"Invitae"[submitter] AND "MAP3K14"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 1535829	NM_003954.5(MAP3K14):c.2826G>A (p.Gln942=)	MAP3K14, MAP3K14-AS1	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
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 478060	NM_003954.5(MAP3K14):c.2820T>C (p.His940=)	MAP3K14, MAP3K14-AS1	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
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 1532734	NM_003954.5(MAP3K14):c.2796C>T (p.Phe932=)	MAP3K14, MAP3K14-AS1	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 1023728	NM_003954.5(MAP3K14):c.2783C>A (p.Pro928His)	MAP3K14, MAP3K14-AS1 (P928H)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 575207	NM_003954.5(MAP3K14):c.2779G>A (p.Ala927Thr)	MAP3K14, MAP3K14-AS1 (A927T)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
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 3006612	NM_003954.5(MAP3K14):c.2760C>T (p.Ile920=)	MAP3K14, MAP3K14-AS1	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 1132205	NM_003954.5(MAP3K14):c.2754G>A (p.Ser918=)	MAP3K14, MAP3K14-AS1	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 1081852	NM_003954.5(MAP3K14):c.2742G>A (p.Glu914=)	MAP3K14, MAP3K14-AS1	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 933453	NM_003954.5(MAP3K14):c.2729G>A (p.Arg910His)	MAP3K14, MAP3K14-AS1 (R910H)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 938219	NM_003954.5(MAP3K14):c.2728C>T (p.Arg910Cys)	MAP3K14, MAP3K14-AS1 (R910C)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
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 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 1607401	NM_003954.5(MAP3K14):c.2715C>T (p.Asp905=)	MAP3K14, MAP3K14-AS1	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 1170667	NM_003954.5(MAP3K14):c.2706C>G (p.Val902=)	MAP3K14, MAP3K14-AS1	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
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 1653646	NM_003954.5(MAP3K14):c.2694C>T (p.Ala898=)	MAP3K14, MAP3K14-AS1	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
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 1589190	NM_003954.5(MAP3K14):c.2679+17C>T	MAP3K14, MAP3K14-AS1	Single nucleotide variant (intron variant)	NIK deficiency	GBenign
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 1558378	NM_003954.5(MAP3K14):c.2679+11C>G	MAP3K14, MAP3K14-AS1	Single nucleotide variant (intron variant)	NIK deficiency	GLikely benign
Select item 758905	NM_003954.5(MAP3K14):c.2679+7G>A	MAP3K14, MAP3K14-AS1	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 640273	NM_003954.5(MAP3K14):c.2679+5G>A	MAP3K14, MAP3K14-AS1	Single nucleotide variant (intron variant)	NIK deficiency	GUncertain significance
Select item 659333	NM_003954.5(MAP3K14):c.2668A>G (p.Ile890Val)	MAP3K14, MAP3K14-AS1 (I890V)	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 745824	NM_003954.5(MAP3K14):c.2628G>A (p.Arg876=)	MAP3K14, MAP3K14-AS1	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
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 660828	NM_003954.5(MAP3K14):c.2615A>G (p.His872Arg)	MAP3K14, MAP3K14-AS1 (H872R)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 1015583	NM_003954.5(MAP3K14):c.2593A>G (p.Ile865Val)	MAP3K14, MAP3K14-AS1 (I865V)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 1153230	NM_003954.5(MAP3K14):c.2579-9G>A	MAP3K14, MAP3K14-AS1	Single nucleotide variant (intron variant)	NIK deficiency	GLikely benign
Select item 1091425	NM_003954.5(MAP3K14):c.2579-10C>T	MAP3K14, MAP3K14-AS1	Single nucleotide variant (intron variant)	NIK deficiency	GLikely benign
Select item 1151406	NM_003954.5(MAP3K14):c.2579-17C>T	MAP3K14-AS1, MAP3K14	Single nucleotide variant (intron variant)	NIK deficiency	GLikely benign
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 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 1097668	NM_003954.5(MAP3K14):c.2556C>T (p.Thr852=)	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 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 2024736	NM_003954.5(MAP3K14):c.2547dup (p.Arg850fs)	MAP3K14, MAP3K14-AS1 (R850fs)	Duplication (frameshift variant)	NIK deficiency	GUncertain significance
Select item 858282	NM_003954.5(MAP3K14):c.2548C>T (p.Arg850Trp)	MAP3K14, MAP3K14-AS1 (R850W)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 651083	NM_003954.5(MAP3K14):c.2543G>A (p.Arg848Gln)	MAP3K14, MAP3K14-AS1 (R848Q)	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 2038544	NM_003954.5(MAP3K14):c.2529C>T (p.Asn843=)	MAP3K14, MAP3K14-AS1	Single nucleotide variant (synonymous variant)	NIK deficiency	GUncertain significance
Select item 994378	NM_003954.5(MAP3K14):c.2520C>T (p.Ser840=)	MAP3K14, MAP3K14-AS1	Single nucleotide variant (synonymous variant)	NIK deficiency +1 more	GLikely benign
Select item 1143332	NM_003954.5(MAP3K14):c.2511T>C (p.Ala837=)	MAP3K14, MAP3K14-AS1	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 960379	NM_003954.5(MAP3K14):c.2485C>T (p.His829Tyr)	MAP3K14, MAP3K14-AS1 (H829Y)	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 2694425	NM_003954.5(MAP3K14):c.2481C>T (p.Gly827=)	MAP3K14, MAP3K14-AS1	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
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 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 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 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 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 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 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 544336	NM_003954.5(MAP3K14):c.2434-10G>A	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely 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 1102733	NM_003954.5(MAP3K14):c.2433+19C>T	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (intron 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 1966015	NM_003954.5(MAP3K14):c.2433+16C>T	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (intron variant)	NIK deficiency	GUncertain significance
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 574281	NM_003954.5(MAP3K14):c.2433+3G>A	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (intron variant)	NIK deficiency	GUncertain significance
Select item 796951	NM_003954.5(MAP3K14):c.2418G>C (p.Ser806=)	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 707986	NM_003954.5(MAP3K14):c.2418G>A (p.Ser806=)	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (synonymous variant)	NIK deficiency	GBenign
Select item 664708	NM_003954.5(MAP3K14):c.2405G>C (p.Ser802Thr)	LOC126862575, MAP3K14 +1 more (S802T)	Single nucleotide variant (non-coding transcript variant +1 more)	NIK deficiency	GUncertain significance
Select item 1113838	NM_003954.5(MAP3K14):c.2400C>T (p.Ile800=)	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	NIK deficiency	GLikely benign
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 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 797307	NM_003954.5(MAP3K14):c.2367G>A (p.Glu789=)	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	NIK deficiency	GLikely benign
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 1111402	NM_003954.5(MAP3K14):c.2331A>G (p.Leu777=)	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	NIK deficiency	GLikely benign
Select item 1105792	NM_003954.5(MAP3K14):c.2329T>C (p.Leu777=)	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	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 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 2124249	NM_003954.5(MAP3K14):c.2326+20C>T	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (intron variant)	NIK deficiency	GUncertain significance
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 1672360	NM_003954.5(MAP3K14):c.2326+12C>T	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (intron variant)	NIK deficiency	GLikely benign
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 859718	NM_003954.5(MAP3K14):c.2326+4C>T	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (intron variant)	NIK deficiency	GUncertain significance
Select item 1087832	NM_003954.5(MAP3K14):c.2313G>A (p.Gln771=)	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 544324	NM_003954.5(MAP3K14):c.2312A>C (p.Gln771Pro)	LOC126862575, MAP3K14 +1 more (Q771P)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 1145312	NM_003954.5(MAP3K14):c.2308C>T (p.Leu770=)	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
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 1147535	NM_003954.5(MAP3K14):c.2298G>A (p.Pro766=)	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1055934	NM_003954.5(MAP3K14):c.2293G>A (p.Val765Ile)	LOC126862575, MAP3K14 +1 more (V765I)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 544334	NM_003954.5(MAP3K14):c.2292C>T (p.Thr764=)	LOC126862575, MAP3K14 +1 more	Single nucleotide variant (synonymous variant)	NIK deficiency	GLikely benign
Select item 478059	NM_003954.5(MAP3K14):c.2290A>G (p.Thr764Ala)	LOC126862575, MAP3K14 +1 more (T764A)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
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 946492	NM_003954.5(MAP3K14):c.2282G>A (p.Arg761Gln)	MAP3K14, MAP3K14-AS1 +1 more (R761Q)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 1376558	NM_003954.5(MAP3K14):c.2281C>T (p.Arg761Trp)	MAP3K14-AS1, LOC126862575 +1 more (R761W)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
Select item 942501	NM_003954.5(MAP3K14):c.2266C>T (p.Pro756Ser)	LOC126862575, MAP3K14-AS1 +1 more (P756S)	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 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 862644	NM_003954.5(MAP3K14):c.2237C>T (p.Ser746Phe)	MAP3K14, MAP3K14-AS1 +1 more (S746F)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance
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 1495143	NM_003954.5(MAP3K14):c.2206G>C (p.Glu736Gln)	LOC126862575, MAP3K14 +1 more (E736Q)	Single nucleotide variant (missense variant)	NIK deficiency	GUncertain significance

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