ANAPC2):c.2186T>C (p.Leu729Pro)	ANAPC2 (L729P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310430	NM_013366.4(ANAPC2):c.2134A>G (p.Thr712Ala)	ANAPC2 (T712A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3117800	NM_013366.4(ANAPC2):c.2131G>A (p.Gly711Ser)	ANAPC2 (G711S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3117797	NM_013366.4(ANAPC2):c.2124G>T (p.Glu708Asp)	ANAPC2 (E708D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2659813	NM_013366.4(ANAPC2):c.2091C>T (p.Ser697=)	ANAPC2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3117791	NM_013366.4(ANAPC2):c.2035G>A (p.Glu679Lys)	ANAPC2 (E679K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303634	NM_013366.4(ANAPC2):c.2018A>G (p.Gln673Arg)	ANAPC2 (Q673R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 787588	NM_013366.4(ANAPC2):c.1992G>A (p.Ala664=)	ANAPC2	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 3293830	NM_013366.4(ANAPC2):c.1753G>C (p.Glu585Gln)	ANAPC2 (E585Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489184	NM_013366.4(ANAPC2):c.1744C>T (p.Pro582Ser)	ANAPC2 (P582S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247423	NM_013366.4(ANAPC2):c.1730A>G (p.Glu577Gly)	ANAPC2 (E577G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362562	NM_013366.4(ANAPC2):c.1724G>A (p.Arg575Gln)	ANAPC2 (R575Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 776484	NM_013366.4(ANAPC2):c.1527C>T (p.Tyr509=)	ANAPC2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2399181	NM_013366.4(ANAPC2):c.1465C>G (p.Pro489Ala)	ANAPC2 (P489A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2619861	NM_013366.4(ANAPC2):c.1388G>C (p.Ser463Thr)	ANAPC2 (S463T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356315	NM_013366.4(ANAPC2):c.1277G>A (p.Arg426His)	ANAPC2 (R426H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3117767	NM_013366.4(ANAPC2):c.1193C>G (p.Thr398Ser)	ANAPC2 (T398S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491095	NM_013366.4(ANAPC2):c.1169G>C (p.Gly390Ala)	ANAPC2 (G390A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3117762	NM_013366.4(ANAPC2):c.1144C>G (p.Leu382Val)	ANAPC2 (L382V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305683	NM_013366.4(ANAPC2):c.968G>A (p.Arg323His)	ANAPC2 (R323H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223802	NM_013366.4(ANAPC2):c.967C>T (p.Arg323Cys)	ANAPC2 (R323C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262538	NM_013366.4(ANAPC2):c.944C>T (p.Pro315Leu)	ANAPC2 (P315L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305086	NM_013366.4(ANAPC2):c.902G>C (p.Gly301Ala)	ANAPC2 (G301A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593831	NM_013366.4(ANAPC2):c.901G>A (p.Gly301Ser)	ANAPC2 (G301S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3117839	NM_013366.4(ANAPC2):c.859C>T (p.Arg287Cys)	ANAPC2 (R287C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297145	NM_013366.4(ANAPC2):c.816G>T (p.Arg272Ser)	ANAPC2 (R272S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275524	NM_013366.4(ANAPC2):c.808C>T (p.Arg270Trp)	ANAPC2 (R270W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616102	NM_013366.4(ANAPC2):c.629G>A (p.Arg210His)	ANAPC2 (R210H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528029	NM_013366.4(ANAPC2):c.454G>A (p.Glu152Lys)	ANAPC2 (E152K)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3117816	NM_013366.4(ANAPC2):c.443G>A (p.Gly148Glu)	ANAPC2 (G148E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3293823	NM_013366.4(ANAPC2):c.362G>T (p.Arg121Leu)	ANAPC2 (R121L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284565	NM_013366.4(ANAPC2):c.257A>G (p.Asn86Ser)	ANAPC2 (N86S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3117778	NM_013366.4(ANAPC2):c.167G>A (p.Arg56Gln)	ANAPC2 (R56Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3117826	NM_013366.4(ANAPC2):c.79G>A (p.Val27Met)	ANAPC2 (V27M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 38