ClinVar for Gene (Select 51776) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3380851	NM_016653.3(MAP3K20):c.499G>A (p.Val167Ile)	MAP3K20 (V167I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3344197	NM_016653.3(MAP3K20):c.1410A>G (p.Ile470Met)	MAP3K20, MAP3K20-AS1 (I470M)	Single nucleotide variant (missense variant)	MAP3K20-related disorder	GUncertain significance
Select item 3338527	NM_016653.3(MAP3K20):c.159+28133C>G	MAP3K20	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 3247568	NC_000002.11:g.(?_173420879)_(174232392_?)del	CDCA7, MAP3K20 +2 more	Deletion	not provided	GPathogenic
Select item 3062617	GRCh37/hg19 2q24.2-31.1(chr2:162692199-174452488)x1	ABCB11, B3GALT1 +57 more	Copy number loss	not specified	GPathogenic
Select item 3059052	NM_016653.3(MAP3K20):c.987+3977G>A	MAP3K20, MAP3K20-AS1	Single nucleotide variant (synonymous variant +1 more)	MAP3K20-related disorder	GLikely benign
Select item 3046499	NM_016653.3(MAP3K20):c.-9C>T	MAP3K20	Single nucleotide variant (5 prime UTR variant)	MAP3K20-related disorder	GLikely benign
Select item 3034647	NM_016653.3(MAP3K20):c.987+4224GAT[6]	MAP3K20, MAP3K20-AS1	Microsatellite (intron variant)	MAP3K20-related disorder	GLikely benign
Select item 3022009	NM_016653.3(MAP3K20):c.248-17C>T	MAP3K20	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3015747	NM_016653.3(MAP3K20):c.1026C>T (p.Asp342=)	MAP3K20, MAP3K20-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3008550	NM_016653.3(MAP3K20):c.918G>A (p.Gln306=)	MAP3K20, MAP3K20-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3006147	NM_016653.3(MAP3K20):c.1703-14C>A	MAP3K20, MAP3K20-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3005200	NM_016653.3(MAP3K20):c.1703-9C>A	MAP3K20, MAP3K20-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3003365	NM_016653.3(MAP3K20):c.160-4A>G	MAP3K20	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2998241	NM_016653.3(MAP3K20):c.416-12_416-11del	MAP3K20	Deletion (intron variant)	not provided	GLikely benign
Select item 2996679	NM_016653.3(MAP3K20):c.159+13C>T	MAP3K20	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2995336	NM_016653.3(MAP3K20):c.588C>T (p.Leu196=)	MAP3K20, MAP3K20-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2995286	NM_016653.3(MAP3K20):c.415+20A>C	MAP3K20	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2992871	NM_016653.3(MAP3K20):c.1360-15T>C	MAP3K20, MAP3K20-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2992543	NM_016653.3(MAP3K20):c.867A>T (p.Ala289=)	MAP3K20, MAP3K20-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2986717	NM_016653.3(MAP3K20):c.416-16T>C	MAP3K20	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2986581	NM_016653.3(MAP3K20):c.445-19C>T	MAP3K20	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2985166	NM_016653.3(MAP3K20):c.1593G>A (p.Ser531=)	MAP3K20, MAP3K20-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2981640	NM_016653.3(MAP3K20):c.234T>C (p.Tyr78=)	MAP3K20	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2970272	NM_016653.3(MAP3K20):c.1404T>C (p.Ile468=)	MAP3K20, MAP3K20-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2965529	NM_016653.3(MAP3K20):c.583-11T>G	MAP3K20, MAP3K20-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2965379	NM_016653.3(MAP3K20):c.669+9A>G	MAP3K20, MAP3K20-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2965292	NM_016653.3(MAP3K20):c.852-20C>T	MAP3K20, MAP3K20-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2964843	NM_016653.3(MAP3K20):c.1702+16C>T	MAP3K20, MAP3K20-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2960554	NM_016653.3(MAP3K20):c.270C>G (p.Leu90=)	MAP3K20	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2956098	NM_016653.3(MAP3K20):c.1089A>G (p.Val363=)	MAP3K20, MAP3K20-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2955058	NM_016653.3(MAP3K20):c.1005G>A (p.Glu335=)	MAP3K20, MAP3K20-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2916996	NM_016653.3(MAP3K20):c.600A>G (p.Leu200=)	MAP3K20, MAP3K20-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2914209	NM_016653.3(MAP3K20):c.1849C>A (p.Arg617=)	MAP3K20, MAP3K20-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2906046	NM_016653.3(MAP3K20):c.2065A>G (p.Asn689Asp)	MAP3K20, MAP3K20-AS1 (N689D)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2894144	NM_016653.3(MAP3K20):c.1770T>C (p.Arg590=)	MAP3K20, MAP3K20-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2886662	NM_016653.3(MAP3K20):c.1218A>G (p.Lys406=)	MAP3K20, MAP3K20-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2881668	NM_016653.3(MAP3K20):c.1703-15C>A	MAP3K20, MAP3K20-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2879478	NM_016653.3(MAP3K20):c.1148A>G (p.Glu383Gly)	MAP3K20, MAP3K20-AS1 (E383G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2877134	NM_016653.3(MAP3K20):c.1296G>A (p.Glu432=)	MAP3K20, MAP3K20-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2868419	NM_016653.3(MAP3K20):c.882A>G (p.Leu294=)	MAP3K20, MAP3K20-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2844282	NM_016653.3(MAP3K20):c.444+13C>A	MAP3K20	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2825831	NM_016653.3(MAP3K20):c.464C>T (p.Ser155Phe)	MAP3K20 (S155F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2818147	NM_016653.3(MAP3K20):c.432T>C (p.Asp144=)	MAP3K20	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2813489	NM_016653.3(MAP3K20):c.408A>C (p.Ser136=)	MAP3K20	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2813030	NM_016653.3(MAP3K20):c.736G>A (p.Asp246Asn)	MAP3K20, MAP3K20-AS1 (D246N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2806162	NM_016653.3(MAP3K20):c.583-4C>A	MAP3K20, MAP3K20-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2799538	NM_016653.3(MAP3K20):c.1560T>C (p.Val520=)	MAP3K20, MAP3K20-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2793390	NM_016653.3(MAP3K20):c.744+18T>C	MAP3K20, MAP3K20-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2785355	NM_016653.3(MAP3K20):c.744+11G>A	MAP3K20, MAP3K20-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2784518	NM_016653.3(MAP3K20):c.1632A>G (p.Lys544=)	MAP3K20, MAP3K20-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2781353	NM_016653.3(MAP3K20):c.1360-9T>A	MAP3K20, MAP3K20-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2777134	NM_016653.3(MAP3K20):c.2283C>T (p.Ser761=)	MAP3K20, MAP3K20-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2770680	NM_016653.3(MAP3K20):c.1267-14G>A	MAP3K20, MAP3K20-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2739729	NM_016653.3(MAP3K20):c.416-5T>C	MAP3K20	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2729421	NM_016653.3(MAP3K20):c.1821C>T (p.Gly607=)	MAP3K20, MAP3K20-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2720000	NM_016653.3(MAP3K20):c.1545A>G (p.Thr515=)	MAP3K20, MAP3K20-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2695259	NM_016653.3(MAP3K20):c.549_550del (p.Ser184fs)	MAP3K20 (S184fs)	Microsatellite (frameshift variant)	not provided	GPathogenic
Select item 2651546	NM_016653.3(MAP3K20):c.987+4003G>A	MAP3K20, MAP3K20-AS1 (S364N)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2424739	NC_000002.11:g.(?_171675102)_(174232392_?)dup	CDCA7, CYBRD1 +15 more	Duplication	not provided	GUncertain significance
Select item 2420710	NM_016653.3(MAP3K20):c.967A>T (p.Thr323Ser)	MAP3K20, MAP3K20-AS1 (T323S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2416284	NM_016653.3(MAP3K20):c.2270G>C (p.Ser757Thr)	MAP3K20, MAP3K20-AS1 (S757T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2414943	NM_016653.3(MAP3K20):c.2347G>A (p.Ala783Thr)	MAP3K20, MAP3K20-AS1 (A783T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2413770	NM_016653.3(MAP3K20):c.1997C>A (p.Thr666Asn)	MAP3K20, MAP3K20-AS1 (T666N)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2413754	NM_016653.3(MAP3K20):c.719A>C (p.His240Pro)	MAP3K20, MAP3K20-AS1 (H240P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2236453	NM_016653.3(MAP3K20):c.664A>G (p.Asn222Asp)	MAP3K20, MAP3K20-AS1 (N222D)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2201302	NM_016653.3(MAP3K20):c.752C>G (p.Pro251Arg)	MAP3K20, MAP3K20-AS1 (P251R)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 2195587	NM_016653.3(MAP3K20):c.2145C>T (p.Tyr715=)	MAP3K20, MAP3K20-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2193389	NM_016653.3(MAP3K20):c.670-4G>A	MAP3K20, MAP3K20-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2187352	NM_016653.3(MAP3K20):c.1740G>A (p.Arg580=)	MAP3K20, MAP3K20-AS1	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 2183772	NM_016653.3(MAP3K20):c.1020G>A (p.Thr340=)	MAP3K20, MAP3K20-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2175202	NM_016653.3(MAP3K20):c.1629G>T (p.Val543=)	MAP3K20, MAP3K20-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2175065	NM_016653.3(MAP3K20):c.2340A>G (p.Pro780=)	MAP3K20, MAP3K20-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2174881	NM_016653.3(MAP3K20):c.1214A>G (p.Glu405Gly)	MAP3K20, MAP3K20-AS1 (E405G)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2172812	NM_016653.3(MAP3K20):c.948G>A (p.Lys316=)	MAP3K20, MAP3K20-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2172069	NM_016653.3(MAP3K20):c.905G>A (p.Ser302Asn)	MAP3K20, MAP3K20-AS1 (S302N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2161200	NM_016653.3(MAP3K20):c.1143G>A (p.Leu381=)	MAP3K20, MAP3K20-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2153428	NM_016653.3(MAP3K20):c.2242T>C (p.Leu748=)	MAP3K20, MAP3K20-AS1	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 2149538	NM_016653.3(MAP3K20):c.988-3C>T	MAP3K20, MAP3K20-AS1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2146920	NM_016653.3(MAP3K20):c.1952A>G (p.His651Arg)	MAP3K20, MAP3K20-AS1 (H651R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2146581	NM_016653.3(MAP3K20):c.1164C>G (p.Asp388Glu)	MAP3K20, MAP3K20-AS1 (D388E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2144452	NM_016653.3(MAP3K20):c.2048G>A (p.Arg683His)	MAP3K20, MAP3K20-AS1 (R683H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2135391	NM_016653.3(MAP3K20):c.1552-15del	MAP3K20, MAP3K20-AS1	Deletion (intron variant)	not provided	GUncertain significance
Select item 2133244	NM_016653.3(MAP3K20):c.299A>C (p.Glu100Ala)	MAP3K20 (E100A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2109759	NM_016653.3(MAP3K20):c.1992T>G (p.Thr664=)	MAP3K20, MAP3K20-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2108739	NM_016653.3(MAP3K20):c.1702+7dup	MAP3K20, MAP3K20-AS1	Duplication (intron variant)	not provided	GUncertain significance
Select item 2105146	NM_016653.3(MAP3K20):c.1601G>A (p.Trp534Ter)	MAP3K20, MAP3K20-AS1 (W534*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2102279	NM_016653.3(MAP3K20):c.1203+16A>C	MAP3K20, MAP3K20-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2100553	NM_016653.3(MAP3K20):c.2368G>T (p.Ala790Ser)	MAP3K20, MAP3K20-AS1 (A790S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2093259	NM_016653.3(MAP3K20):c.852-14C>G	MAP3K20, MAP3K20-AS1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2082518	NM_016653.3(MAP3K20):c.2181G>A (p.Ser727=)	MAP3K20, MAP3K20-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2076985	NM_016653.3(MAP3K20):c.582+20_582+22del	MAP3K20	Deletion (intron variant)	not provided	GUncertain significance
Select item 2068266	NM_016653.3(MAP3K20):c.1812C>T (p.His604=)	MAP3K20, MAP3K20-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2054769	NM_016653.3(MAP3K20):c.862G>A (p.Glu288Lys)	MAP3K20, MAP3K20-AS1 (E288K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2049162	NM_016653.3(MAP3K20):c.71G>C (p.Gly24Ala)	MAP3K20 (G24A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2049066	NM_016653.3(MAP3K20):c.1087G>A (p.Val363Ile)	MAP3K20, MAP3K20-AS1 (V363I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2046804	NM_016653.3(MAP3K20):c.2384G>A (p.Arg795His)	MAP3K20, MAP3K20-AS1 (R795H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2042007	NM_016653.3(MAP3K20):c.282T>G (p.Ile94Met)	MAP3K20 (I94M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2041562	NM_016653.3(MAP3K20):c.987+9C>T	MAP3K20, MAP3K20-AS1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2041472	NM_016653.3(MAP3K20):c.1702+7_1702+10del	MAP3K20, MAP3K20-AS1	Deletion (intron variant)	not provided	GLikely benign

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