"Ambry Genetics"[submitter] AND "MAP3K15"[gene] - ClinVar

Search results

Items: 97

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2525337	NM_001001671.4(MAP3K15):c.3906G>C (p.Arg1302Ser)	MAP3K15, PDHA1 (R1302S)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3122906	NM_001001671.4(MAP3K15):c.3856C>T (p.Arg1286Trp)	MAP3K15, PDHA1 (R1286W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3293022	NM_001001671.4(MAP3K15):c.3839T>C (p.Leu1280Pro)	MAP3K15, PDHA1 (L1280P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3122905	NM_001001671.4(MAP3K15):c.3808G>T (p.Asp1270Tyr)	MAP3K15, PDHA1 (D1270Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3122904	NM_001001671.4(MAP3K15):c.3793G>A (p.Gly1265Ser)	MAP3K15, PDHA1 (G1265S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3122903	NM_001001671.4(MAP3K15):c.3773T>C (p.Ile1258Thr)	MAP3K15, PDHA1 (I1258T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3293029	NM_001001671.4(MAP3K15):c.3709G>A (p.Gly1237Arg)	MAP3K15, PDHA1 (G1237R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3293024	NM_001001671.4(MAP3K15):c.3709G>T (p.Gly1237Trp)	MAP3K15, PDHA1 (G1237W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2235893	NM_001001671.4(MAP3K15):c.3690G>C (p.Glu1230Asp)	MAP3K15, PDHA1 (E1230D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3122901	NM_001001671.4(MAP3K15):c.3668T>C (p.Leu1223Ser)	MAP3K15 (L1223S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494269	NM_001001671.4(MAP3K15):c.3496G>A (p.Gly1166Ser)	MAP3K15 (G1166S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209573	NM_001001671.4(MAP3K15):c.3379G>A (p.Ala1127Thr)	MAP3K15 (A1127T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597193	NM_001001671.4(MAP3K15):c.3353A>T (p.Asn1118Ile)	MAP3K15 (N1118I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213924	NM_001001671.4(MAP3K15):c.3217A>G (p.Lys1073Glu)	MAP3K15 (K1073E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209005	NM_001001671.4(MAP3K15):c.3178C>T (p.Arg1060Cys)	MAP3K15 (R1060C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122900	NM_001001671.4(MAP3K15):c.3155T>C (p.Ile1052Thr)	MAP3K15 (I1052T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608204	NM_001001671.4(MAP3K15):c.3118G>C (p.Glu1040Gln)	MAP3K15 (E1040Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268857	NM_001001671.4(MAP3K15):c.3049A>G (p.Lys1017Glu)	MAP3K15 (K1017E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122898	NM_001001671.4(MAP3K15):c.3035G>A (p.Arg1012His)	MAP3K15 (R1012H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364035	NM_001001671.4(MAP3K15):c.2947A>G (p.Ser983Gly)	MAP3K15 (S983G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3293019	NM_001001671.4(MAP3K15):c.2905C>T (p.Pro969Ser)	MAP3K15 (P969S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383796	NM_001001671.4(MAP3K15):c.2899C>T (p.Arg967Trp)	MAP3K15 (R967W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3293018	NM_001001671.4(MAP3K15):c.2881G>A (p.Ala961Thr)	MAP3K15 (A961T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285737	NM_001001671.4(MAP3K15):c.2830A>G (p.Ser944Gly)	MAP3K15 (S944G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325978	NM_001001671.4(MAP3K15):c.2791G>A (p.Val931Ile)	MAP3K15 (V931I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313647	NM_001001671.4(MAP3K15):c.2753G>A (p.Arg918Gln)	MAP3K15 (R918Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122897	NM_001001671.4(MAP3K15):c.2729A>G (p.Gln910Arg)	MAP3K15 (Q910R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122896	NM_001001671.4(MAP3K15):c.2668G>A (p.Glu890Lys)	MAP3K15 (E890K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272426	NM_001001671.4(MAP3K15):c.2667C>G (p.Phe889Leu)	MAP3K15 (F889L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255530	NM_001001671.4(MAP3K15):c.2549C>T (p.Pro850Leu)	MAP3K15 (P850L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286998	NM_001001671.4(MAP3K15):c.2491C>A (p.Pro831Thr)	MAP3K15 (P831T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600326	NM_001001671.4(MAP3K15):c.2387C>T (p.Ser796Leu)	MAP3K15 (S796L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122895	NM_001001671.4(MAP3K15):c.2308G>A (p.Val770Met)	MAP3K15 (V770M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262714	NM_001001671.4(MAP3K15):c.2293C>T (p.His765Tyr)	MAP3K15 (H765Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279047	NM_001001671.4(MAP3K15):c.2261C>G (p.Thr754Ser)	MAP3K15 (T754S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314973	NM_001001671.4(MAP3K15):c.2243C>T (p.Pro748Leu)	MAP3K15 (P748L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122894	NM_001001671.4(MAP3K15):c.2200C>T (p.Leu734Phe)	MAP3K15 (L734F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122893	NM_001001671.4(MAP3K15):c.2191G>A (p.Gly731Arg)	MAP3K15 (G731R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260950	NM_001001671.4(MAP3K15):c.2158G>A (p.Gly720Ser)	MAP3K15 (G720S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3293021	NM_001001671.4(MAP3K15):c.1954A>C (p.Asn652His)	MAP3K15 (N652H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252487	NM_001001671.4(MAP3K15):c.1919G>C (p.Gly640Ala)	MAP3K15 (G640A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621589	NM_001001671.4(MAP3K15):c.1892C>T (p.Thr631Met)	MAP3K15 (T631M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352478	NM_001001671.4(MAP3K15):c.1888A>T (p.Ser630Cys)	MAP3K15 (S630C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393203	NM_001001671.4(MAP3K15):c.1882G>A (p.Ala628Thr)	MAP3K15 (A628T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122891	NM_001001671.4(MAP3K15):c.1790A>G (p.His597Arg)	MAP3K15 (H597R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319417	NM_001001671.4(MAP3K15):c.1761T>G (p.Phe587Leu)	MAP3K15 (F587L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122889	NM_001001671.4(MAP3K15):c.1742G>A (p.Gly581Glu)	MAP3K15 (G581E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122888	NM_001001671.4(MAP3K15):c.1711G>A (p.Glu571Lys)	MAP3K15 (E571K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386132	NM_001001671.4(MAP3K15):c.1661G>A (p.Arg554Lys)	MAP3K15 (R554K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386175	NM_001001671.4(MAP3K15):c.1654G>A (p.Glu552Lys)	MAP3K15 (E552K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319883	NM_001001671.4(MAP3K15):c.1651G>T (p.Ala551Ser)	MAP3K15 (A551S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3293023	NM_001001671.4(MAP3K15):c.1623G>T (p.Gln541His)	MAP3K15 (Q541H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273576	NM_001001671.4(MAP3K15):c.1562A>G (p.Asn521Ser)	MAP3K15 (N521S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392781	NM_001001671.4(MAP3K15):c.1543A>G (p.Ile515Val)	MAP3K15 (I515V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122887	NM_001001671.4(MAP3K15):c.1517A>G (p.Gln506Arg)	MAP3K15 (Q506R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357011	NM_001001671.4(MAP3K15):c.1508C>T (p.Ser503Leu)	MAP3K15 (S503L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356748	NM_001001671.4(MAP3K15):c.1503A>C (p.Glu501Asp)	MAP3K15 (E501D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486615	NM_001001671.4(MAP3K15):c.1502A>G (p.Glu501Gly)	MAP3K15 (E501G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547252	NM_001001671.4(MAP3K15):c.1477C>T (p.Arg493Trp)	MAP3K15 (R493W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122885	NM_001001671.4(MAP3K15):c.1448G>A (p.Arg483Gln)	MAP3K15 (R483Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614928	NM_001001671.4(MAP3K15):c.1403C>T (p.Ala468Val)	MAP3K15 (A468V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532288	NM_001001671.4(MAP3K15):c.1328T>G (p.Met443Arg)	MAP3K15 (M443R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340142	NM_001001671.4(MAP3K15):c.1299G>C (p.Leu433Phe)	MAP3K15 (L433F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122884	NM_001001671.4(MAP3K15):c.1295G>C (p.Ser432Thr)	MAP3K15 (S432T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122883	NM_001001671.4(MAP3K15):c.1286G>A (p.Arg429Gln)	MAP3K15 (R429Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393296	NM_001001671.4(MAP3K15):c.1285C>G (p.Arg429Gly)	MAP3K15 (R429G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313281	NM_001001671.4(MAP3K15):c.1285C>T (p.Arg429Trp)	MAP3K15 (R429W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3293025	NM_001001671.4(MAP3K15):c.1210A>G (p.Ile404Val)	MAP3K15 (I404V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122880	NM_001001671.4(MAP3K15):c.1147C>T (p.Arg383Cys)	MAP3K15 (R383C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377446	NM_001001671.4(MAP3K15):c.1139A>G (p.Asp380Gly)	MAP3K15 (D380G)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2252356	NM_001001671.4(MAP3K15):c.1133A>G (p.Lys378Arg)	MAP3K15 (K378R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3293030	NM_001001671.4(MAP3K15):c.1132A>G (p.Lys378Glu)	MAP3K15 (K378E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122879	NM_001001671.4(MAP3K15):c.1051C>G (p.Gln351Glu)	MAP3K15 (Q351E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122878	NM_001001671.4(MAP3K15):c.1036A>G (p.Met346Val)	MAP3K15 (M346V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2298637	NM_001001671.4(MAP3K15):c.970T>C (p.Phe324Leu)	MAP3K15 (F324L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2412539	NM_001001671.4(MAP3K15):c.964A>G (p.Ile322Val)	MAP3K15 (I322V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547253	NM_001001671.4(MAP3K15):c.930G>A (p.Met310Ile)	MAP3K15 (M310I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490391	NM_001001671.4(MAP3K15):c.901A>T (p.Met301Leu)	MAP3K15 (M301L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3293027	NM_001001671.4(MAP3K15):c.899C>T (p.Ala300Val)	MAP3K15 (A300V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252140	NM_001001671.4(MAP3K15):c.865C>T (p.Leu289Phe)	MAP3K15 (L289F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3293026	NM_001001671.4(MAP3K15):c.818G>A (p.Arg273His)	MAP3K15 (R273H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122908	NM_001001671.4(MAP3K15):c.806G>A (p.Arg269Gln)	MAP3K15 (R269Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212394	NM_001001671.4(MAP3K15):c.698A>C (p.Lys233Thr)	MAP3K15 (K233T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3293028	NM_001001671.4(MAP3K15):c.625A>C (p.Met209Leu)	MAP3K15 (M209L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2237635	NM_001001671.4(MAP3K15):c.462G>T (p.Leu154Phe)	MAP3K15 (L154F)	Single nucleotide variant (missense variant)	MAP3K15-related disorder +1 more	GUncertain significance
Select item 3122907	NM_001001671.4(MAP3K15):c.448A>G (p.Asn150Asp)	MAP3K15 (N150D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364086	NM_001001671.4(MAP3K15):c.442A>G (p.Met148Val)	MAP3K15 (M148V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401119	NM_001001671.4(MAP3K15):c.419T>C (p.Leu140Pro)	MAP3K15 (L140P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408703	NM_001001671.4(MAP3K15):c.416A>G (p.His139Arg)	MAP3K15 (H139R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2236543	NM_001001671.4(MAP3K15):c.251G>C (p.Arg84Pro)	MAP3K15 (R84P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611326	NM_001001671.4(MAP3K15):c.217G>T (p.Gly73Cys)	MAP3K15 (G73C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2282209	NM_001001671.4(MAP3K15):c.206A>C (p.Glu69Ala)	MAP3K15 (E69A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2568725	NM_001001671.4(MAP3K15):c.205G>A (p.Glu69Lys)	MAP3K15 (E69K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296883	NM_001001671.4(MAP3K15):c.199C>A (p.Arg67Ser)	MAP3K15 (R67S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481583	NM_001001671.4(MAP3K15):c.188C>A (p.Ala63Glu)	MAP3K15 (A63E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3293020	NM_001001671.4(MAP3K15):c.169C>T (p.Pro57Ser)	MAP3K15 (P57S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2232599	NM_001001671.4(MAP3K15):c.128G>A (p.Gly43Asp)	MAP3K15 (G43D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 97