ClinVar for Gene (Select 9020) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3061708	NM_003954.5(MAP3K14):c.1647C>T (p.Ser549=)	MAP3K14	Single nucleotide variant (synonymous variant)	MAP3K14-related condition	GLikely benign
Select item 3052532	NM_003954.5(MAP3K14):c.1008C>T (p.Tyr336=)	MAP3K14	Single nucleotide variant (synonymous variant)	MAP3K14-related condition	GLikely benign
Select item 3049266	NM_003954.5(MAP3K14):c.1890C>G (p.Ile630Met)	MAP3K14 (I630M)	Single nucleotide variant (missense variant)	MAP3K14-related condition	GLikely benign
Select item 3046611	NM_003954.5(MAP3K14):c.816C>G (p.Leu272=)	MAP3K14	Single nucleotide variant (synonymous variant)	MAP3K14-related condition	GLikely benign
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 3022724	NM_003954.5(MAP3K14):c.816C>T (p.Leu272=)	MAP3K14	Single nucleotide variant (synonymous variant)	NIK deficiency	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 3014691	NM_003954.5(MAP3K14):c.538-10C>T	MAP3K14	Single nucleotide variant (intron variant)	NIK deficiency	GLikely benign
Select item 3011390	NM_003954.5(MAP3K14):c.579C>T (p.Thr193=)	MAP3K14	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 3007279	NM_003954.5(MAP3K14):c.735C>G (p.Pro245=)	MAP3K14	Single nucleotide variant (synonymous 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 3000670	NM_003954.5(MAP3K14):c.1553-11C>T	MAP3K14	Single nucleotide variant (intron variant)	NIK deficiency	GLikely benign
Select item 2994046	NM_003954.5(MAP3K14):c.1658-9C>T	MAP3K14	Single nucleotide variant (intron 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 2986583	NM_003954.5(MAP3K14):c.652C>T (p.Arg218Trp)	MAP3K14 (R218W)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 2985828	NM_003954.5(MAP3K14):c.538-17T>A	MAP3K14	Single nucleotide variant (intron variant)	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 2976571	NM_003954.5(MAP3K14):c.1180C>A (p.Arg394=)	MAP3K14	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 2918771	NM_003954.5(MAP3K14):c.1066C>T (p.Leu356=)	MAP3K14	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 2918077	NM_003954.5(MAP3K14):c.1443C>G (p.Val481=)	MAP3K14	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 2915245	NM_003954.5(MAP3K14):c.1707G>T (p.Leu569=)	MAP3K14	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 2910825	NM_003954.5(MAP3K14):c.1839G>A (p.Pro613=)	MAP3K14	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 2909910	NM_003954.5(MAP3K14):c.90G>A (p.Pro30=)	MAP3K14	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 2896718	NM_003954.5(MAP3K14):c.561C>A (p.Ala187=)	MAP3K14	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 2895420	NM_003954.5(MAP3K14):c.714C>T (p.His238=)	MAP3K14	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 2886726	NM_003954.5(MAP3K14):c.747C>G (p.Gly249=)	MAP3K14	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 2885351	NM_003954.5(MAP3K14):c.1569G>A (p.Leu523=)	MAP3K14	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 2883722	NM_003954.5(MAP3K14):c.861G>T (p.Leu287=)	MAP3K14	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 2877159	NM_003954.5(MAP3K14):c.1875C>G (p.Leu625=)	MAP3K14	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 2875268	NM_003954.5(MAP3K14):c.538-13T>C	MAP3K14	Single nucleotide variant (intron variant)	NIK deficiency	GLikely benign
Select item 2863717	NM_003954.5(MAP3K14):c.546G>A (p.Glu182=)	MAP3K14	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 2858798	NM_003954.5(MAP3K14):c.1250T>A (p.Met417Lys)	MAP3K14 (M417K)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 2856728	NM_003954.5(MAP3K14):c.537+16C>T	MAP3K14	Single nucleotide variant (intron 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 2806971	NM_003954.5(MAP3K14):c.1761G>T (p.Leu587=)	MAP3K14	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 2779008	NM_003954.5(MAP3K14):c.24C>T (p.Cys8=)	MAP3K14	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 2769132	NM_003954.5(MAP3K14):c.997G>A (p.Val333Met)	MAP3K14 (V333M)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 2768531	NM_003954.5(MAP3K14):c.1902G>A (p.Leu634=)	MAP3K14	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 2728920	NM_003954.5(MAP3K14):c.1421-15C>T	MAP3K14	Single nucleotide variant (intron variant)	NIK deficiency	GLikely benign
Select item 2725428	NM_003954.5(MAP3K14):c.885C>T (p.Pro295=)	MAP3K14	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 2723959	NM_003954.5(MAP3K14):c.1002G>A (p.Glu334=)	MAP3K14	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 2723811	NM_003954.5(MAP3K14):c.213C>T (p.Ser71=)	MAP3K14	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 2721526	NM_003954.5(MAP3K14):c.1134G>A (p.Glu378=)	MAP3K14	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 2712601	NM_003954.5(MAP3K14):c.477G>C (p.Val159=)	MAP3K14	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 2711582	NM_003954.5(MAP3K14):c.538-8C>G	MAP3K14	Single nucleotide variant (intron variant)	NIK deficiency	GLikely benign
Select item 2709718	NM_003954.5(MAP3K14):c.1658-12C>A	MAP3K14	Single nucleotide variant (intron 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 2694717	NM_003954.5(MAP3K14):c.1467G>A (p.Glu489=)	MAP3K14	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 2628305	NM_003954.5(MAP3K14):c.1291-89G>A	MAP3K14	Single nucleotide variant (intron variant)	not specified	GBenign
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 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 2428361	NM_003954.5(MAP3K14):c.1102C>T (p.Arg368Trp)	MAP3K14 (R368W)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 2421883	NM_003954.5(MAP3K14):c.1858C>T (p.Pro620Ser)	MAP3K14 (P620S)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 2421069	NM_003954.5(MAP3K14):c.609A>G (p.Pro203=)	MAP3K14	Single nucleotide variant (synonymous variant)	NIK deficiency	GUncertain significance
Select item 2414030	NM_003954.5(MAP3K14):c.1935G>A (p.Ala645=)	MAP3K14	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
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 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 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 2197378	NM_003954.5(MAP3K14):c.215A>C (p.Glu72Ala)	MAP3K14 (E72A)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 2194213	NM_003954.5(MAP3K14):c.89C>T (p.Pro30Leu)	MAP3K14 (P30L)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 2190813	NM_003954.5(MAP3K14):c.1575C>T (p.Ser525=)	MAP3K14	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
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 2165774	NM_003954.5(MAP3K14):c.41C>T (p.Ser14Leu)	MAP3K14 (S14L)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 2159451	NM_003954.5(MAP3K14):c.836C>T (p.Pro279Leu)	MAP3K14 (P279L)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 2154698	NM_003954.5(MAP3K14):c.1958G>A (p.Arg653Gln)	MAP3K14 (R653Q)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 2153234	NM_003954.5(MAP3K14):c.1821+9C>T	MAP3K14	Single nucleotide variant (intron variant)	NIK deficiency	GLikely benign
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 2147537	NM_003954.5(MAP3K14):c.1802G>A (p.Arg601Gln)	MAP3K14 (R601Q)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 2144280	NM_003954.5(MAP3K14):c.1602C>T (p.Asp534=)	MAP3K14	Single nucleotide variant (synonymous variant)	NIK deficiency	GUncertain significance
Select item 2142273	NM_003954.5(MAP3K14):c.1337G>A (p.Gly446Glu)	MAP3K14 (G446E)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 2140782	NM_003954.5(MAP3K14):c.735C>T (p.Pro245=)	MAP3K14	Single nucleotide variant (synonymous variant)	NIK deficiency	GUncertain significance
Select item 2139080	NM_003954.5(MAP3K14):c.428G>A (p.Arg143Gln)	MAP3K14 (R143Q)	Single nucleotide variant (missense 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 2132715	NM_003954.5(MAP3K14):c.1735G>A (p.Val579Ile)	MAP3K14 (V579I)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 2130459	NM_003954.5(MAP3K14):c.1708G>T (p.Gly570Cys)	MAP3K14 (G570C)	Single nucleotide variant (missense 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 2121097	NM_003954.5(MAP3K14):c.1821G>A (p.Lys607=)	MAP3K14	Single nucleotide variant (synonymous variant)	NIK deficiency	GUncertain significance
Select item 2120544	NM_003954.5(MAP3K14):c.1048G>C (p.Ala350Pro)	MAP3K14 (A350P)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 2118981	NM_003954.5(MAP3K14):c.1152+4A>G	MAP3K14	Single nucleotide variant (intron variant)	NIK deficiency	GUncertain significance
Select item 2117894	NM_003954.5(MAP3K14):c.200C>A (p.Ala67Asp)	MAP3K14 (A67D)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 2114431	NM_003954.5(MAP3K14):c.458C>A (p.Ser153Tyr)	MAP3K14 (S153Y)	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 2090063	NM_003954.5(MAP3K14):c.1797C>A (p.Phe599Leu)	MAP3K14 (F599L)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 2088911	NM_003954.5(MAP3K14):c.1152+12C>T	MAP3K14	Single nucleotide variant (intron variant)	NIK deficiency	GLikely benign
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

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