DOCK1[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3273285	NM_001290223.2(DOCK1):c.149C>T (p.Thr50Met)	DOCK1 (T22M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2473646	NM_001290223.2(DOCK1):c.211A>G (p.Ile71Val)	DOCK1 (I43V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2482371	NM_001290223.2(DOCK1):c.286C>G (p.Leu96Val)	DOCK1 (L68V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3084899	NM_001290223.2(DOCK1):c.347G>A (p.Arg116Gln)	DOCK1 (R116Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2535530	NM_001290223.2(DOCK1):c.349A>G (p.Ser117Gly)	DOCK1 (S89G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3084902	NM_001290223.2(DOCK1):c.353T>G (p.Val118Gly)	DOCK1 (V118G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2337945	NM_001290223.2(DOCK1):c.356G>A (p.Arg119Gln)	DOCK1 (R119Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2541727	NM_001290223.2(DOCK1):c.377T>C (p.Ile126Thr)	DOCK1 (I126T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2275468	NM_001290223.2(DOCK1):c.386G>A (p.Arg129Gln)	DOCK1 (R129Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 521687	NM_001290223.2(DOCK1):c.436AAG[2] (p.Lys148del)	DOCK1 (K148del +2 more)	Microsatellite (inframe_deletion +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3273282	NM_001290223.2(DOCK1):c.526C>T (p.Pro176Ser)	DOCK1 (P188S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2542938	NM_001290223.2(DOCK1):c.577A>G (p.Lys193Glu)	DOCK1 (K205E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2279341	NM_001290223.2(DOCK1):c.640C>G (p.Gln214Glu)	DOCK1 (Q186E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3084913	NM_001290223.2(DOCK1):c.775T>C (p.Tyr259His)	DOCK1 (Y231H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3084890	NM_001290223.2(DOCK1):c.1187A>G (p.Asn396Ser)	DOCK1 (N347S +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3273281	NM_001290223.2(DOCK1):c.1651G>A (p.Ala551Thr)	DOCK1 (A266T +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278148	NM_001290223.2(DOCK1):c.1702G>A (p.Gly568Arg)	DOCK1 (G514R +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258907	NM_001290223.2(DOCK1):c.1819G>A (p.Gly607Ser)	DOCK1 (G553S +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558883	NM_001290223.2(DOCK1):c.1852A>G (p.Ile618Val)	DOCK1 (I546V +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084895	NM_001290223.2(DOCK1):c.1877C>T (p.Ser626Phe)	DOCK1 (S617F +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491434	NM_001290223.2(DOCK1):c.1880C>T (p.Thr627Met)	DOCK1 (T342M +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487454	NM_001290223.2(DOCK1):c.1986A>C (p.Lys662Asn)	DOCK1 (K590N +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273189	NM_001290223.2(DOCK1):c.2012T>A (p.Phe671Tyr)	DOCK1 (F662Y +7 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 521686	NM_001290223.2(DOCK1):c.2053dup (p.Glu685fs)	DOCK1 (E664fs +7 more)	Duplication (frameshift variant)	Inborn genetic diseases	GLikely pathogenic
Select item 2262914	NM_001290223.2(DOCK1):c.2214A>T (p.Lys738Asn)	DOCK1 (K666N +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2497728	NM_001290223.2(DOCK1):c.2249C>T (p.Pro750Leu)	DOCK1 (P465L +7 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3084896	NM_001290223.2(DOCK1):c.2261A>G (p.Glu754Gly)	DOCK1 (E705G +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602770	NM_001290223.2(DOCK1):c.2280G>A (p.Met760Ile)	DOCK1 (M739I +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554569	NM_001290223.2(DOCK1):c.2324T>A (p.Ile775Asn)	DOCK1 (I490N +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218314	NM_001290223.2(DOCK1):c.2333A>G (p.Asn778Ser)	DOCK1 (N769S +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2224441	NM_001290223.2(DOCK1):c.2401A>G (p.Asn801Asp)	DOCK1 (N516D +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2312804	NM_001290223.2(DOCK1):c.2430G>T (p.Gln810His)	DOCK1 (Q525H +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2312885	NM_001290223.2(DOCK1):c.2434G>A (p.Val812Ile)	DOCK1 (V770I +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2519457	NM_001290223.2(DOCK1):c.2521A>G (p.Met841Val)	DOCK1 (M751V +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332536	NM_001290223.2(DOCK1):c.2543A>G (p.Asn848Ser)	DOCK1 (N563S +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2640960	NM_001290223.2(DOCK1):c.2550C>T (p.Pro850=)	DOCK1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2608916	NM_001290223.2(DOCK1):c.2619G>T (p.Gln873His)	DOCK1 (Q852H +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2307363	NM_001290223.2(DOCK1):c.2740A>G (p.Arg914Gly)	DOCK1 (R842G +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623774	NM_001290223.2(DOCK1):c.2784G>A (p.Met928Ile)	DOCK1 (M856I +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1333365	NM_001290223.2(DOCK1):c.2791C>T (p.Leu931Phe)	DOCK1 (L646F +8 more)	Single nucleotide variant (missense variant)	DOCK1-related disorder	GUncertain significance
Select item 2613427	NM_001290223.2(DOCK1):c.2800A>C (p.Thr934Pro)	DOCK1 (T649P +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554325	NM_001290223.2(DOCK1):c.2826G>T (p.Met942Ile)	DOCK1 (M657I +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249051	NM_001290223.2(DOCK1):c.2833G>T (p.Asp945Tyr)	DOCK1 (D660Y +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482792	NM_001290223.2(DOCK1):c.2963A>C (p.Glu988Ala)	DOCK1 (E939A +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084898	NM_001290223.2(DOCK1):c.3001G>A (p.Val1001Ile)	DOCK1 (V959I +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268003	NM_001290223.2(DOCK1):c.3080T>C (p.Met1027Thr)	DOCK1 (M1027T +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339038	NM_001290223.2(DOCK1):c.3196A>G (p.Ser1066Gly)	DOCK1 (S1017G +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2688963	NM_001290223.2(DOCK1):c.3262A>T (p.Arg1088Ter)	DOCK1 (R1016* +8 more)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 2614754	NM_001290223.2(DOCK1):c.3269T>C (p.Met1090Thr)	DOCK1 (M1036T +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545206	NM_001290223.2(DOCK1):c.3353C>T (p.Thr1118Met)	DOCK1 (T1028M +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484740	NM_001290223.2(DOCK1):c.3456G>T (p.Lys1152Asn)	DOCK1 (K1103N +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084900	NM_001290223.2(DOCK1):c.3545A>G (p.Lys1182Arg)	DOCK1 (K1128R +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611013	NM_001290223.2(DOCK1):c.3583G>A (p.Val1195Ile)	DOCK1 (V1146I +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549072	NM_001290223.2(DOCK1):c.3600A>T (p.Glu1200Asp)	DOCK1 (E1151D +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411999	NM_001290223.2(DOCK1):c.3604C>T (p.Leu1202Phe)	DOCK1 (L1160F +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261622	NM_001290223.2(DOCK1):c.3649C>T (p.Arg1217Cys)	DOCK1 (R1217C +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3273277	NM_001290223.2(DOCK1):c.3756T>A (p.Asp1252Glu)	DOCK1 (D1162E +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084903	NM_001290223.2(DOCK1):c.3845G>A (p.Arg1282Gln)	DOCK1 (R1240Q +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2213909	NM_001290223.2(DOCK1):c.3950T>G (p.Leu1317Trp)	DOCK1 (L1227W +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2213910	NM_001290223.2(DOCK1):c.3951G>T (p.Leu1317Phe)	DOCK1 (L1032F +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2547585	NM_001290223.2(DOCK1):c.4019A>G (p.Lys1340Arg)	DOCK1 (K1250R +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2476939	NM_001290223.2(DOCK1):c.4019A>T (p.Lys1340Ile)	DOCK1 (K1268I +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2306740	NM_001290223.2(DOCK1):c.4048G>A (p.Val1350Ile)	DOCK1 (V1065I +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2316996	NM_001290223.2(DOCK1):c.4129G>C (p.Val1377Leu)	DOCK1 (V1287L +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084904	NM_001290223.2(DOCK1):c.4394G>A (p.Arg1465Gln)	DOCK1 (R1379Q +12 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2619036	NM_001290223.2(DOCK1):c.4407A>C (p.Lys1469Asn)	DOCK1 (K1420N +12 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334093	NM_001290223.2(DOCK1):c.4415A>G (p.Asp1472Gly)	DOCK1 (D1411G +12 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084905	NM_001290223.2(DOCK1):c.4609A>G (p.Ser1537Gly)	DOCK1 (S1476G +12 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2640961	NM_001290223.2(DOCK1):c.4644C>T (p.Asn1548=)	DOCK1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2292434	NM_001290223.2(DOCK1):c.4709G>A (p.Arg1570Gln)	DOCK1 (R1516Q +12 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286921	NM_001290223.2(DOCK1):c.4732G>T (p.Ala1578Ser)	DOCK1 (A1578S +12 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280350	NM_001290223.2(DOCK1):c.4761C>A (p.Asp1587Glu)	DOCK1 (D1302E +12 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520152	NM_001290223.2(DOCK1):c.4798A>G (p.Ile1600Val)	DOCK1 (I1514V +12 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615087	NM_001290223.2(DOCK1):c.4835G>A (p.Arg1612Lys)	DOCK1 (R1526K +12 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3273276	NM_001290223.2(DOCK1):c.4900G>A (p.Gly1634Ser)	DOCK1 (G1349S +12 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084906	NM_001290223.2(DOCK1):c.4903G>A (p.Val1635Ile)	DOCK1 (V1668I +12 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532215	NM_001290223.2(DOCK1):c.4946G>A (p.Arg1649His)	DOCK1 (R1577H +12 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084907	NM_001290223.2(DOCK1):c.5015C>T (p.Ser1672Phe)	DOCK1 (S1387F +12 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2681246	NM_001290223.2(DOCK1):c.5144A>G (p.Lys1715Arg)	DOCK1 (K1430R +12 more)	Single nucleotide variant (missense variant)	EBV-positive nodal T- and NK-cell lymphoma	GLikely benign
Select item 3084908	NM_001290223.2(DOCK1):c.5150A>G (p.Asp1717Gly)	DOCK1 (D1631G +12 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289258	NM_001290223.2(DOCK1):c.5285C>T (p.Pro1762Leu)	DOCK1 (P1690L +12 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296296	NM_001290223.2(DOCK1):c.5301G>A (p.Met1767Ile)	DOCK1 (M1677I +12 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3273280	NM_001290223.2(DOCK1):c.5323C>T (p.Arg1775Cys)	DOCK1 (R1490C +12 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3273284	NM_001290223.2(DOCK1):c.5345C>T (p.Ser1782Leu)	DOCK1 (S1692L +12 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225194	NM_001290223.2(DOCK1):c.5348C>T (p.Pro1783Leu)	DOCK1 (P1498L +12 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084909	NM_001290223.2(DOCK1):c.5368C>T (p.Pro1790Ser)	DOCK1 (P1700S +12 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3341711	NM_001290223.2(DOCK1):c.5427C>T (p.Asn1809=)	DOCK1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3084910	NM_001290223.2(DOCK1):c.5441C>T (p.Ala1814Val)	DOCK1 (A1724V +12 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2273921	NM_001290223.2(DOCK1):c.5446G>A (p.Val1816Met)	DOCK1 (V1730M +12 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332335	NM_001290223.2(DOCK1):c.5509G>A (p.Glu1837Lys)	DOCK1 (E1751K +12 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608093	NM_001290223.2(DOCK1):c.5623C>T (p.Arg1875Cys)	DOCK1 (R1826C +12 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2619770	NM_001290223.2(DOCK1):c.5624G>T (p.Arg1875Leu)	DOCK1 (R1590L +12 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491435	NM_001290223.2(DOCK1):c.5624G>A (p.Arg1875His)	DOCK1 (R1789H +12 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084911	NM_001290223.2(DOCK1):c.5636C>T (p.Ser1879Leu)	DOCK1 (S1818L +12 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553667	NM_001290223.2(DOCK1):c.5642A>G (p.Asp1881Gly)	DOCK1 (D1596G +12 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3273283	NM_001290223.2(DOCK1):c.5653G>T (p.Val1885Leu)	DOCK1 (V1824L +12 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332668	NM_001290223.2(DOCK1):c.5653G>A (p.Val1885Met)	DOCK1 (V1813M +12 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3063145	GRCh37/hg19 10q26.2(chr10:128766924-128900593)x1	DOCK1	Copy number loss	not specified	GUncertain significance
Select item 2685390	GRCh37/hg19 10q26.2(chr10:128785414-128920556)x1	DOCK1	Copy number loss	not provided	GUncertain significance
Select item 1809257	GRCh37/hg19 10q26.2(chr10:129048456-129091101)x1	DOCK1	Copy number loss	not provided	GUncertain significance

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