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

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Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3263131	NM_001746.4(CANX):c.58G>T (p.Ala20Ser)	CANX (A55S +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2406083	NM_001746.4(CANX):c.87T>G (p.Ile29Met)	CANX (I64M +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2308584	NM_001746.4(CANX):c.100G>C (p.Asp34His)	CANX (D69H +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3136984	NM_001746.4(CANX):c.146C>T (p.Thr49Ile)	CANX (T103I +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2362067	NM_001746.4(CANX):c.241T>G (p.Ser81Ala)	CANX (S116A +2 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3263128	NM_001746.4(CANX):c.280G>A (p.Asp94Asn)	CANX (D148N +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3136986	NM_001746.4(CANX):c.419T>A (p.Leu140Gln)	CANX (L140Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3136987	NM_001746.4(CANX):c.425A>G (p.Asp142Gly)	CANX (D177G +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2529785	NM_001746.4(CANX):c.617A>G (p.His206Arg)	CANX (H260R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2238837	NM_001746.4(CANX):c.620A>G (p.Lys207Arg)	CANX (K207R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2604306	NM_001746.4(CANX):c.766G>A (p.Val256Met)	CANX (V310M +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3136988	NM_001746.4(CANX):c.805C>T (p.Pro269Ser)	CANX (P161S +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2252617	NM_001746.4(CANX):c.830A>G (p.Glu277Gly)	CANX (E311G +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2215229	NM_001746.4(CANX):c.961G>A (p.Glu321Lys)	CANX (E355K +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3136989	NM_001746.4(CANX):c.991G>A (p.Val331Ile)	CANX (V385I +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2543819	NM_001746.4(CANX):c.1004A>G (p.Asp335Gly)	CANX (D227G +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3136980	NM_001746.4(CANX):c.1006G>A (p.Ala336Thr)	CANX (A336T +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3136981	NM_001746.4(CANX):c.1063A>G (p.Ile355Val)	CANX (I247V +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2367941	NM_001746.4(CANX):c.1102G>A (p.Val368Ile)	CANX (V368I +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3136982	NM_001746.4(CANX):c.1195C>G (p.Pro399Ala)	CANX (P399A +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3263130	NM_001746.4(CANX):c.1214C>A (p.Pro405Gln)	CANX (P439Q +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2318803	NM_001746.4(CANX):c.1262C>T (p.Ala421Val)	CANX (A455V +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2537696	NM_001746.4(CANX):c.1355A>G (p.Asn452Ser)	CANX (N506S +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3136983	NM_001746.4(CANX):c.1405G>A (p.Val469Ile)	CANX (V503I +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3263127	NM_001746.4(CANX):c.1442C>T (p.Pro481Leu)	CANX (P515L +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3263129	NM_001746.4(CANX):c.1490T>C (p.Leu497Pro)	CANX (L531P +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2279242	NM_001746.4(CANX):c.1532G>A (p.Gly511Asp)	CANX (G403D +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3136985	NM_001746.4(CANX):c.1670A>C (p.Glu557Ala)	CANX (E592A +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2388347	NM_001746.4(CANX):c.1678G>A (p.Gly560Ser)	CANX (G594S +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 29