ClinVar for Gene (Select 100133991) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3042528	NM_003954.5(MAP3K14):c.2289A>G (p.Ala763=)	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (synonymous variant)	MAP3K14-related condition	GLikely benign
Select item 3021485	NM_003954.5(MAP3K14):c.2094A>G (p.Pro698=)	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 3016933	NM_003954.5(MAP3K14):c.2434-7G>A	MAP3K14-AS1, LOC126862575 +1 more	Single nucleotide variant (intron variant)	NIK deficiency	GLikely benign
Select item 3006612	NM_003954.5(MAP3K14):c.2760C>T (p.Ile920=)	MAP3K14, MAP3K14-AS1	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 2991388	NM_003954.5(MAP3K14):c.2327-20T>C	MAP3K14, LOC126862575 +1 more	Single nucleotide variant (intron variant +1 more)	NIK deficiency	GLikely benign
Select item 2979361	NM_003954.5(MAP3K14):c.2193T>A (p.Thr731=)	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 2954702	NM_003954.5(MAP3K14):c.2028G>A (p.Pro676=)	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 2915820	NM_003954.5(MAP3K14):c.2184T>C (p.Pro728=)	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 2877214	NM_003954.5(MAP3K14):c.2727T>A (p.Val909=)	MAP3K14, MAP3K14-AS1	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 2838494	NM_003954.5(MAP3K14):c.2553C>G (p.Pro851=)	MAP3K14, MAP3K14-AS1	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 2803222	NM_003954.5(MAP3K14):c.2700C>T (p.Ser900=)	MAP3K14, MAP3K14-AS1	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 2768046	NM_003954.5(MAP3K14):c.2175C>T (p.Asn725=)	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 2766956	NM_003954.5(MAP3K14):c.2460G>T (p.Ser820=)	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 2747822	NM_003954.5(MAP3K14):c.2832G>A (p.Glu944=)	MAP3K14, MAP3K14-AS1	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 2699023	NM_003954.5(MAP3K14):c.2247G>A (p.Glu749=)	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 2695593	NM_003954.5(MAP3K14):c.2460G>A (p.Ser820=)	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 2694425	NM_003954.5(MAP3K14):c.2481C>T (p.Gly827=)	MAP3K14, MAP3K14-AS1	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 2628114	NM_003954.5(MAP3K14):c.2434-25C>T	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2620739	NM_152343.3(SPATA32):c.377C>A (p.Pro126Gln)	MAP3K14-AS1, SPATA32 (P126Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2608984	NM_003954.5(MAP3K14):c.2436C>A (p.Asn812Lys)	LOC126862575, MAP3K14 +1 more (N812K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2608525	NM_152343.3(SPATA32):c.776C>T (p.Pro259Leu)	MAP3K14-AS1, SPATA32 (P259L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2593223	NM_152343.3(SPATA32):c.334G>A (p.Val112Ile)	MAP3K14-AS1, SPATA32 (V112I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2548487	NM_152343.3(SPATA32):c.278C>T (p.Ser93Leu)	MAP3K14-AS1, SPATA32 (S93L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2534715	NM_152343.3(SPATA32):c.559C>G (p.Pro187Ala)	MAP3K14-AS1, SPATA32 (P187A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2455167	NM_152343.3(SPATA32):c.835C>T (p.Pro279Ser)	MAP3K14-AS1, SPATA32 (P279S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2407240	NM_003954.5(MAP3K14):c.2248C>G (p.Pro750Ala)	LOC126862575, MAP3K14 +1 more (P750A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2405749	NM_003954.5(MAP3K14):c.2555C>T (p.Thr852Ile)	MAP3K14, MAP3K14-AS1 (T852I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2399416	NM_152343.3(SPATA32):c.610G>A (p.Glu204Lys)	SPATA32, MAP3K14-AS1 (E204K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2394303	NM_152343.3(SPATA32):c.199G>A (p.Gly67Arg)	SPATA32, MAP3K14-AS1 (G67R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2366204	NM_152343.3(SPATA32):c.808C>G (p.Gln270Glu)	MAP3K14-AS1, SPATA32 (Q270E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2356450	NM_152343.3(SPATA32):c.50T>C (p.Val17Ala)	SPATA32, MAP3K14-AS1 (V17A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2352355	NM_152343.3(SPATA32):c.401G>A (p.Arg134Gln)	SPATA32, MAP3K14-AS1 (R134Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2300855	NM_152343.3(SPATA32):c.969C>A (p.Asp323Glu)	MAP3K14-AS1, SPATA32 (D323E)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2293641	NM_003954.5(MAP3K14):c.2146C>G (p.Pro716Ala)	LOC126862575, MAP3K14 +1 more (P716A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2251935	NM_003954.5(MAP3K14):c.2519C>T (p.Ser840Phe)	MAP3K14-AS1, MAP3K14 (S840F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2247957	NM_152343.3(SPATA32):c.294C>G (p.Asp98Glu)	SPATA32, MAP3K14-AS1 (D98E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2243290	NM_152343.3(SPATA32):c.640T>A (p.Ser214Thr)	SPATA32, MAP3K14-AS1 (S214T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2242633	NM_152343.3(SPATA32):c.157G>C (p.Asp53His)	SPATA32, MAP3K14-AS1 (D53H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2230765	NM_152343.3(SPATA32):c.844A>G (p.Thr282Ala)	SPATA32, MAP3K14-AS1 (T282A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2201003	NM_003954.5(MAP3K14):c.2288C>G (p.Ala763Gly)	LOC126862575, MAP3K14 +1 more (A763G)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 2182487	NM_003954.5(MAP3K14):c.2433+18C>T	MAP3K14-AS1, LOC126862575 +1 more	Single nucleotide variant (intron variant)	NIK deficiency	GLikely benign
Select item 2171574	NM_003954.5(MAP3K14):c.2437C>A (p.Pro813Thr)	LOC126862575, MAP3K14 +1 more (P813T)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 2149345	NM_003954.5(MAP3K14):c.2679+6G>T	MAP3K14, MAP3K14-AS1	Single nucleotide variant (intron variant)	NIK deficiency	GUncertain significance
Select item 2133367	NM_003954.5(MAP3K14):c.2823C>T (p.Gly941=)	MAP3K14, MAP3K14-AS1	Single nucleotide variant (synonymous variant)	NIK deficiency	GUncertain significance
Select item 2124249	NM_003954.5(MAP3K14):c.2326+20C>T	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (intron variant)	NIK deficiency	GUncertain significance
Select item 2122731	NM_003954.5(MAP3K14):c.2627G>A (p.Arg876Gln)	MAP3K14, MAP3K14-AS1 (R876Q)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 2105606	NM_003954.5(MAP3K14):c.2301G>T (p.Glu767Asp)	LOC126862575, MAP3K14 +1 more (E767D)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 2092486	NM_003954.5(MAP3K14):c.2183C>T (p.Pro728Leu)	LOC126862575, MAP3K14 +1 more (P728L)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 2088572	NM_003954.5(MAP3K14):c.2033A>G (p.Asn678Ser)	LOC126862575, MAP3K14 +1 more (N678S)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 2053995	NM_003954.5(MAP3K14):c.2387C>T (p.Ser796Leu)	LOC126862575, MAP3K14 +1 more (S796L)	Single nucleotide variant (non-coding transcript variant +1 more)	NIK deficiency	GUncertain significance
Select item 2041022	NM_003954.5(MAP3K14):c.2549G>A (p.Arg850Gln)	MAP3K14, MAP3K14-AS1 (R850Q)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 2038544	NM_003954.5(MAP3K14):c.2529C>T (p.Asn843=)	MAP3K14, MAP3K14-AS1	Single nucleotide variant (synonymous variant)	NIK deficiency	GUncertain significance
Select item 2024736	NM_003954.5(MAP3K14):c.2547dup (p.Arg850fs)	MAP3K14, MAP3K14-AS1 (R850fs)	Duplication (frameshift variant)	NIK deficiency	GUncertain significance
Select item 2006692	NM_003954.5(MAP3K14):c.2690C>G (p.Ala897Gly)	MAP3K14, MAP3K14-AS1 (A897G)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 1991306	NM_003954.5(MAP3K14):c.2576A>G (p.Asn859Ser)	MAP3K14, MAP3K14-AS1 (N859S)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 1990081	NM_003954.5(MAP3K14):c.2081C>T (p.Ser694Leu)	LOC126862575, MAP3K14 +1 more (S694L)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 1982163	NM_003954.5(MAP3K14):c.2482G>A (p.Val828Ile)	MAP3K14, MAP3K14-AS1 (V828I)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 1977587	NM_003954.5(MAP3K14):c.2327-20T>A	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	NIK deficiency	GLikely benign
Select item 1966015	NM_003954.5(MAP3K14):c.2433+16C>T	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (intron variant)	NIK deficiency	GUncertain significance
Select item 1901851	NM_003954.5(MAP3K14):c.2131C>T (p.Pro711Ser)	LOC126862575, MAP3K14 +1 more (P711S)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 1717522	NM_003954.5(MAP3K14):c.2722C>T (p.Pro908Ser)	MAP3K14, MAP3K14-AS1 (P908S)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 1672360	NM_003954.5(MAP3K14):c.2326+12C>T	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (intron variant)	NIK deficiency	GLikely benign
Select item 1668638	NM_003954.5(MAP3K14):c.2679+14G>A	MAP3K14, MAP3K14-AS1	Single nucleotide variant (intron variant)	NIK deficiency	GLikely benign
Select item 1663767	NM_003954.5(MAP3K14):c.2235G>A (p.Leu745=)	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 1653669	NM_003954.5(MAP3K14):c.2434-14T>C	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (intron variant)	NIK deficiency	GLikely benign
Select item 1653646	NM_003954.5(MAP3K14):c.2694C>T (p.Ala898=)	MAP3K14, MAP3K14-AS1	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 1635971	NM_003954.5(MAP3K14):c.2769G>A (p.Gln923=)	MAP3K14, MAP3K14-AS1	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 1612577	NM_003954.5(MAP3K14):c.1973-11C>A	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (intron variant)	NIK deficiency	GLikely benign
Select item 1610987	NM_003954.5(MAP3K14):c.2109T>G (p.Ala703=)	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 1607401	NM_003954.5(MAP3K14):c.2715C>T (p.Asp905=)	MAP3K14, MAP3K14-AS1	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 1600903	NM_003954.5(MAP3K14):c.2326+13G>A	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (intron variant)	NIK deficiency	GBenign
Select item 1596075	NM_003954.5(MAP3K14):c.2147C>G (p.Pro716Arg)	LOC126862575, MAP3K14 +1 more (P716R)	Single nucleotide variant (missense variant)	NIK deficiency	GLikely benign
Select item 1589190	NM_003954.5(MAP3K14):c.2679+17C>T	MAP3K14, MAP3K14-AS1	Single nucleotide variant (intron variant)	NIK deficiency	GBenign
Select item 1580497	NM_003954.5(MAP3K14):c.2433+8G>A	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (intron variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1575302	NM_003954.5(MAP3K14):c.2337C>T (p.Leu779=)	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	NIK deficiency	GLikely benign
Select item 1563296	NM_003954.5(MAP3K14):c.2461C>A (p.Arg821=)	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 1559245	NM_003954.5(MAP3K14):c.2502G>A (p.Gln834=)	MAP3K14, MAP3K14-AS1	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 1558378	NM_003954.5(MAP3K14):c.2679+11C>G	MAP3K14, MAP3K14-AS1	Single nucleotide variant (intron variant)	NIK deficiency	GLikely benign
Select item 1554822	NM_003954.5(MAP3K14):c.1973-11C>G	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (intron variant)	NIK deficiency	GLikely benign
Select item 1535829	NM_003954.5(MAP3K14):c.2826G>A (p.Gln942=)	MAP3K14, MAP3K14-AS1	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 1532734	NM_003954.5(MAP3K14):c.2796C>T (p.Phe932=)	MAP3K14, MAP3K14-AS1	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 1523257	NM_003954.5(MAP3K14):c.2116A>G (p.Thr706Ala)	LOC126862575, MAP3K14 +1 more (T706A)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 1522748	NM_003954.5(MAP3K14):c.1973-3T>C	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (intron variant)	NIK deficiency	GUncertain significance
Select item 1509452	NM_003954.5(MAP3K14):c.2797G>A (p.Ala933Thr)	MAP3K14, MAP3K14-AS1 (A933T)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 1508174	NM_003954.5(MAP3K14):c.2155C>T (p.Pro719Ser)	LOC126862575, MAP3K14 +1 more (P719S)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 1499094	NM_003954.5(MAP3K14):c.2326+5G>A	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (intron variant)	NIK deficiency	GUncertain significance
Select item 1495143	NM_003954.5(MAP3K14):c.2206G>C (p.Glu736Gln)	LOC126862575, MAP3K14 +1 more (E736Q)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 1480463	NM_003954.5(MAP3K14):c.2158G>T (p.Glu720Ter)	LOC126862575, MAP3K14 +1 more (E720*)	Single nucleotide variant (nonsense)	NIK deficiency	GUncertain significance
Select item 1457136	NM_003954.5(MAP3K14):c.2388G>A (p.Ser796=)	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	NIK deficiency	GLikely benign
Select item 1447736	NM_003954.5(MAP3K14):c.2167G>A (p.Glu723Lys)	LOC126862575, MAP3K14 +1 more (E723K)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 1437912	NM_003954.5(MAP3K14):c.2144C>G (p.Pro715Arg)	LOC126862575, MAP3K14 +1 more (P715R)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 1433823	NM_003954.5(MAP3K14):c.2530A>G (p.Met844Val)	MAP3K14, MAP3K14-AS1 (M844V)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 1428781	NM_003954.5(MAP3K14):c.2042A>G (p.Asn681Ser)	LOC126862575, MAP3K14 +1 more (N681S)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 1427660	NM_003954.5(MAP3K14):c.2639G>A (p.Arg880Gln)	MAP3K14, MAP3K14-AS1 (R880Q)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 1419904	NM_003954.5(MAP3K14):c.2446G>T (p.Ala816Ser)	LOC126862575, MAP3K14 +1 more (A816S)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 1419159	NM_003954.5(MAP3K14):c.2557G>A (p.Asp853Asn)	MAP3K14, MAP3K14-AS1 (D853N)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 1418729	NM_003954.5(MAP3K14):c.2470C>G (p.Leu824Val)	LOC126862575, MAP3K14 +1 more (L824V)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 1408688	NM_003954.5(MAP3K14):c.2144C>A (p.Pro715His)	LOC126862575, MAP3K14 +1 more (P715H)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 1396564	NM_003954.5(MAP3K14):c.2249C>G (p.Pro750Arg)	LOC126862575, MAP3K14 +1 more (P750R)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 1382233	NM_003954.5(MAP3K14):c.2180C>T (p.Ser727Phe)	LOC126862575, MAP3K14 +1 more (S727F)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance

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