"Ambry Genetics"[submitter] AND "MAP4"[gene] - ClinVar

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Items: 62

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2544122	NM_001385682.1(MAP4):c.6800C>T (p.Ala2267Val)	MAP4 (A1000V +74 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2470328	NM_001385682.1(MAP4):c.6755C>T (p.Pro2252Leu)	MAP4 (P1000L +74 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3123062	NM_001385682.1(MAP4):c.6736C>G (p.Pro2246Ala)	MAP4 (P1009A +74 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2516658	NM_001385682.1(MAP4):c.6721C>T (p.Pro2241Ser)	MAP4 (P1004S +74 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3123061	NM_001385682.1(MAP4):c.6715G>A (p.Glu2239Lys)	MAP4 (E987K +74 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2475761	NM_001385682.1(MAP4):c.6706G>C (p.Gly2236Arg)	MAP4 (G1007R +74 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2309206	NM_001385682.1(MAP4):c.6658G>A (p.Asp2220Asn)	MAP4 (D1003N +72 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2209088	NM_001385682.1(MAP4):c.6496G>C (p.Gly2166Arg)	MAP4 (G1018R +49 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2313283	NM_001385682.1(MAP4):c.6401C>A (p.Ala2134Glu)	MAP4 (A461E +39 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2459998	NM_001385682.1(MAP4):c.6374C>T (p.Pro2125Leu)	MAP4 (P1009L +39 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2613196	NM_001385682.1(MAP4):c.6335G>A (p.Arg2112Gln)	MAP4 (R518Q +39 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2541629	NM_001385682.1(MAP4):c.6328A>G (p.Thr2110Ala)	MAP4 (T2110A +39 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2604021	NM_001385682.1(MAP4):c.6311A>C (p.Lys2104Thr)	MAP4 (K510T +39 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2229615	NM_001385682.1(MAP4):c.6237T>A (p.Asn2079Lys)	MAP4 (N2039K +41 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274127	NM_001385682.1(MAP4):c.6220G>A (p.Ala2074Thr)	MAP4 (A2050T +41 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318484	NM_001385682.1(MAP4):c.6125G>C (p.Arg2042Pro)	MAP4 (R2042P +41 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516057	NM_001385682.1(MAP4):c.6085G>A (p.Val2029Met)	MAP4 (V1989M +41 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3123059	NM_001385682.1(MAP4):c.6065G>A (p.Gly2022Glu)	MAP4 (G1998E +41 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2327093	NM_001385682.1(MAP4):c.6004G>A (p.Asp2002Asn)	MAP4 (D2002N +41 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275211	NM_001385682.1(MAP4):c.5885C>A (p.Ala1962Asp)	MAP4 (A1938D +41 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219376	NM_001385682.1(MAP4):c.5884G>C (p.Ala1962Pro)	MAP4 (A327P +41 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302662	NM_001385682.1(MAP4):c.5876C>G (p.Ala1959Gly)	MAP4 (A1919G +41 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515420	NM_001385682.1(MAP4):c.5851A>C (p.Thr1951Pro)	MAP4 (T326P +41 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265131	NM_001385682.1(MAP4):c.5789G>A (p.Arg1930Gln)	MAP4 (R1906Q +41 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3123057	NM_001385682.1(MAP4):c.5762T>C (p.Ile1921Thr)	MAP4 (I263T +41 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302151	NM_001385682.1(MAP4):c.5681C>A (p.Pro1894Gln)	MAP4 (P642Q +31 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3123056	NM_001385682.1(MAP4):c.5672G>C (p.Gly1891Ala)	MAP4 (G256A +31 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2402731	NM_001385682.1(MAP4):c.5588A>C (p.Lys1863Thr)	MAP4 (K205T +24 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2271588	NM_001385682.1(MAP4):c.5474G>C (p.Gly1825Ala)	MAP4 (G167A +24 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3123055	NM_001385682.1(MAP4):c.5456G>A (p.Gly1819Glu)	MAP4 (G266E +24 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516578	NM_001385682.1(MAP4):c.5438T>A (p.Ile1813Lys)	MAP4 (I457K +24 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3123054	NM_001385682.1(MAP4):c.1956A>C (p.Lys652Asn)	MAP4 (K203N +20 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2545986	NM_001385682.1(MAP4):c.1922A>G (p.Glu641Gly)	MAP4 (E192G +19 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2256509	NM_001385682.1(MAP4):c.1892C>G (p.Thr631Arg)	MAP4 (T420R +19 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3123053	NM_001385682.1(MAP4):c.1883T>C (p.Val628Ala)	MAP4 (V417A +21 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2399193	NM_001385682.1(MAP4):c.1855C>T (p.Pro619Ser)	MAP4 (P578S +17 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2620839	NM_001385682.1(MAP4):c.1793A>C (p.Gln598Pro)	MAP4 (Q450P +17 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3123052	NM_001385682.1(MAP4):c.1649C>T (p.Pro550Leu)	MAP4 (P402L +17 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2341192	NM_001385682.1(MAP4):c.1591A>G (p.Ile531Val)	MAP4 (I429V +17 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2353105	NM_001385682.1(MAP4):c.1481C>T (p.Pro494Leu)	MAP4 (P392L +17 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2295400	NM_001385682.1(MAP4):c.1472A>T (p.Asp491Val)	MAP4 (D280V +17 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2368136	NM_001385682.1(MAP4):c.1463C>T (p.Pro488Leu)	MAP4 (P277L +17 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2271359	NM_001385682.1(MAP4):c.1361C>T (p.Pro454Leu)	MAP4 (P243L +17 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2288106	NM_001385682.1(MAP4):c.1184A>C (p.Asp395Ala)	MAP4 (D316A +16 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2363775	NM_001385682.1(MAP4):c.1093G>T (p.Ala365Ser)	MAP4 (A301S +16 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2284072	NM_001385682.1(MAP4):c.1078A>G (p.Ile360Val)	MAP4 (I330V +16 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2406510	NM_001385682.1(MAP4):c.980A>T (p.Asp327Val)	MAP4 (D179V +16 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2254825	NM_001385682.1(MAP4):c.931G>A (p.Glu311Lys)	MAP4 (E204K +16 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3123067	NM_001385682.1(MAP4):c.853G>A (p.Asp285Asn)	MAP4 (D137N +16 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2609404	NM_001385682.1(MAP4):c.852A>T (p.Leu284Phe)	MAP4 (L136F +16 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3123066	NM_001385682.1(MAP4):c.833T>C (p.Met278Thr)	MAP4 (M255T +16 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3123065	NM_001385682.1(MAP4):c.811G>A (p.Glu271Lys)	MAP4 (E123K +16 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2494033	NM_001385682.1(MAP4):c.742A>G (p.Thr248Ala)	MAP4 (T184A +16 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3123064	NM_001385682.1(MAP4):c.634C>A (p.Pro212Thr)	MAP4 (P105T +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3123063	NM_001385682.1(MAP4):c.593C>T (p.Pro198Leu)	MAP4 (P119L +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2259398	NM_001385682.1(MAP4):c.427A>T (p.Met143Leu)	MAP4 (M155L +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2593529	NM_001385682.1(MAP4):c.368C>T (p.Thr123Ile)	MAP4 (T123I +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2475461	NM_001385682.1(MAP4):c.308T>C (p.Phe103Ser)	MAP4 (F115S +5 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2494940	NM_001385682.1(MAP4):c.302C>T (p.Thr101Ile)	MAP4 (T113I +5 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2608985	NM_001385682.1(MAP4):c.301A>T (p.Thr101Ser)	MAP4 (T101S +5 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2341705	NM_001385682.1(MAP4):c.219T>G (p.Ile73Met)	MAP4 (I73M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2588695	NM_001385682.1(MAP4):c.134C>A (p.Thr45Lys)	MAP4 (T45K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 62