LARP1B[gene] and "single gene"[properties] - ClinVar

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Items: 56

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2509315	NM_018078.4(LARP1B):c.183G>C (p.Glu61Asp)	LARP1B (E61D)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3117829	NM_018078.4(LARP1B):c.213G>C (p.Lys71Asn)	LARP1B (K71N)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3117833	NM_018078.4(LARP1B):c.434G>A (p.Arg145Gln)	LARP1B (R145Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2228535	NM_018078.4(LARP1B):c.464G>A (p.Arg155Gln)	LARP1B (R155Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2214810	NM_018078.4(LARP1B):c.469C>T (p.Arg157Trp)	LARP1B (R157W)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2313701	NM_018078.4(LARP1B):c.524G>A (p.Gly175Asp)	LARP1B (G175D)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2514850	NM_018078.4(LARP1B):c.587T>C (p.Met196Thr)	LARP1B (M196T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2408089	NM_018078.4(LARP1B):c.596A>G (p.Tyr199Cys)	LARP1B (Y199C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2213805	NM_018078.4(LARP1B):c.619G>A (p.Val207Met)	LARP1B (V207M)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3117834	NM_018078.4(LARP1B):c.628G>C (p.Val210Leu)	LARP1B (V210L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3117835	NM_018078.4(LARP1B):c.671A>G (p.Glu224Gly)	LARP1B (E224G)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2337681	NM_018078.4(LARP1B):c.672A>C (p.Glu224Asp)	LARP1B (E224D)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3117836	NM_018078.4(LARP1B):c.731A>C (p.Glu244Ala)	LARP1B (E3A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3117837	NM_018078.4(LARP1B):c.896G>A (p.Gly299Asp)	LARP1B (G58D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3117838	NM_018078.4(LARP1B):c.907C>T (p.Arg303Cys)	LARP1B (R303C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2296380	NM_018078.4(LARP1B):c.925G>C (p.Asp309His)	LARP1B (D309H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2405328	NM_018078.4(LARP1B):c.941T>C (p.Ile314Thr)	LARP1B (I314T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2210743	NM_018078.4(LARP1B):c.971C>A (p.Ala324Asp)	LARP1B (A83D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2622409	NM_018078.4(LARP1B):c.983A>T (p.His328Leu)	LARP1B (H328L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2382859	NM_018078.4(LARP1B):c.997C>G (p.Pro333Ala)	LARP1B (P333A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2294120	NM_018078.4(LARP1B):c.1021C>T (p.Pro341Ser)	LARP1B (P341S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2381770	NM_018078.4(LARP1B):c.1066A>G (p.Met356Val)	LARP1B (M115V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3117821	NM_018078.4(LARP1B):c.1106C>T (p.Ser369Leu)	LARP1B (S128L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2519923	NM_018078.4(LARP1B):c.1117A>G (p.Ile373Val)	LARP1B (I132V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3117822	NM_018078.4(LARP1B):c.1203T>G (p.Cys401Trp)	LARP1B (C160W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2307422	NM_018078.4(LARP1B):c.1217C>T (p.Pro406Leu)	LARP1B (P406L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3117823	NM_018078.4(LARP1B):c.1255A>T (p.Ile419Phe)	LARP1B (I178F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 161836	NM_018078.4(LARP1B):c.1324G>T (p.Asp442Tyr)	LARP1B (D442Y +1 more)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 3117824	NM_018078.4(LARP1B):c.1372G>A (p.Val458Met)	LARP1B (V217M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2220398	NM_018078.4(LARP1B):c.1411A>G (p.Met471Val)	LARP1B (M230V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2265221	NM_018078.4(LARP1B):c.1456G>C (p.Asp486His)	LARP1B (D245H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2472822	NM_018078.4(LARP1B):c.1493A>C (p.Glu498Ala)	LARP1B (E257A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2262561	NM_018078.4(LARP1B):c.1495G>A (p.Glu499Lys)	LARP1B (E258K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2380982	NM_018078.4(LARP1B):c.1497A>T (p.Glu499Asp)	LARP1B (E499D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2221887	NM_018078.4(LARP1B):c.1560T>G (p.Ile520Met)	LARP1B (I279M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3117825	NM_018078.4(LARP1B):c.1733C>T (p.Thr578Ile)	LARP1B (T578I +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2512126	NM_018078.4(LARP1B):c.1826G>T (p.Arg609Met)	LARP1B (R597M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2294363	NM_018078.4(LARP1B):c.1931A>G (p.Asn644Ser)	LARP1B (N632S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2258565	NM_018078.4(LARP1B):c.1937C>T (p.Pro646Leu)	LARP1B (P366L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2265125	NM_018078.4(LARP1B):c.1991C>A (p.Thr664Lys)	LARP1B (T384K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3117827	NM_018078.4(LARP1B):c.2032G>A (p.Ala678Thr)	LARP1B (A666T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3117828	NM_018078.4(LARP1B):c.2130A>C (p.Gln710His)	LARP1B (Q430H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2258532	NM_018078.4(LARP1B):c.2147G>A (p.Arg716His)	LARP1B (R436H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2608743	NM_018078.4(LARP1B):c.2173C>T (p.Arg725Cys)	LARP1B (R445C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3117830	NM_018078.4(LARP1B):c.2216G>A (p.Arg739His)	LARP1B (R727H +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2392005	NM_018078.4(LARP1B):c.2259G>A (p.Met753Ile)	LARP1B (M20I +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2470843	NM_018078.4(LARP1B):c.2369G>A (p.Arg790Gln)	LARP1B (R510Q +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3117831	NM_018078.4(LARP1B):c.2413G>A (p.Glu805Lys)	LARP1B (E525K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553093	NM_018078.4(LARP1B):c.2423A>T (p.Gln808Leu)	LARP1B (Q75L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2530778	NM_018078.4(LARP1B):c.2429A>G (p.Tyr810Cys)	LARP1B (Y798C +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2299549	NM_018078.4(LARP1B):c.2590A>G (p.Thr864Ala)	LARP1B (T852A +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2490575	NM_018078.4(LARP1B):c.2609A>G (p.Asn870Ser)	LARP1B (N590S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3117832	NM_018078.4(LARP1B):c.2705G>T (p.Arg902Ile)	LARP1B (R622I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2472688	NM_018078.4(LARP1B):c.2711A>G (p.Asn904Ser)	LARP1B (N892S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2329414	NM_018078.4(LARP1B):c.2720C>A (p.Pro907Gln)	LARP1B (P174Q +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2375922	NM_018078.4(LARP1B):c.2741A>G (p.His914Arg)	LARP1B (H914R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 56