"Ambry Genetics"[submitter] AND "NAV3"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3298530	NM_001024383.2(NAV3):c.77T>C (p.Ile26Thr)	NAV3 (I26T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338395	NM_001024383.2(NAV3):c.136G>C (p.Glu46Gln)	NAV3 (E46Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177383	NM_001024383.2(NAV3):c.139A>G (p.Thr47Ala)	NAV3 (T47A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523811	NM_001024383.2(NAV3):c.175A>C (p.Lys59Gln)	NAV3 (K59Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286235	NM_001024383.2(NAV3):c.194G>T (p.Gly65Val)	NAV3 (G65V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593286	NM_001024383.2(NAV3):c.232G>C (p.Glu78Gln)	NAV3 (E78Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177511	NM_001024383.2(NAV3):c.346A>G (p.Ile116Val)	LOC126861580, NAV3 (I116V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2327367	NM_001024383.2(NAV3):c.415A>T (p.Ile139Phe)	NAV3 (I139F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244893	NM_001024383.2(NAV3):c.595C>T (p.Leu199Phe)	NAV3 (L199F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291955	NM_001024383.2(NAV3):c.605G>A (p.Arg202Gln)	NAV3 (R202Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177613	NM_001024383.2(NAV3):c.620C>T (p.Ser207Phe)	NAV3 (S207F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177624	NM_001024383.2(NAV3):c.643G>A (p.Ala215Thr)	NAV3 (A215T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177649	NM_001024383.2(NAV3):c.763C>A (p.Pro255Thr)	NAV3 (P255T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271678	NM_001024383.2(NAV3):c.857A>G (p.Asn286Ser)	NAV3 (N286S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177652	NM_001024383.2(NAV3):c.862G>A (p.Ala288Thr)	NAV3 (A288T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349711	NM_001024383.2(NAV3):c.925G>A (p.Val309Met)	NAV3 (V309M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2539713	NM_001024383.2(NAV3):c.976C>G (p.Pro326Ala)	NAV3 (P326A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306208	NM_001024383.2(NAV3):c.980G>C (p.Ser327Thr)	NAV3 (S327T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205322	NM_001024383.2(NAV3):c.991C>A (p.Pro331Thr)	NAV3 (P331T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298529	NM_001024383.2(NAV3):c.1096C>A (p.Leu366Met)	NAV3 (L366M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177356	NM_001024383.2(NAV3):c.1132C>A (p.Pro378Thr)	NAV3 (P378T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458141	NM_001024383.2(NAV3):c.1178C>G (p.Ala393Gly)	NAV3 (A393G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484908	NM_001024383.2(NAV3):c.1181G>C (p.Arg394Pro)	NAV3 (R394P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228728	NM_001024383.2(NAV3):c.1196C>T (p.Pro399Leu)	NAV3 (P399L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2224582	NM_001024383.2(NAV3):c.1237G>A (p.Asp413Asn)	NAV3 (D413N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298544	NM_001024383.2(NAV3):c.1274G>A (p.Gly425Asp)	NAV3 (G425D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262756	NM_001024383.2(NAV3):c.1274G>C (p.Gly425Ala)	NAV3 (G425A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298547	NM_001024383.2(NAV3):c.1276T>G (p.Phe426Val)	NAV3 (F426V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333872	NM_001024383.2(NAV3):c.1373A>C (p.Asn458Thr)	NAV3 (N458T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177377	NM_001024383.2(NAV3):c.1396A>G (p.Lys466Glu)	NAV3 (K466E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177390	NM_001024383.2(NAV3):c.1461G>C (p.Glu487Asp)	NAV3 (E487D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466760	NM_001024383.2(NAV3):c.1502A>G (p.Lys501Arg)	NAV3 (K501R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360383	NM_001024383.2(NAV3):c.1514T>G (p.Leu505Trp)	NAV3 (L505W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558213	NM_001024383.2(NAV3):c.1621A>G (p.Ile541Val)	NAV3 (I541V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3177398	NM_001024383.2(NAV3):c.1637C>T (p.Thr546Ile)	NAV3 (T546I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378220	NM_001024383.2(NAV3):c.1742C>A (p.Ala581Asp)	NAV3 (A581D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525780	NM_001024383.2(NAV3):c.1747T>G (p.Leu583Val)	NAV3 (L583V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346539	NM_001024383.2(NAV3):c.1933G>A (p.Ala645Thr)	NAV3 (A645T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554840	NM_001024383.2(NAV3):c.1955G>A (p.Cys652Tyr)	NAV3 (C652Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292382	NM_001024383.2(NAV3):c.1961G>A (p.Ser654Asn)	NAV3 (S654N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222637	NM_001024383.2(NAV3):c.2074T>A (p.Leu692Met)	NAV3 (L692M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177428	NM_001024383.2(NAV3):c.2111G>A (p.Arg704His)	NAV3 (R704H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491056	NM_001024383.2(NAV3):c.2216C>G (p.Pro739Arg)	NAV3 (P739R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2294632	NM_001024383.2(NAV3):c.2258C>T (p.Ala753Val)	NAV3 (A753V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517674	NM_001024383.2(NAV3):c.2279G>A (p.Gly760Asp)	NAV3 (G760D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298538	NM_001024383.2(NAV3):c.2339T>C (p.Met780Thr)	NAV3 (M780T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177444	NM_001024383.2(NAV3):c.2405G>C (p.Ser802Thr)	NAV3 (S802T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298536	NM_001024383.2(NAV3):c.2509A>C (p.Asn837His)	NAV3 (N837H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280509	NM_001024383.2(NAV3):c.2539A>C (p.Asn847His)	NAV3 (N847H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298527	NM_001024383.2(NAV3):c.2545T>C (p.Tyr849His)	NAV3 (Y849H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274663	NM_001024383.2(NAV3):c.2564G>A (p.Arg855Gln)	NAV3 (R855Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508125	NM_001024383.2(NAV3):c.2588G>A (p.Arg863Gln)	NAV3 (R863Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400218	NM_001024383.2(NAV3):c.2614G>A (p.Asp872Asn)	NAV3 (D872N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615072	NM_001024383.2(NAV3):c.2753C>G (p.Ser918Cys)	NAV3 (S918C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517869	NM_001024383.2(NAV3):c.2792G>C (p.Arg931Pro)	NAV3 (R931P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309042	NM_001024383.2(NAV3):c.2801C>T (p.Thr934Ile)	NAV3 (T934I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607452	NM_001024383.2(NAV3):c.2828A>T (p.Glu943Val)	NAV3 (E943V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281888	NM_001024383.2(NAV3):c.2839C>A (p.Pro947Thr)	NAV3 (P947T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2474614	NM_001024383.2(NAV3):c.2942T>C (p.Leu981Pro)	NAV3 (L981P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177480	NM_001024383.2(NAV3):c.2956A>G (p.Thr986Ala)	NAV3 (T986A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395580	NM_001024383.2(NAV3):c.2988A>T (p.Gln996His)	NAV3 (Q996H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231310	NM_001024383.2(NAV3):c.3001T>C (p.Ser1001Pro)	NAV3 (S1001P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177488	NM_001024383.2(NAV3):c.3038C>A (p.Pro1013His)	NAV3 (P1013H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618010	NM_001024383.2(NAV3):c.3061G>A (p.Ala1021Thr)	NAV3 (A1021T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177494	NM_001024383.2(NAV3):c.3065C>A (p.Ser1022Tyr)	NAV3 (S1022Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602998	NM_001024383.2(NAV3):c.3104A>G (p.Gln1035Arg)	NAV3 (Q1035R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177503	NM_001024383.2(NAV3):c.3191C>A (p.Ser1064Tyr)	NAV3 (S1064Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177507	NM_001024383.2(NAV3):c.3196G>A (p.Gly1066Ser)	NAV3 (G1066S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298541	NM_001024383.2(NAV3):c.3215G>T (p.Gly1072Val)	NAV3 (G1072V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458074	NM_001024383.2(NAV3):c.3248G>C (p.Gly1083Ala)	NAV3 (G1083A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320218	NM_001024383.2(NAV3):c.3360G>C (p.Gln1120His)	NAV3 (Q1120H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177514	NM_001024383.2(NAV3):c.3517G>T (p.Ala1173Ser)	NAV3 (A1173S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177518	NM_001024383.2(NAV3):c.3523A>G (p.Thr1175Ala)	NAV3 (T1175A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257594	NM_001024383.2(NAV3):c.3530A>G (p.Lys1177Arg)	NAV3 (K1177R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373681	NM_001024383.2(NAV3):c.3563G>A (p.Arg1188His)	NAV3 (R1188H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373354	NM_001024383.2(NAV3):c.3608A>T (p.Lys1203Ile)	NAV3 (K1203I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177526	NM_001024383.2(NAV3):c.3709G>A (p.Gly1237Arg)	NAV3 (G1237R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298546	NM_001024383.2(NAV3):c.3728T>C (p.Ile1243Thr)	NAV3 (I1243T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298531	NM_001024383.2(NAV3):c.3841A>G (p.Thr1281Ala)	NAV3 (T1281A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2473669	NM_001024383.2(NAV3):c.3916G>A (p.Gly1306Ser)	NAV3 (G1306S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2471989	NM_001024383.2(NAV3):c.4063G>A (p.Ala1355Thr)	NAV3 (A1355T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546311	NM_001024383.2(NAV3):c.4265C>T (p.Pro1422Leu)	NAV3 (P1422L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474325	NM_001024383.2(NAV3):c.4286C>A (p.Thr1429Asn)	NAV3 (T1429N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177544	NM_001024383.2(NAV3):c.4307A>C (p.Asn1436Thr)	NAV3 (N1436T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2496565	NM_001024383.2(NAV3):c.4315G>C (p.Glu1439Gln)	NAV3 (E1439Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330352	NM_001024383.2(NAV3):c.4492C>T (p.Arg1498Cys)	NAV3 (R1498C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521546	NM_001024383.2(NAV3):c.4528G>A (p.Asp1510Asn)	NAV3 (D1510N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298542	NM_001024383.2(NAV3):c.4672C>G (p.Leu1558Val)	NAV3 (L1558V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298535	NM_001024383.2(NAV3):c.4681A>G (p.Thr1561Ala)	NAV3 (T1561A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298532	NM_001024383.2(NAV3):c.4850C>G (p.Thr1617Ser)	NAV3 (T1617S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177553	NM_001024383.2(NAV3):c.4882A>G (p.Ile1628Val)	NAV3 (I1628V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551275	NM_001024383.2(NAV3):c.4978A>G (p.Lys1660Glu)	NAV3 (K1660E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289934	NM_001024383.2(NAV3):c.5072C>A (p.Ala1691Asp)	NAV3 (A1691D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590950	NM_001024383.2(NAV3):c.5168C>A (p.Thr1723Asn)	NAV3 (T1723N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207215	NM_001024383.2(NAV3):c.5264C>T (p.Ser1755Leu)	NAV3 (S1755L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2496343	NM_001024383.2(NAV3):c.5281T>G (p.Ser1761Ala)	NAV3 (S1761A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258447	NM_001024383.2(NAV3):c.5291C>T (p.Ala1764Val)	NAV3 (A1764V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177571	NM_001024383.2(NAV3):c.5444C>T (p.Thr1815Met)	NAV3 (T1793M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177576	NM_001024383.2(NAV3):c.5495G>A (p.Arg1832Gln)	NAV3 (R1832Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298537	NM_001024383.2(NAV3):c.5507A>C (p.Asn1836Thr)	NAV3 (N1836T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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