"Ambry Genetics"[submitter] AND "BOD1L1"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2292947	NM_148894.3(BOD1L1):c.9101G>A (p.Arg3034Gln)	BOD1L1 (R3034Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2533318	NM_148894.3(BOD1L1):c.9071G>A (p.Arg3024His)	BOD1L1 (R3024H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2533194	NM_148894.3(BOD1L1):c.8943G>T (p.Lys2981Asn)	BOD1L1 (K2981N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2601752	NM_148894.3(BOD1L1):c.8909G>T (p.Arg2970Leu)	BOD1L1 (R2970L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2459332	NM_148894.3(BOD1L1):c.8834G>A (p.Arg2945His)	BOD1L1 (R2945H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2251918	NM_148894.3(BOD1L1):c.8807G>A (p.Gly2936Asp)	BOD1L1 (G2936D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2328191	NM_148894.3(BOD1L1):c.8765A>C (p.Glu2922Ala)	BOD1L1 (E2922A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2330779	NM_148894.3(BOD1L1):c.8761A>G (p.Lys2921Glu)	BOD1L1 (K2921E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2267998	NM_148894.3(BOD1L1):c.8554C>G (p.Pro2852Ala)	BOD1L1 (P2852A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2383018	NM_148894.3(BOD1L1):c.8542A>G (p.Thr2848Ala)	BOD1L1 (T2848A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2324632	NM_148894.3(BOD1L1):c.8524T>C (p.Tyr2842His)	BOD1L1 (Y2842H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2215090	NM_148894.3(BOD1L1):c.8519A>G (p.Asp2840Gly)	BOD1L1 (D2840G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2510492	NM_148894.3(BOD1L1):c.8515A>G (p.Lys2839Glu)	BOD1L1 (K2839E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2376668	NM_148894.3(BOD1L1):c.8494A>T (p.Thr2832Ser)	BOD1L1 (T2832S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2489190	NM_148894.3(BOD1L1):c.8492C>T (p.Thr2831Ile)	BOD1L1 (T2831I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2284293	NM_148894.3(BOD1L1):c.8465C>A (p.Pro2822His)	BOD1L1 (P2822H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2392091	NM_148894.3(BOD1L1):c.8414C>T (p.Thr2805Met)	BOD1L1 (T2805M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2471046	NM_148894.3(BOD1L1):c.8327A>T (p.His2776Leu)	BOD1L1 (H2776L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2303183	NM_148894.3(BOD1L1):c.8294A>G (p.Glu2765Gly)	BOD1L1 (E2765G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2472948	NM_148894.3(BOD1L1):c.8183T>C (p.Ile2728Thr)	BOD1L1 (I2728T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2268103	NM_148894.3(BOD1L1):c.7996C>G (p.Leu2666Val)	BOD1L1 (L2666V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2332377	NM_148894.3(BOD1L1):c.7891T>G (p.Ser2631Ala)	BOD1L1 (S2631A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2238254	NM_148894.3(BOD1L1):c.7882A>C (p.Thr2628Pro)	BOD1L1 (T2628P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2259418	NM_148894.3(BOD1L1):c.7858G>A (p.Glu2620Lys)	BOD1L1 (E2620K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2593936	NM_148894.3(BOD1L1):c.7837T>G (p.Trp2613Gly)	BOD1L1 (W2613G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2462420	NM_148894.3(BOD1L1):c.7774G>A (p.Val2592Ile)	BOD1L1 (V2592I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2211432	NM_148894.3(BOD1L1):c.7774G>T (p.Val2592Leu)	BOD1L1 (V2592L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2385473	NM_148894.3(BOD1L1):c.7676C>T (p.Ser2559Phe)	BOD1L1 (S2559F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2514703	NM_148894.3(BOD1L1):c.7636G>A (p.Val2546Met)	BOD1L1 (V2546M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2370024	NM_148894.3(BOD1L1):c.7594G>A (p.Gly2532Ser)	BOD1L1 (G2532S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2475053	NM_148894.3(BOD1L1):c.7570C>T (p.Arg2524Cys)	BOD1L1 (R2524C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2357607	NM_148894.3(BOD1L1):c.7445G>C (p.Gly2482Ala)	BOD1L1 (G2482A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2615292	NM_148894.3(BOD1L1):c.7354A>G (p.Ser2452Gly)	BOD1L1 (S2452G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2593218	NM_148894.3(BOD1L1):c.7213G>A (p.Glu2405Lys)	BOD1L1 (E2405K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2402401	NM_148894.3(BOD1L1):c.7093G>C (p.Ala2365Pro)	BOD1L1 (A2365P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2290699	NM_148894.3(BOD1L1):c.7018A>G (p.Ile2340Val)	BOD1L1 (I2340V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2599145	NM_148894.3(BOD1L1):c.6985A>G (p.Ile2329Val)	BOD1L1 (I2329V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2355446	NM_148894.3(BOD1L1):c.6932A>G (p.Gln2311Arg)	BOD1L1 (Q2311R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2521244	NM_148894.3(BOD1L1):c.6832G>A (p.Asp2278Asn)	BOD1L1 (D2278N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2546918	NM_148894.3(BOD1L1):c.6763A>G (p.Ile2255Val)	BOD1L1 (I2255V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2277189	NM_148894.3(BOD1L1):c.6739A>G (p.Met2247Val)	BOD1L1 (M2247V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2527103	NM_148894.3(BOD1L1):c.6691G>C (p.Val2231Leu)	BOD1L1 (V2231L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2321600	NM_148894.3(BOD1L1):c.6602C>T (p.Ala2201Val)	BOD1L1 (A2201V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2483417	NM_148894.3(BOD1L1):c.6582G>A (p.Met2194Ile)	BOD1L1 (M2194I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2350912	NM_148894.3(BOD1L1):c.6457G>A (p.Glu2153Lys)	BOD1L1 (E2153K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2360516	NM_148894.3(BOD1L1):c.6313A>G (p.Met2105Val)	BOD1L1 (M2105V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2612945	NM_148894.3(BOD1L1):c.6296T>G (p.Leu2099Arg)	BOD1L1 (L2099R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2464595	NM_148894.3(BOD1L1):c.6197A>C (p.Asn2066Thr)	BOD1L1 (N2066T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2614711	NM_148894.3(BOD1L1):c.6125A>G (p.Glu2042Gly)	BOD1L1 (E2042G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2304375	NM_148894.3(BOD1L1):c.6077C>G (p.Pro2026Arg)	BOD1L1 (P2026R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2305784	NM_148894.3(BOD1L1):c.6017G>T (p.Gly2006Val)	BOD1L1 (G2006V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2216478	NM_148894.3(BOD1L1):c.6005G>C (p.Gly2002Ala)	BOD1L1 (G2002A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2527546	NM_148894.3(BOD1L1):c.5891G>C (p.Gly1964Ala)	BOD1L1 (G1964A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2539415	NM_148894.3(BOD1L1):c.5885T>G (p.Val1962Gly)	BOD1L1 (V1962G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2411709	NM_148894.3(BOD1L1):c.5833G>C (p.Asp1945His)	BOD1L1 (D1945H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2237366	NM_148894.3(BOD1L1):c.5809A>G (p.Thr1937Ala)	BOD1L1 (T1937A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2263006	NM_148894.3(BOD1L1):c.5740C>T (p.His1914Tyr)	BOD1L1 (H1914Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2356372	NM_148894.3(BOD1L1):c.5689T>A (p.Leu1897Met)	BOD1L1 (L1897M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2223794	NM_148894.3(BOD1L1):c.5653A>C (p.Thr1885Pro)	BOD1L1 (T1885P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2328746	NM_148894.3(BOD1L1):c.5452A>T (p.Ile1818Leu)	BOD1L1 (I1818L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2531510	NM_148894.3(BOD1L1):c.5339C>T (p.Ser1780Phe)	BOD1L1 (S1780F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2271323	NM_148894.3(BOD1L1):c.5321G>A (p.Ser1774Asn)	BOD1L1 (S1774N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2373699	NM_148894.3(BOD1L1):c.5291A>G (p.Asp1764Gly)	BOD1L1 (D1764G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2595329	NM_148894.3(BOD1L1):c.5257C>T (p.Arg1753Cys)	BOD1L1 (R1753C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2468954	NM_148894.3(BOD1L1):c.5248C>T (p.Arg1750Trp)	BOD1L1 (R1750W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2546978	NM_148894.3(BOD1L1):c.5149A>C (p.Met1717Leu)	BOD1L1 (M1717L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2305247	NM_148894.3(BOD1L1):c.5091A>G (p.Ile1697Met)	BOD1L1 (I1697M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2388837	NM_148894.3(BOD1L1):c.5027G>A (p.Gly1676Glu)	BOD1L1 (G1676E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2271181	NM_148894.3(BOD1L1):c.4859T>C (p.Val1620Ala)	BOD1L1 (V1620A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2295056	NM_148894.3(BOD1L1):c.4846G>A (p.Gly1616Arg)	BOD1L1 (G1616R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2404136	NM_148894.3(BOD1L1):c.4801G>A (p.Ala1601Thr)	BOD1L1 (A1601T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2596257	NM_148894.3(BOD1L1):c.4619C>A (p.Thr1540Asn)	BOD1L1 (T1540N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2381525	NM_148894.3(BOD1L1):c.4606G>A (p.Gly1536Arg)	BOD1L1 (G1536R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2471619	NM_148894.3(BOD1L1):c.4517C>T (p.Ala1506Val)	BOD1L1 (A1506V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2220206	NM_148894.3(BOD1L1):c.4499G>A (p.Gly1500Glu)	BOD1L1 (G1500E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2390638	NM_148894.3(BOD1L1):c.4427G>C (p.Arg1476Thr)	BOD1L1 (R1476T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2319382	NM_148894.3(BOD1L1):c.4370T>C (p.Leu1457Pro)	BOD1L1 (L1457P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2464372	NM_148894.3(BOD1L1):c.4355C>A (p.Ala1452Asp)	BOD1L1 (A1452D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2613280	NM_148894.3(BOD1L1):c.4293G>T (p.Glu1431Asp)	BOD1L1 (E1431D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2379729	NM_148894.3(BOD1L1):c.4257G>C (p.Glu1419Asp)	BOD1L1 (E1419D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2400561	NM_148894.3(BOD1L1):c.4114G>C (p.Ala1372Pro)	BOD1L1 (A1372P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2488829	NM_148894.3(BOD1L1):c.4109A>C (p.His1370Pro)	BOD1L1 (H1370P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2240916	NM_148894.3(BOD1L1):c.4095C>A (p.His1365Gln)	BOD1L1 (H1365Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2210759	NM_148894.3(BOD1L1):c.4034A>G (p.Glu1345Gly)	BOD1L1 (E1345G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2405462	NM_148894.3(BOD1L1):c.3955C>T (p.Pro1319Ser)	BOD1L1 (P1319S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2377718	NM_148894.3(BOD1L1):c.3935G>A (p.Gly1312Asp)	BOD1L1 (G1312D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2517017	NM_148894.3(BOD1L1):c.3866T>C (p.Val1289Ala)	BOD1L1 (V1289A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2245378	NM_148894.3(BOD1L1):c.3625A>G (p.Ile1209Val)	BOD1L1 (I1209V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2242868	NM_148894.3(BOD1L1):c.3619A>G (p.Met1207Val)	BOD1L1 (M1207V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2535264	NM_148894.3(BOD1L1):c.3562G>A (p.Gly1188Arg)	BOD1L1 (G1188R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2469825	NM_148894.3(BOD1L1):c.3553C>T (p.Arg1185Cys)	BOD1L1 (R1185C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2492734	NM_148894.3(BOD1L1):c.3550G>C (p.Gly1184Arg)	BOD1L1 (G1184R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2310207	NM_148894.3(BOD1L1):c.3422G>A (p.Arg1141His)	BOD1L1 (R1141H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2245776	NM_148894.3(BOD1L1):c.3352G>C (p.Glu1118Gln)	BOD1L1 (E1118Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2302116	NM_148894.3(BOD1L1):c.3214G>A (p.Glu1072Lys)	BOD1L1 (E1072K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2247990	NM_148894.3(BOD1L1):c.3210G>T (p.Leu1070Phe)	BOD1L1 (L1070F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2211431	NM_148894.3(BOD1L1):c.3149G>A (p.Ser1050Asn)	BOD1L1 (S1050N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2320947	NM_148894.3(BOD1L1):c.2971A>G (p.Arg991Gly)	BOD1L1 (R991G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2570208	NM_148894.3(BOD1L1):c.2968C>T (p.His990Tyr)	BOD1L1 (H990Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2608324	NM_148894.3(BOD1L1):c.2947A>G (p.Ser983Gly)	BOD1L1 (S983G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign

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