"Ambry Genetics"[submitter] AND "STARD9"[gene] - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 1 to 100 of 238

<< First< Prev

Page of 3

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2542466	NM_020759.3(STARD9):c.70A>G (p.Ile24Val)	STARD9 (I24V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2350746	NM_020759.3(STARD9):c.158A>G (p.Lys53Arg)	STARD9 (K53R)	Single nucleotide variant (missense variant)	STARD9-related condition +1 more	GConflicting classifications of pathogenicity
Select item 2559873	NM_020759.3(STARD9):c.431G>A (p.Cys144Tyr)	STARD9 (C144Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2282526	NM_020759.3(STARD9):c.460T>C (p.Tyr154His)	STARD9 (Y154H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2305349	NM_020759.3(STARD9):c.470G>A (p.Arg157Gln)	STARD9 (R157Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2349895	NM_020759.3(STARD9):c.509C>G (p.Ser170Cys)	STARD9 (S170C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2491357	NM_020759.3(STARD9):c.521G>A (p.Arg174Gln)	STARD9 (R174Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2619513	NM_020759.3(STARD9):c.548C>T (p.Pro183Leu)	STARD9 (P183L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2536261	NM_020759.3(STARD9):c.680T>G (p.Ile227Ser)	STARD9 (I227S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2530988	NM_020759.3(STARD9):c.686C>A (p.Thr229Lys)	STARD9 (T229K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2490510	NM_020759.3(STARD9):c.721C>T (p.Leu241Phe)	STARD9 (L241F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2314527	NM_020759.3(STARD9):c.880C>G (p.Gln294Glu)	STARD9 (Q294E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2367373	NM_020759.3(STARD9):c.1042A>G (p.Ser348Gly)	STARD9 (S348G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2261350	NM_020759.3(STARD9):c.1105A>C (p.Ser369Arg)	STARD9 (S369R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2617315	NM_020759.3(STARD9):c.1135T>C (p.Ser379Pro)	STARD9 (S379P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2329223	NM_020759.3(STARD9):c.1293G>C (p.Glu431Asp)	STARD9 (E431D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2329224	NM_020759.3(STARD9):c.1294C>A (p.Leu432Met)	STARD9 (L432M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2274159	NM_020759.3(STARD9):c.1396A>C (p.Asn466His)	STARD9 (N466H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2335771	NM_020759.3(STARD9):c.1529C>T (p.Ser510Leu)	STARD9 (S510L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2597000	NM_020759.3(STARD9):c.1610T>C (p.Val537Ala)	STARD9 (V537A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2390194	NM_020759.3(STARD9):c.1628G>A (p.Arg543His)	STARD9 (R543H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2213554	NM_020759.3(STARD9):c.1636C>T (p.Arg546Cys)	STARD9 (R546C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 807220	NM_020759.3(STARD9):c.1655G>T (p.Arg552Leu)	STARD9 (R552L)	Single nucleotide variant (missense variant)	STARD9-related condition +2 more	GConflicting classifications of pathogenicity
Select item 2207397	NM_020759.3(STARD9):c.1666G>T (p.Ala556Ser)	STARD9 (A556S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2257228	NM_020759.3(STARD9):c.1676G>A (p.Arg559His)	STARD9 (R559H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2473131	NM_020759.3(STARD9):c.1763G>A (p.Arg588Gln)	STARD9 (R588Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2608706	NM_020759.3(STARD9):c.1768C>A (p.Gln590Lys)	STARD9 (Q590K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2291408	NM_020759.3(STARD9):c.1820A>G (p.Asp607Gly)	STARD9 (D607G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2597202	NM_020759.3(STARD9):c.1916C>T (p.Pro639Leu)	STARD9 (P639L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2462194	NM_020759.3(STARD9):c.2125G>A (p.Glu709Lys)	STARD9 (E709K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2244350	NM_020759.3(STARD9):c.2254C>T (p.Arg752Trp)	STARD9 (R752W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2471554	NM_020759.3(STARD9):c.2293C>T (p.Arg765Trp)	STARD9 (R765W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2240896	NM_020759.3(STARD9):c.2410G>A (p.Glu804Lys)	STARD9 (E804K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2273209	NM_020759.3(STARD9):c.2495G>A (p.Ser832Asn)	STARD9 (S832N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2378211	NM_020759.3(STARD9):c.2587C>T (p.Pro863Ser)	STARD9 (P863S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2277641	NM_020759.3(STARD9):c.2648A>G (p.Tyr883Cys)	STARD9 (Y883C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2556197	NM_020759.3(STARD9):c.2659A>G (p.Thr887Ala)	STARD9 (T887A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2373520	NM_020759.3(STARD9):c.3010G>A (p.Gly1004Arg)	STARD9 (G1004R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2533114	NM_020759.3(STARD9):c.3089C>G (p.Thr1030Arg)	STARD9 (T1030R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2296439	NM_020759.3(STARD9):c.3188C>T (p.Pro1063Leu)	STARD9 (P1063L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2596530	NM_020759.3(STARD9):c.3208A>G (p.Arg1070Gly)	STARD9 (R1070G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2274705	NM_020759.3(STARD9):c.3240G>A (p.Met1080Ile)	STARD9 (M1080I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2319372	NM_020759.3(STARD9):c.3247C>T (p.Leu1083Phe)	STARD9 (L1083F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2204973	NM_020759.3(STARD9):c.3422G>A (p.Ser1141Asn)	STARD9 (S1141N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2241891	NM_020759.3(STARD9):c.3436C>G (p.Leu1146Val)	STARD9 (L1146V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2463065	NM_020759.3(STARD9):c.3494G>A (p.Gly1165Asp)	STARD9 (G1165D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2354877	NM_020759.3(STARD9):c.3526A>T (p.Arg1176Trp)	STARD9 (R1176W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2474289	NM_020759.3(STARD9):c.3589C>G (p.Gln1197Glu)	STARD9 (Q1197E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2250650	NM_020759.3(STARD9):c.3691C>A (p.Pro1231Thr)	STARD9 (P1231T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2549759	NM_020759.3(STARD9):c.3937A>T (p.Ser1313Cys)	STARD9 (S1313C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2231556	NM_020759.3(STARD9):c.4003A>G (p.Met1335Val)	STARD9 (M1335V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2239752	NM_020759.3(STARD9):c.4063G>C (p.Gly1355Arg)	STARD9 (G1355R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2410839	NM_020759.3(STARD9):c.4064G>A (p.Gly1355Asp)	STARD9 (G1355D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2595353	NM_020759.3(STARD9):c.4076C>G (p.Pro1359Arg)	STARD9 (P1359R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2619386	NM_020759.3(STARD9):c.4196A>C (p.His1399Pro)	STARD9 (H1399P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2203807	NM_020759.3(STARD9):c.4297C>A (p.Gln1433Lys)	STARD9 (Q1433K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2556261	NM_020759.3(STARD9):c.4301C>T (p.Pro1434Leu)	STARD9 (P1434L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2594393	NM_020759.3(STARD9):c.4397T>C (p.Leu1466Pro)	STARD9 (L1466P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2473345	NM_020759.3(STARD9):c.4622A>G (p.Asn1541Ser)	STARD9 (N1541S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2475430	NM_020759.3(STARD9):c.4623T>G (p.Asn1541Lys)	STARD9 (N1541K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2459180	NM_020759.3(STARD9):c.4624C>G (p.Leu1542Val)	STARD9 (L1542V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2328134	NM_020759.3(STARD9):c.4670T>C (p.Leu1557Ser)	STARD9 (L1557S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2395640	NM_020759.3(STARD9):c.4693A>G (p.Ser1565Gly)	STARD9 (S1565G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2221630	NM_020759.3(STARD9):c.4790T>C (p.Leu1597Ser)	STARD9 (L1597S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2406612	NM_020759.3(STARD9):c.4840A>G (p.Ile1614Val)	STARD9 (I1614V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2372273	NM_020759.3(STARD9):c.4856C>T (p.Thr1619Ile)	STARD9 (T1619I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2553188	NM_020759.3(STARD9):c.4906T>A (p.Cys1636Ser)	STARD9 (C1636S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2607481	NM_020759.3(STARD9):c.4960G>A (p.Ala1654Thr)	STARD9 (A1654T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2266701	NM_020759.3(STARD9):c.4975G>T (p.Val1659Phe)	STARD9 (V1659F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2517569	NM_020759.3(STARD9):c.5075A>G (p.Tyr1692Cys)	STARD9 (Y1692C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2344335	NM_020759.3(STARD9):c.5116A>G (p.Lys1706Glu)	STARD9 (K1706E)	Single nucleotide variant (missense variant)	STARD9-related condition +1 more	GConflicting classifications of pathogenicity
Select item 2255048	NM_020759.3(STARD9):c.5144T>C (p.Val1715Ala)	STARD9 (V1715A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2494221	NM_020759.3(STARD9):c.5159C>T (p.Pro1720Leu)	STARD9 (P1720L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2332918	NM_020759.3(STARD9):c.5263G>A (p.Ala1755Thr)	STARD9 (A1755T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2238623	NM_020759.3(STARD9):c.5290C>G (p.Pro1764Ala)	STARD9 (P1764A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2271255	NM_020759.3(STARD9):c.5327C>A (p.Pro1776His)	STARD9 (P1776H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2604979	NM_020759.3(STARD9):c.5354A>G (p.Asn1785Ser)	STARD9 (N1785S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2358586	NM_020759.3(STARD9):c.5375C>T (p.Ala1792Val)	STARD9 (A1792V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2360244	NM_020759.3(STARD9):c.5450C>G (p.Ala1817Gly)	STARD9 (A1817G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2264278	NM_020759.3(STARD9):c.5492A>T (p.Glu1831Val)	STARD9 (E1831V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2603744	NM_020759.3(STARD9):c.5555C>T (p.Thr1852Ile)	STARD9 (T1852I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2353133	NM_020759.3(STARD9):c.5743G>T (p.Ala1915Ser)	STARD9 (A1915S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2236441	NM_020759.3(STARD9):c.5831C>G (p.Ala1944Gly)	STARD9 (A1944G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2555102	NM_020759.3(STARD9):c.5848A>G (p.Arg1950Gly)	STARD9 (R1950G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2551717	NM_020759.3(STARD9):c.5857G>C (p.Asp1953His)	STARD9 (D1953H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2248961	NM_020759.3(STARD9):c.5858A>G (p.Asp1953Gly)	STARD9 (D1953G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2310861	NM_020759.3(STARD9):c.5879T>C (p.Val1960Ala)	STARD9 (V1960A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2231579	NM_020759.3(STARD9):c.5927A>G (p.Asn1976Ser)	STARD9 (N1976S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2268978	NM_020759.3(STARD9):c.5930A>C (p.Glu1977Ala)	STARD9 (E1977A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2406730	NM_020759.3(STARD9):c.5945A>C (p.Glu1982Ala)	STARD9 (E1982A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2379573	NM_020759.3(STARD9):c.5945A>G (p.Glu1982Gly)	STARD9 (E1982G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2547332	NM_020759.3(STARD9):c.5965G>C (p.Asp1989His)	STARD9 (D1989H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2216999	NM_020759.3(STARD9):c.6020A>T (p.Gln2007Leu)	STARD9 (Q2007L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2376450	NM_020759.3(STARD9):c.6065C>T (p.Ser2022Leu)	STARD9 (S2022L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2223660	NM_020759.3(STARD9):c.6124A>G (p.Asn2042Asp)	STARD9 (N2042D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2510164	NM_020759.3(STARD9):c.6242A>G (p.Asp2081Gly)	STARD9 (D2081G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2508286	NM_020759.3(STARD9):c.6274C>G (p.Gln2092Glu)	STARD9 (Q2092E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2355691	NM_020759.3(STARD9):c.6301C>T (p.Pro2101Ser)	STARD9 (P2101S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2334340	NM_020759.3(STARD9):c.6310T>G (p.Ser2104Ala)	STARD9 (S2104A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2537667	NM_020759.3(STARD9):c.6424C>T (p.Pro2142Ser)	STARD9 (P2142S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

<< First< Prev

Page of 3