ClinVar for Gene (Select 89797) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3177339	NM_145117.5(NAV2):c.914C>T (p.Pro305Leu)	LOC126861157, NAV2 (P241L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177328	NM_145117.5(NAV2):c.787G>A (p.Ala263Thr)	LOC126861157, NAV2 (A199T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177318	NM_145117.5(NAV2):c.7090G>A (p.Asp2364Asn)	NAV2 (D2364N +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177310	NM_145117.5(NAV2):c.685G>T (p.Val229Leu)	NAV2 (V165L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177293	NM_145117.5(NAV2):c.6587G>T (p.Gly2196Val)	NAV2 (G1260V +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177289	NM_145117.5(NAV2):c.6580A>G (p.Ile2194Val)	NAV2 (I1258V +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177287	NM_145117.5(NAV2):c.6491T>C (p.Val2164Ala)	NAV2 (V2100A +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177282	NM_145117.5(NAV2):c.6490G>A (p.Val2164Ile)	NAV2 (V1228I +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177277	NM_145117.5(NAV2):c.647C>G (p.Ala216Gly)	NAV2 (A216G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177273	NM_145117.5(NAV2):c.646G>A (p.Ala216Thr)	NAV2 (A152T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177258	NM_145117.5(NAV2):c.625G>A (p.Ala209Thr)	NAV2 (A145T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177239	NM_145117.5(NAV2):c.5536A>G (p.Met1846Val)	NAV2 (M1849V +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177237	NM_145117.5(NAV2):c.5506G>A (p.Glu1836Lys)	NAV2 (E1836K +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177225	NM_145117.5(NAV2):c.5492A>G (p.Asn1831Ser)	NAV2 (N1834S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177224	NM_145117.5(NAV2):c.5462C>A (p.Ser1821Tyr)	NAV2 (S1824Y +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177201	NM_145117.5(NAV2):c.5285A>C (p.Asn1762Thr)	NAV2 (N1818T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177179	NM_145117.5(NAV2):c.4869G>A (p.Ser1623=)	NAV2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3177170	NM_145117.5(NAV2):c.4741G>T (p.Asp1581Tyr)	NAV2 (D1517Y +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177159	NM_145117.5(NAV2):c.4712A>G (p.Asn1571Ser)	NAV2 (N1594S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177146	NM_145117.5(NAV2):c.4600G>A (p.Val1534Met)	NAV2 (V1470M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177135	NM_145117.5(NAV2):c.4505G>A (p.Arg1502His)	NAV2 (R1438H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177128	NM_145117.5(NAV2):c.4246A>G (p.Ile1416Val)	LOC126861158, NAV2 +1 more (I502V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3177116	NM_145117.5(NAV2):c.3922A>G (p.Thr1308Ala)	LOC126861158, NAV2 +1 more (T394A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177106	NM_145117.5(NAV2):c.3815C>T (p.Pro1272Leu)	NAV2, NAV2-AS2 (P1272L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177102	NM_145117.5(NAV2):c.3800C>T (p.Ser1267Leu)	NAV2, NAV2-AS2 (S1290L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177085	NM_145117.5(NAV2):c.3554G>A (p.Arg1185Gln)	NAV2, NAV2-AS2 (R1121Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177076	NM_145117.5(NAV2):c.3475G>A (p.Val1159Ile)	NAV2, NAV2-AS2 (V1095I +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3177057	NM_145117.5(NAV2):c.31A>G (p.Lys11Glu)	LEISA1, NAV2 (K11E)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3177050	NM_145117.5(NAV2):c.3178G>A (p.Ala1060Thr)	NAV2, NAV2-AS2 (A1083T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3177040	NM_145117.5(NAV2):c.3029G>A (p.Arg1010Gln)	NAV2, NAV2-AS2 (R1010Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3177037	NM_145117.5(NAV2):c.3026G>T (p.Arg1009Met)	NAV2, NAV2-AS2 (R945M +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3177034	NM_145117.5(NAV2):c.2998A>G (p.Ile1000Val)	NAV2, NAV2-AS2 (I1000V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3177029	NM_145117.5(NAV2):c.2939G>A (p.Arg980Lys)	NAV2, NAV2-AS2 (R66K +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3177020	NM_145117.5(NAV2):c.2741C>A (p.Thr914Asn)	NAV2 (T914N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177017	NM_145117.5(NAV2):c.2735G>A (p.Arg912Gln)	NAV2 (R912Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3177012	NM_145117.5(NAV2):c.2642G>A (p.Ser881Asn)	NAV2 (S817N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176994	NM_145117.5(NAV2):c.2398A>G (p.Met800Val)	NAV2 (M736V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176983	NM_145117.5(NAV2):c.2270C>T (p.Thr757Met)	NAV2 (T693M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176970	NM_145117.5(NAV2):c.197T>A (p.Leu66Gln)	LEISA1, NAV2 (L66Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3176965	NM_145117.5(NAV2):c.1855T>C (p.Ser619Pro)	NAV2 (S619P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176962	NM_145117.5(NAV2):c.1853C>A (p.Ser618Tyr)	NAV2 (S641Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176943	NM_145117.5(NAV2):c.1715T>G (p.Met572Arg)	NAV2 (M595R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176920	NM_145117.5(NAV2):c.151A>T (p.Thr51Ser)	LEISA1, NAV2 (T51S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3176914	NM_145117.5(NAV2):c.1411T>C (p.Phe471Leu)	NAV2 (F471L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176902	NM_145117.5(NAV2):c.128G>A (p.Ser43Asn)	LEISA1, NAV2 (S43N)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3176888	NM_145117.5(NAV2):c.1118T>C (p.Met373Thr)	NAV2 (M309T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176881	NM_145117.5(NAV2):c.1046C>G (p.Pro349Arg)	NAV2 (P285R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3060888	NM_145117.5(NAV2):c.5505A>C (p.Ser1835=)	NAV2	Single nucleotide variant (synonymous variant)	NAV2-related condition	GBenign
Select item 3060247	NM_145117.5(NAV2):c.3054G>T (p.Glu1018Asp)	NAV2, NAV2-AS2 (E1018D +3 more)	Single nucleotide variant (missense variant +1 more)	NAV2-related condition	GBenign
Select item 3059216	NM_145117.5(NAV2):c.1404G>C (p.Gln468His)	NAV2 (Q404H +2 more)	Single nucleotide variant (missense variant)	NAV2-related condition	GBenign
Select item 3058864	NM_145117.5(NAV2):c.326G>A (p.Arg109Lys)	NAV2 (R109K +1 more)	Single nucleotide variant (missense variant)	NAV2-related condition	GBenign
Select item 3058727	NM_145117.5(NAV2):c.1267C>T (p.Arg423Trp)	NAV2 (R359W +2 more)	Single nucleotide variant (missense variant)	NAV2-related condition	GLikely benign
Select item 3056585	NM_145117.5(NAV2):c.4885-7T>C	NAV2	Single nucleotide variant (intron variant)	NAV2-related condition	GBenign
Select item 3056539	NM_145117.5(NAV2):c.6187G>A (p.Ala2063Thr)	NAV2 (A1127T +4 more)	Single nucleotide variant (missense variant)	NAV2-related condition	GBenign
Select item 3056515	NM_145117.5(NAV2):c.6943G>A (p.Val2315Ile)	NAV2 (V1379I +4 more)	Single nucleotide variant (missense variant)	NAV2-related condition	GBenign
Select item 3055960	NM_145117.5(NAV2):c.2768+9G>A	NAV2	Single nucleotide variant (intron variant)	NAV2-related condition	GBenign
Select item 3051618	NM_145117.5(NAV2):c.51C>G (p.Pro17=)	LEISA1, NAV2	Single nucleotide variant (synonymous variant +2 more)	NAV2-related condition	GBenign
Select item 3051424	NM_145117.5(NAV2):c.4070G>A (p.Ser1357Asn)	LOC126861158, NAV2 +1 more (S1293N +3 more)	Single nucleotide variant (missense variant)	NAV2-related condition	GLikely benign
Select item 3050828	NM_145117.5(NAV2):c.5022C>T (p.Asn1674=)	NAV2	Single nucleotide variant (synonymous variant)	NAV2-related condition	GLikely benign
Select item 3049908	NM_145117.5(NAV2):c.5917-8A>G	NAV2	Single nucleotide variant (intron variant)	NAV2-related condition	GBenign
Select item 3049690	NM_145117.5(NAV2):c.5007A>G (p.Glu1669=)	NAV2	Single nucleotide variant (synonymous variant)	NAV2-related condition	GBenign
Select item 3043993	NM_145117.5(NAV2):c.6424C>T (p.Arg2142Cys)	NAV2 (R1206C +4 more)	Single nucleotide variant (missense variant)	NAV2-related condition	GLikely benign
Select item 3043956	NM_145117.5(NAV2):c.1880C>G (p.Thr627Ser)	NAV2 (T563S +2 more)	Single nucleotide variant (missense variant)	NAV2-related condition	GBenign
Select item 3042577	NM_145117.5(NAV2):c.4356C>T (p.Thr1452=)	LOC126861158, NAV2 +1 more	Single nucleotide variant (synonymous variant +1 more)	NAV2-related condition	GLikely benign
Select item 3042293	NM_145117.5(NAV2):c.1617T>C (p.Ile539=)	NAV2	Single nucleotide variant (synonymous variant)	NAV2-related condition	GBenign
Select item 3042260	NM_145117.5(NAV2):c.2292G>A (p.Thr764=)	NAV2	Single nucleotide variant (synonymous variant)	NAV2-related condition	GBenign
Select item 3042132	NM_145117.5(NAV2):c.3391G>A (p.Gly1131Ser)	NAV2, NAV2-AS2 (G1067S +3 more)	Single nucleotide variant (missense variant)	NAV2-related condition	GBenign
Select item 3042108	NM_145117.5(NAV2):c.155A>G (p.Tyr52Cys)	LEISA1, NAV2 (Y52C)	Single nucleotide variant (missense variant +2 more)	NAV2-related condition	GLikely benign
Select item 3040987	NM_145117.5(NAV2):c.170C>G (p.Pro57Arg)	LEISA1, NAV2 (P57R)	Single nucleotide variant (missense variant +2 more)	NAV2-related condition	GBenign
Select item 3040230	NM_145117.5(NAV2):c.5767A>G (p.Met1923Val)	NAV2 (M1859V +4 more)	Single nucleotide variant (missense variant)	NAV2-related condition	GBenign
Select item 3039323	NM_145117.5(NAV2):c.84C>A (p.Pro28=)	LEISA1, NAV2	Single nucleotide variant (synonymous variant +2 more)	NAV2-related condition	GBenign
Select item 3038580	NM_145117.5(NAV2):c.3384C>T (p.Ser1128=)	NAV2, NAV2-AS2	Single nucleotide variant (synonymous variant)	NAV2-related condition	GLikely benign
Select item 3037978	NM_145117.5(NAV2):c.5934C>G (p.Leu1978=)	NAV2	Single nucleotide variant (synonymous variant)	NAV2-related condition	GBenign
Select item 3037721	NM_145117.5(NAV2):c.4297A>G (p.Ile1433Val)	LOC126861158, NAV2 +1 more (I1369V +3 more)	Single nucleotide variant (missense variant +1 more)	NAV2-related condition	GBenign
Select item 3037451	NM_145117.5(NAV2):c.1532C>T (p.Thr511Met)	NAV2 (T447M +2 more)	Single nucleotide variant (missense variant)	NAV2-related condition	GBenign
Select item 3037161	NM_145117.5(NAV2):c.2051A>C (p.Glu684Ala)	NAV2 (E620A +2 more)	Single nucleotide variant (missense variant)	NAV2-related condition	GLikely benign
Select item 3035227	NM_145117.5(NAV2):c.5934C>A (p.Leu1978=)	NAV2	Single nucleotide variant (synonymous variant)	NAV2-related condition	GLikely benign
Select item 3034257	NM_145117.5(NAV2):c.985G>C (p.Ala329Pro)	NAV2 (A265P +2 more)	Single nucleotide variant (missense variant)	NAV2-related condition	GLikely benign
Select item 3033902	NM_145117.5(NAV2):c.6112G>A (p.Glu2038Lys)	NAV2 (E1102K +4 more)	Single nucleotide variant (missense variant)	NAV2-related condition	GLikely benign
Select item 3033377	NM_145117.5(NAV2):c.1762C>T (p.Arg588Trp)	NAV2 (R524W +2 more)	Single nucleotide variant (missense variant)	NAV2-related condition	GLikely benign
Select item 3031350	NM_145117.5(NAV2):c.4769C>T (p.Ser1590Phe)	NAV2 (S1526F +3 more)	Single nucleotide variant (missense variant)	NAV2-related condition	GUncertain significance
Select item 2689535	NM_145117.5(NAV2):c.5377G>A (p.Ala1793Thr)	NAV2 (A1729T +4 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2689534	NM_145117.5(NAV2):c.5209C>T (p.Arg1737Cys)	NAV2 (R1673C +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2689533	NM_145117.5(NAV2):c.1454A>G (p.Asn485Ser)	NAV2 (N421S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2689532	NM_145117.5(NAV2):c.2389G>A (p.Ala797Thr)	NAV2 (A733T +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2689531	NM_145117.5(NAV2):c.2713G>A (p.Val905Met)	NAV2 (V841M +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2689530	NM_145117.5(NAV2):c.26A>C (p.Lys9Thr)	LEISA1, NAV2 (K9T)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2689529	NM_145117.5(NAV2):c.2821C>T (p.Leu941Phe)	NAV2 (L27F +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2689528	NM_145117.5(NAV2):c.6098G>A (p.Arg2033His)	NAV2 (R1097H +4 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2689527	NM_145117.5(NAV2):c.4714G>T (p.Ala1572Ser)	NAV2 (A1508S +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2641684	NM_145117.5(NAV2):c.6418-7A>G	NAV2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2641683	NM_145117.5(NAV2):c.5953G>C (p.Gly1985Arg)	NAV2 (G1049R +4 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2641682	NM_145117.5(NAV2):c.4884A>C (p.Thr1628=)	NAV2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2641681	NM_145117.5(NAV2):c.3156G>A (p.Thr1052=)	NAV2, NAV2-AS2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2641680	NM_145117.5(NAV2):c.2698C>T (p.Pro900Ser)	NAV2 (P836S +2 more)	Single nucleotide variant (missense variant)	NAV2-related condition +1 more	GLikely benign
Select item 2641679	NM_145117.5(NAV2):c.2319C>T (p.Ser773=)	NAV2	Single nucleotide variant (synonymous variant)	NAV2-related condition +1 more	GBenign/Likely benign
Select item 2641678	NM_145117.5(NAV2):c.1320G>A (p.Glu440=)	NAV2	Single nucleotide variant (synonymous variant)	NAV2-related condition +1 more	GBenign/Likely benign
Select item 2641677	NM_145117.5(NAV2):c.333C>T (p.Leu111=)	NAV2	Single nucleotide variant (synonymous variant)	NAV2-related condition +1 more	GBenign/Likely benign
Select item 2641676	NM_145117.5(NAV2):c.39A>C (p.Gly13=)	LEISA1, NAV2	Single nucleotide variant (synonymous variant +2 more)	NAV2-related condition +1 more	GLikely benign
Select item 2635428	NM_145117.5(NAV2):c.4742A>G (p.Asp1581Gly)	NAV2 (D1517G +3 more)	Single nucleotide variant (missense variant)	NAV2-related condition	GUncertain significance

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