ClinVar for Gene (Select 7409) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3188275	NM_005428.4(VAV1):c.2068G>A (p.Asp690Asn)	VAV1 (D690N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188273	NM_005428.4(VAV1):c.1693G>A (p.Gly565Ser)	VAV1 (G565S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188272	NM_005428.4(VAV1):c.1408A>G (p.Met470Val)	VAV1 (M438V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3020384	NM_005428.4(VAV1):c.1643G>A (p.Arg548Gln)	VAV1 (R516Q +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3014163	NM_005428.4(VAV1):c.655-4G>A	VAV1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3010596	NM_005428.4(VAV1):c.1140G>C (p.Leu380=)	VAV1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3010303	NM_005428.4(VAV1):c.1998G>C (p.Leu666=)	VAV1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3010159	NM_005428.4(VAV1):c.264C>G (p.Leu88=)	VAV1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3009899	NM_005428.4(VAV1):c.1104G>A (p.Gln368=)	VAV1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3009425	NM_005428.4(VAV1):c.2332+18G>C	VAV1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3007160	NM_005428.4(VAV1):c.805G>A (p.Val269Ile)	VAV1 (V237I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3006348	NM_005428.4(VAV1):c.1398+16C>T	VAV1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3005852	NM_005428.4(VAV1):c.1771G>A (p.Glu591Lys)	VAV1 (E559K +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3004481	NM_005428.4(VAV1):c.666G>A (p.Lys222=)	VAV1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3002902	NM_005428.4(VAV1):c.786C>T (p.Gly262=)	VAV1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3001348	NM_005428.4(VAV1):c.71C>T (p.Thr24Ile)	VAV1 (T24I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3000891	NM_005428.4(VAV1):c.2047A>G (p.Ser683Gly)	VAV1 (S651G +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2999606	NM_005428.4(VAV1):c.952G>A (p.Gly318Arg)	VAV1 (G286R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2999038	NM_005428.4(VAV1):c.1977C>T (p.Val659=)	VAV1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2998839	NM_005428.4(VAV1):c.2217+16C>T	VAV1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2996029	NM_005428.4(VAV1):c.2218-5T>A	VAV1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2994478	NM_005428.4(VAV1):c.2095G>T (p.Val699Leu)	VAV1 (V699L +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2993558	NM_005428.4(VAV1):c.654+4G>A	VAV1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2991243	NM_005428.4(VAV1):c.2060A>G (p.Asn687Ser)	VAV1 (N687S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2991194	NM_005428.4(VAV1):c.1265+18G>A	VAV1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2987404	NM_005428.4(VAV1):c.1015C>A (p.Leu339Ile)	VAV1 (L307I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2983916	NM_005428.4(VAV1):c.2369G>A (p.Arg790His)	VAV1 (R758H +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2983349	NM_005428.4(VAV1):c.1815G>A (p.Gly605=)	VAV1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2979343	NM_005428.4(VAV1):c.556C>A (p.Pro186Thr)	VAV1 (P186T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2978519	NM_005428.4(VAV1):c.1024-16G>C	VAV1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2977086	NM_005428.4(VAV1):c.2013-4G>A	VAV1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2977009	NM_005428.4(VAV1):c.204+16G>A	VAV1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2975631	NM_005428.4(VAV1):c.516G>A (p.Glu172=)	VAV1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2974477	NM_005428.4(VAV1):c.2130-19G>A	VAV1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2973629	NM_005428.4(VAV1):c.1620C>T (p.Phe540=)	VAV1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2972923	NM_005428.4(VAV1):c.827+15G>A	VAV1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2971523	NM_005428.4(VAV1):c.1825C>A (p.Pro609Thr)	VAV1 (P609T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2969587	NM_005428.4(VAV1):c.1509-6T>G	VAV1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2969466	NM_005428.4(VAV1):c.2493G>C (p.Trp831Cys)	VAV1 (W831C +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2967983	NM_005428.4(VAV1):c.1179+11G>A	VAV1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2967239	NM_005428.4(VAV1):c.81G>T (p.Gly27=)	VAV1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2966806	NM_005428.4(VAV1):c.655-3C>T	VAV1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2966732	NM_005428.4(VAV1):c.33C>T (p.Leu11=)	VAV1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2965574	NM_005428.4(VAV1):c.1855C>T (p.Leu619Phe)	VAV1 (L619F +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2960608	NM_005428.4(VAV1):c.205-11T>A	VAV1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2959883	NM_005428.4(VAV1):c.540G>A (p.Ser180=)	VAV1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2959812	NM_005428.4(VAV1):c.2485-17T>G	VAV1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2959388	NM_005428.4(VAV1):c.559-9C>T	VAV1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2958825	NM_005428.4(VAV1):c.828-15G>A	VAV1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2957977	NM_005428.4(VAV1):c.1933A>C (p.Asn645His)	VAV1 (N613H +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2957374	NM_005428.4(VAV1):c.676C>T (p.Arg226Trp)	VAV1 (R226W +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2957003	NM_005428.4(VAV1):c.451G>A (p.Asp151Asn)	VAV1 (D151N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2954745	NM_005428.4(VAV1):c.1610+12G>A	VAV1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2909394	NM_005428.4(VAV1):c.927+6C>T	VAV1	Single nucleotide variant (intron variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2908253	NM_005428.4(VAV1):c.1539C>T (p.Ala513=)	VAV1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2907688	NM_005428.4(VAV1):c.852C>T (p.Cys284=)	VAV1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2906834	NM_005428.4(VAV1):c.1708+5G>T	VAV1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2906581	NM_005428.4(VAV1):c.649C>A (p.Gln217Lys)	VAV1 (Q217K)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2904313	NM_005428.4(VAV1):c.2113T>C (p.Phe705Leu)	VAV1 (F673L +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2902526	NM_005428.4(VAV1):c.1884G>A (p.Thr628=)	VAV1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2902504	NM_005428.4(VAV1):c.2017G>T (p.Ala673Ser)	VAV1 (A641S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2901750	NM_005428.4(VAV1):c.1828C>G (p.Pro610Ala)	VAV1 (P610A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2900110	NM_005428.4(VAV1):c.1246C>A (p.Arg416=)	VAV1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2899119	NM_005428.4(VAV1):c.1826C>T (p.Pro609Leu)	VAV1 (P577L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2898846	NM_005428.4(VAV1):c.2148G>A (p.Lys716=)	VAV1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2894932	NM_005428.4(VAV1):c.827+6A>C	VAV1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2892967	NM_005428.4(VAV1):c.258C>T (p.Phe86=)	VAV1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2890936	NM_005428.4(VAV1):c.891G>A (p.Val297=)	VAV1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2889788	NM_005428.4(VAV1):c.1137A>G (p.Thr379=)	VAV1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2888626	NM_005428.4(VAV1):c.1587C>T (p.Cys529=)	VAV1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2887744	NM_005428.4(VAV1):c.2455G>A (p.Gly819Ser)	VAV1 (G787S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2887031	NM_005428.4(VAV1):c.667C>G (p.Pro223Ala)	VAV1 (P223A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2885772	NM_005428.4(VAV1):c.1508+9C>A	VAV1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2885318	NM_005428.4(VAV1):c.2129+6T>G	VAV1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2881556	NM_005428.4(VAV1):c.321+13C>T	VAV1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2880487	NM_005428.4(VAV1):c.1683C>G (p.Val561=)	VAV1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2880486	NM_005428.4(VAV1):c.136C>T (p.Leu46=)	VAV1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2879066	NM_005428.4(VAV1):c.1568T>C (p.Phe523Ser)	VAV1 (F491S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2875932	NM_005428.4(VAV1):c.2152A>G (p.Ile718Val)	VAV1 (I696V +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2868450	NM_005428.4(VAV1):c.1203C>T (p.Gly401=)	VAV1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2868154	NM_005428.4(VAV1):c.205-16C>A	VAV1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2867306	NM_005428.4(VAV1):c.1794G>A (p.Glu598=)	VAV1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2865311	NM_005428.4(VAV1):c.2508C>T (p.Tyr836=)	VAV1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2861311	NM_005428.4(VAV1):c.2212del (p.Thr739fs)	VAV1 (T707fs +2 more)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 2861283	NM_005428.4(VAV1):c.2218-18A>T	VAV1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2848890	NM_005428.4(VAV1):c.1785del (p.Lys596fs)	VAV1 (K564fs +1 more)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 2844968	NM_005428.4(VAV1):c.415G>A (p.Glu139Lys)	VAV1 (E139K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2841849	NM_005428.4(VAV1):c.2013-16T>C	VAV1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2839232	NM_005428.4(VAV1):c.828-15_828-13del	VAV1	Deletion (intron variant)	not provided	GLikely benign
Select item 2833782	NM_005428.4(VAV1):c.2013-6T>C	VAV1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2830229	NM_005428.4(VAV1):c.827+9C>T	VAV1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2826104	NM_005428.4(VAV1):c.928-6C>T	VAV1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2814419	NM_005428.4(VAV1):c.601G>A (p.Glu201Lys)	VAV1 (E201K)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2811360	NM_005428.4(VAV1):c.654+13C>T	VAV1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2807015	NM_005428.4(VAV1):c.1093-13G>A	VAV1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2806281	NM_005428.4(VAV1):c.1756G>A (p.Asp586Asn)	VAV1 (D554N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2805997	NM_005428.4(VAV1):c.654+16C>T	VAV1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2801119	NM_005428.4(VAV1):c.1509C>T (p.Ile503=)	VAV1	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 2800651	NM_005428.4(VAV1):c.1718G>T (p.Gly573Val)	VAV1 (G573V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2794269	NM_005428.4(VAV1):c.378C>T (p.Ile126=)	VAV1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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