ClinVar for Gene (Select 65268) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3190659	NM_006648.4(WNK2):c.872A>G (p.Lys291Arg)	WNK2 (K291R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190658	NM_006648.4(WNK2):c.6584C>T (p.Thr2195Met)	WNK2 (T2232M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190657	NM_006648.4(WNK2):c.6089G>A (p.Ser2030Asn)	WNK2 (S2030N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190656	NM_006648.4(WNK2):c.5908G>A (p.Val1970Met)	WNK2 (V1970M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190655	NM_006648.4(WNK2):c.5513A>G (p.Lys1838Arg)	WNK2 (K1838R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190654	NM_006648.4(WNK2):c.5474C>T (p.Ser1825Phe)	WNK2 (S1825F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190653	NM_006648.4(WNK2):c.5462A>G (p.Gln1821Arg)	WNK2 (Q1821R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190652	NM_006648.4(WNK2):c.5413G>A (p.Val1805Met)	WNK2 (V1805M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190651	NM_006648.4(WNK2):c.5333C>A (p.Ala1778Asp)	WNK2 (A1778D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190650	NM_006648.4(WNK2):c.5317G>A (p.Val1773Ile)	WNK2 (V1773I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190649	NM_006648.4(WNK2):c.5257A>C (p.Thr1753Pro)	WNK2 (T1790P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190648	NM_006648.4(WNK2):c.5221C>T (p.Pro1741Ser)	WNK2 (P1741S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190647	NM_006648.4(WNK2):c.512A>C (p.Asp171Ala)	WNK2 (D171A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190646	NM_006648.4(WNK2):c.5123T>C (p.Met1708Thr)	WNK2 (M1745T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190645	NM_006648.4(WNK2):c.5075A>T (p.Asp1692Val)	WNK2 (D1692V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190644	NM_006648.4(WNK2):c.5054G>A (p.Arg1685His)	WNK2 (R1722H +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3190643	NM_006648.4(WNK2):c.4880A>T (p.Glu1627Val)	WNK2 (E1664V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190642	NM_006648.4(WNK2):c.487C>T (p.Pro163Ser)	WNK2 (P163S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190641	NM_006648.4(WNK2):c.4780C>T (p.Arg1594Cys)	WNK2 (R1631C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190640	NM_006648.4(WNK2):c.451G>C (p.Val151Leu)	WNK2 (V151L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190639	NM_006648.4(WNK2):c.4490C>T (p.Ala1497Val)	WNK2 (A1497V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190638	NM_006648.4(WNK2):c.4379C>T (p.Pro1460Leu)	WNK2 (P1460L +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3190637	NM_006648.4(WNK2):c.4333G>T (p.Ala1445Ser)	WNK2 (A1445S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190636	NM_006648.4(WNK2):c.40C>G (p.Leu14Val)	WNK2 (L14V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190635	NM_006648.4(WNK2):c.3971C>T (p.Pro1324Leu)	WNK2 (P1324L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190634	NM_006648.4(WNK2):c.3721G>A (p.Ala1241Thr)	WNK2 (A1241T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190633	NM_006648.4(WNK2):c.3530C>T (p.Ala1177Val)	WNK2 (A1177V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190632	NM_006648.4(WNK2):c.3466G>A (p.Ala1156Thr)	WNK2 (A1156T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3190631	NM_006648.4(WNK2):c.3365A>G (p.Gln1122Arg)	WNK2 (Q1122R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190629	NM_006648.4(WNK2):c.2989G>A (p.Ala997Thr)	WNK2 (A997T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190628	NM_006648.4(WNK2):c.2642C>T (p.Pro881Leu)	WNK2 (P881L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190627	NM_006648.4(WNK2):c.2624C>T (p.Thr875Ile)	WNK2 (T875I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190625	NM_006648.4(WNK2):c.2434G>A (p.Gly812Ser)	WNK2 (G812S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3190624	NM_006648.4(WNK2):c.2360C>A (p.Pro787Gln)	WNK2 (P787Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190623	NM_006648.4(WNK2):c.2305G>A (p.Val769Met)	WNK2 (V769M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190622	NM_006648.4(WNK2):c.2282C>T (p.Pro761Leu)	WNK2 (P761L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190621	NM_006648.4(WNK2):c.2270C>T (p.Pro757Leu)	WNK2 (P757L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190620	NM_006648.4(WNK2):c.2078C>T (p.Pro693Leu)	WNK2 (P693L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190619	NM_006648.4(WNK2):c.1922C>A (p.Ala641Asp)	WNK2 (A641D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190618	NM_006648.4(WNK2):c.1910T>C (p.Leu637Pro)	WNK2 (L637P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190617	NM_006648.4(WNK2):c.1720C>A (p.Gln574Lys)	WNK2 (Q574K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3063071	GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020389)x3	ABCA1, ABCA2 +769 more	Copy number gain	not specified	GPathogenic
Select item 2671591	Single allele	CARD19, MIR24-1 +106 more	Deletion	not provided	GPathogenic
Select item 2659310	NM_006648.4(WNK2):c.3924C>T (p.Thr1308=)	WNK2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2659309	NM_006648.4(WNK2):c.3138G>C (p.Pro1046=)	WNK2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2618936	NM_006648.4(WNK2):c.2050G>A (p.Gly684Ser)	WNK2 (G684S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614042	NM_006648.4(WNK2):c.1610C>G (p.Ala537Gly)	WNK2 (A537G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2609418	NM_006648.4(WNK2):c.2924C>T (p.Pro975Leu)	WNK2 (P975L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602118	NM_006648.4(WNK2):c.1573G>A (p.Val525Ile)	WNK2 (V525I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598651	NM_006648.4(WNK2):c.4295C>T (p.Thr1432Met)	WNK2 (T1432M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593664	NM_006648.4(WNK2):c.2060C>T (p.Pro687Leu)	WNK2 (P687L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592410	NM_006648.4(WNK2):c.5702G>A (p.Arg1901Gln)	WNK2 (R1901Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590921	NM_006648.4(WNK2):c.4931T>C (p.Met1644Thr)	WNK2 (M1644T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569162	NM_006648.4(WNK2):c.4277T>C (p.Leu1426Pro)	WNK2 (L1426P +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2560773	NM_006648.4(WNK2):c.2068G>C (p.Ala690Pro)	WNK2 (A690P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554498	NM_006648.4(WNK2):c.5114C>T (p.Pro1705Leu)	WNK2 (P1742L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551341	NM_006648.4(WNK2):c.1790A>G (p.His597Arg)	WNK2 (H597R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546105	NM_006648.4(WNK2):c.3757G>A (p.Val1253Ile)	WNK2 (V1253I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543186	NM_006648.4(WNK2):c.2018A>G (p.Gln673Arg)	WNK2 (Q673R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541507	NM_006648.4(WNK2):c.3635A>G (p.Lys1212Arg)	WNK2 (K1212R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539535	NM_006648.4(WNK2):c.4549C>T (p.Pro1517Ser)	WNK2 (P1554S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536392	NM_006648.4(WNK2):c.407C>T (p.Ala136Val)	WNK2 (A136V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532627	NM_006648.4(WNK2):c.3313G>A (p.Ala1105Thr)	WNK2 (A1105T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524315	NM_006648.4(WNK2):c.531G>C (p.Glu177Asp)	WNK2 (E177D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518441	NM_006648.4(WNK2):c.2112G>C (p.Met704Ile)	WNK2 (M704I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515515	NM_006648.4(WNK2):c.1999C>G (p.Pro667Ala)	WNK2 (P667A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511330	NM_006648.4(WNK2):c.3983A>C (p.Glu1328Ala)	WNK2 (E1328A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510590	NM_006648.4(WNK2):c.349G>A (p.Glu117Lys)	WNK2 (E117K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492144	NM_006648.4(WNK2):c.3890A>G (p.Asn1297Ser)	WNK2 (N1297S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485893	NM_006648.4(WNK2):c.2208G>T (p.Gln736His)	WNK2 (Q736H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484453	NM_006648.4(WNK2):c.6523G>A (p.Ala2175Thr)	WNK2 (A2175T +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2481354	NM_006648.4(WNK2):c.2251C>G (p.Pro751Ala)	WNK2 (P751A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2479509	NM_006648.4(WNK2):c.6031C>A (p.Gln2011Lys)	WNK2 (Q2011K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468635	NM_006648.4(WNK2):c.3862G>A (p.Gly1288Arg)	WNK2 (G1288R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460717	NM_006648.4(WNK2):c.2337G>T (p.Gln779His)	WNK2 (Q779H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460247	NM_006648.4(WNK2):c.509G>C (p.Arg170Pro)	WNK2 (R170P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457921	NM_006648.4(WNK2):c.263G>T (p.Arg88Leu)	WNK2 (R88L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454970	NM_006648.4(WNK2):c.6106C>T (p.Arg2036Cys)	WNK2 (R2073C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409240	NM_006648.4(WNK2):c.5537G>A (p.Arg1846Lys)	WNK2 (R1846K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402540	NM_006648.4(WNK2):c.4291G>C (p.Glu1431Gln)	WNK2 (E1431Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401747	NM_006648.4(WNK2):c.2680G>A (p.Val894Met)	WNK2 (V894M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398398	NM_006648.4(WNK2):c.5347G>A (p.Asp1783Asn)	WNK2 (D1820N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395530	NM_006648.4(WNK2):c.5094A>T (p.Glu1698Asp)	WNK2 (E1735D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393381	NM_006648.4(WNK2):c.3014T>C (p.Leu1005Pro)	WNK2 (L1005P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390198	NM_006648.4(WNK2):c.2488C>A (p.Pro830Thr)	WNK2 (P830T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385739	NM_006648.4(WNK2):c.4496T>A (p.Leu1499Gln)	WNK2 (L1499Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383125	NM_006648.4(WNK2):c.2602C>T (p.Pro868Ser)	WNK2 (P868S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379830	NM_006648.4(WNK2):c.1931C>T (p.Ala644Val)	WNK2 (A644V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379081	NM_006648.4(WNK2):c.2105C>T (p.Pro702Leu)	WNK2 (P702L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377359	NM_006648.4(WNK2):c.4454A>G (p.His1485Arg)	WNK2 (H1485R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375699	NM_006648.4(WNK2):c.4888C>T (p.Pro1630Ser)	WNK2 (P1667S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373620	NM_006648.4(WNK2):c.4433C>G (p.Pro1478Arg)	WNK2 (P1478R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373266	NM_006648.4(WNK2):c.4438C>T (p.Pro1480Ser)	WNK2 (P1517S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366233	NM_006648.4(WNK2):c.260A>G (p.Glu87Gly)	WNK2 (E87G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364694	NM_006648.4(WNK2):c.1913G>A (p.Gly638Asp)	WNK2 (G638D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362913	NM_006648.4(WNK2):c.5456C>T (p.Pro1819Leu)	WNK2 (P1819L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357962	NM_006648.4(WNK2):c.6563C>T (p.Ala2188Val)	WNK2 (A2188V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352541	NM_006648.4(WNK2):c.2990C>T (p.Ala997Val)	WNK2 (A997V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346551	NM_006648.4(WNK2):c.1963C>G (p.Pro655Ala)	WNK2 (P655A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346232	NM_006648.4(WNK2):c.3124G>A (p.Val1042Met)	WNK2 (V1042M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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