HOXA3[gene] and "single gene"[properties] - ClinVar

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Items: 37

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2460236	NM_153631.3(HOXA3):c.1310C>T (p.Ala437Val)	HOXA3 (A437V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268116	NM_153631.3(HOXA3):c.1294G>C (p.Gly432Arg)	HOXA3 (G432R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527886	NM_153631.3(HOXA3):c.1262A>G (p.Tyr421Cys)	HOXA3 (Y421C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493211	NM_153631.3(HOXA3):c.1258A>G (p.Thr420Ala)	HOXA3 (T420A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313237	NM_153631.3(HOXA3):c.1248G>C (p.Glu416Asp)	HOXA3 (E416D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106571	NM_153631.3(HOXA3):c.1243G>A (p.Gly415Arg)	HOXA3 (G415R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217131	NM_153631.3(HOXA3):c.1166C>G (p.Pro389Arg)	HOXA3 (P389R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106570	NM_153631.3(HOXA3):c.1120C>A (p.Pro374Thr)	HOXA3 (P374T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2236827	NM_153631.3(HOXA3):c.1112A>T (p.Tyr371Phe)	HOXA3 (Y371F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223559	NM_153631.3(HOXA3):c.1093G>T (p.Val365Phe)	HOXA3 (V365F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106569	NM_153631.3(HOXA3):c.1039C>T (p.His347Tyr)	HOXA3 (H347Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106568	NM_153631.3(HOXA3):c.1012G>T (p.Gly338Cys)	HOXA3 (G338C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3284633	NM_153631.3(HOXA3):c.973C>A (p.Pro325Thr)	HOXA3 (P325T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334676	NM_153631.3(HOXA3):c.954C>G (p.Ser318Arg)	HOXA3 (S318R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106579	NM_153631.3(HOXA3):c.937C>A (p.Pro313Thr)	HOXA3 (P313T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383820	NM_153631.3(HOXA3):c.910A>G (p.Thr304Ala)	HOXA3 (T304A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2546752	NM_153631.3(HOXA3):c.824G>A (p.Gly275Asp)	HOXA3 (G275D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2603224	NM_153631.3(HOXA3):c.809C>A (p.Pro270His)	HOXA3 (P270H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106578	NM_153631.3(HOXA3):c.782G>A (p.Gly261Asp)	HOXA3 (G261D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517654	NM_153631.3(HOXA3):c.676A>G (p.Asn226Asp)	HOXA3 (N226D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106577	NM_153631.3(HOXA3):c.637A>C (p.Asn213His)	HOXA3 (N213H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106576	NM_153631.3(HOXA3):c.632A>T (p.His211Leu)	HOXA3 (H211L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341343	NM_153631.3(HOXA3):c.569C>G (p.Ser190Trp)	HOXA3 (S190W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261085	NM_153631.3(HOXA3):c.445C>T (p.Pro149Ser)	HOXA3 (P149S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537726	NM_153631.3(HOXA3):c.430C>T (p.Pro144Ser)	HOXA3 (P144S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530129	NM_153631.3(HOXA3):c.419C>T (p.Ala140Val)	HOXA3 (A140V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106575	NM_153631.3(HOXA3):c.332C>T (p.Pro111Leu)	HOXA3 (P111L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2657361	NM_153631.3(HOXA3):c.321C>A (p.Pro107=)	HOXA3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3106574	NM_153631.3(HOXA3):c.305C>T (p.Pro102Leu)	HOXA3 (P102L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332859	NM_153631.3(HOXA3):c.304C>T (p.Pro102Ser)	HOXA3 (P102S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279347	NM_153631.3(HOXA3):c.263C>A (p.Pro88Gln)	HOXA3 (P88Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487806	NM_153631.3(HOXA3):c.256G>A (p.Gly86Arg)	HOXA3 (G86R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106572	NM_153631.3(HOXA3):c.242A>G (p.Gln81Arg)	HOXA3 (Q81R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306027	NM_153631.3(HOXA3):c.176G>A (p.Gly59Glu)	HOXA3 (G59E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2472348	NM_153631.3(HOXA3):c.127G>A (p.Gly43Ser)	HOXA3 (G43S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2269745	NM_153631.3(HOXA3):c.110C>T (p.Ala37Val)	HOXA3 (A37V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 1301789	NM_153631.3(HOXA3):c.-121+3042C>G	HOXA3	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GBenign

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Items: 37