"Ambry Genetics"[submitter] AND "PLXND1"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2279806	NM_015103.3(PLXND1):c.5767A>G (p.Ser1923Gly)	PLXND1 (S1923G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205479	NM_015103.3(PLXND1):c.5641G>A (p.Ala1881Thr)	PLXND1 (A1881T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411009	NM_015103.3(PLXND1):c.5550G>T (p.Glu1850Asp)	PLXND1 (E1850D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527111	NM_015103.3(PLXND1):c.5548G>A (p.Glu1850Lys)	PLXND1 (E1850K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607249	NM_015103.3(PLXND1):c.5497A>G (p.Lys1833Glu)	PLXND1 (K1833E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308009	NM_015103.3(PLXND1):c.5351A>G (p.Asp1784Gly)	LOC112872301, PLXND1 (D1784G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2277921	NM_015103.3(PLXND1):c.5323A>G (p.Ile1775Val)	LOC112872301, PLXND1 (I1775V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399087	NM_015103.3(PLXND1):c.5044G>C (p.Glu1682Gln)	PLXND1 (E1682Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308007	NM_015103.3(PLXND1):c.5038A>G (p.Thr1680Ala)	PLXND1 (T1680A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308005	NM_015103.3(PLXND1):c.4991G>A (p.Arg1664Gln)	PLXND1 (R1664Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482017	NM_015103.3(PLXND1):c.4969A>G (p.Lys1657Glu)	PLXND1 (K1657E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215763	NM_015103.3(PLXND1):c.4898G>A (p.Arg1633His)	PLXND1 (R1633H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215762	NM_015103.3(PLXND1):c.4885G>A (p.Val1629Met)	PLXND1 (V1629M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308008	NM_015103.3(PLXND1):c.4862G>A (p.Arg1621Gln)	PLXND1 (R1621Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324893	NM_015103.3(PLXND1):c.4821C>A (p.Asp1607Glu)	PLXND1 (D1607E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2266697	NM_015103.3(PLXND1):c.4805G>T (p.Arg1602Leu)	PLXND1 (R1602L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215761	NM_015103.3(PLXND1):c.4779G>C (p.Lys1593Asn)	PLXND1 (K1593N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215760	NM_015103.3(PLXND1):c.4715T>C (p.Val1572Ala)	PLXND1 (V1572A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558320	NM_015103.3(PLXND1):c.4699A>G (p.Met1567Val)	PLXND1 (M1567V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215759	NM_015103.3(PLXND1):c.4667G>A (p.Arg1556Gln)	PLXND1 (R1556Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296226	NM_015103.3(PLXND1):c.4666C>T (p.Arg1556Trp)	PLXND1 (R1556W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217753	NM_015103.3(PLXND1):c.4575C>G (p.Ile1525Met)	PLXND1 (I1525M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251550	NM_015103.3(PLXND1):c.4536G>C (p.Glu1512Asp)	PLXND1 (E1512D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337212	NM_015103.3(PLXND1):c.4462T>C (p.Ser1488Pro)	PLXND1 (S1488P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540146	NM_015103.3(PLXND1):c.4360G>A (p.Gly1454Ser)	PLXND1 (G1454S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215758	NM_015103.3(PLXND1):c.4315C>T (p.Arg1439Cys)	PLXND1 (R1439C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411504	NM_015103.3(PLXND1):c.4310C>T (p.Ala1437Val)	PLXND1 (A1437V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241712	NM_015103.3(PLXND1):c.4244C>T (p.Ser1415Leu)	PLXND1 (S1415L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215756	NM_015103.3(PLXND1):c.4216A>G (p.Met1406Val)	PLXND1 (M1406V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555459	NM_015103.3(PLXND1):c.4207C>T (p.Arg1403Trp)	PLXND1 (R1403W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556402	NM_015103.3(PLXND1):c.4114G>T (p.Val1372Leu)	PLXND1 (V1372L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308003	NM_015103.3(PLXND1):c.4109G>A (p.Arg1370His)	PLXND1 (R1370H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215755	NM_015103.3(PLXND1):c.4056G>C (p.Lys1352Asn)	PLXND1 (K1352N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302464	NM_015103.3(PLXND1):c.3873C>G (p.Phe1291Leu)	PLXND1 (F1291L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222158	NM_015103.3(PLXND1):c.3862G>A (p.Val1288Met)	PLXND1 (V1288M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2232622	NM_015103.3(PLXND1):c.3725C>T (p.Ala1242Val)	PLXND1 (A1242V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2269317	NM_015103.3(PLXND1):c.3724G>T (p.Ala1242Ser)	PLXND1 (A1242S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215754	NM_015103.3(PLXND1):c.3714G>C (p.Glu1238Asp)	PLXND1 (E1238D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215753	NM_015103.3(PLXND1):c.3587C>G (p.Thr1196Ser)	PLXND1 (T1196S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215752	NM_015103.3(PLXND1):c.3493G>A (p.Gly1165Ser)	PLXND1 (G1165S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366459	NM_015103.3(PLXND1):c.3491G>A (p.Arg1164Gln)	PLXND1 (R1164Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215751	NM_015103.3(PLXND1):c.3490C>T (p.Arg1164Trp)	PLXND1 (R1164W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598937	NM_015103.3(PLXND1):c.3478G>A (p.Glu1160Lys)	PLXND1 (E1160K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308010	NM_015103.3(PLXND1):c.3469C>G (p.Leu1157Val)	PLXND1 (L1157V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457063	NM_015103.3(PLXND1):c.3404C>T (p.Ala1135Val)	PLXND1 (A1135V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215750	NM_015103.3(PLXND1):c.3326G>A (p.Arg1109Gln)	PLXND1 (R1109Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2531817	NM_015103.3(PLXND1):c.3325C>T (p.Arg1109Trp)	PLXND1 (R1109W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216313	NM_015103.3(PLXND1):c.3323G>A (p.Gly1108Asp)	PLXND1 (G1108D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318644	NM_015103.3(PLXND1):c.3310G>A (p.Val1104Ile)	PLXND1 (V1104I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394318	NM_015103.3(PLXND1):c.3295A>C (p.Asn1099His)	PLXND1 (N1099H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221514	NM_015103.3(PLXND1):c.3233G>A (p.Arg1078His)	PLXND1 (R1078H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397924	NM_015103.3(PLXND1):c.3215C>T (p.Thr1072Met)	PLXND1 (T1072M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383934	NM_015103.3(PLXND1):c.3179A>G (p.Asn1060Ser)	PLXND1 (N1060S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305644	NM_015103.3(PLXND1):c.3175G>C (p.Gly1059Arg)	PLXND1 (G1059R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308014	NM_015103.3(PLXND1):c.3169G>T (p.Val1057Leu)	PLXND1 (V1057L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218170	NM_015103.3(PLXND1):c.3164G>C (p.Gly1055Ala)	PLXND1 (G1055A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215749	NM_015103.3(PLXND1):c.3154G>C (p.Glu1052Gln)	PLXND1 (E1052Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308013	NM_015103.3(PLXND1):c.3136C>T (p.Pro1046Ser)	PLXND1 (P1046S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476059	NM_015103.3(PLXND1):c.3079C>G (p.Arg1027Gly)	PLXND1 (R1027G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250328	NM_015103.3(PLXND1):c.3079C>T (p.Arg1027Cys)	PLXND1 (R1027C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215748	NM_015103.3(PLXND1):c.3068C>T (p.Thr1023Met)	PLXND1 (T1023M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215746	NM_015103.3(PLXND1):c.3047T>C (p.Val1016Ala)	PLXND1 (V1016A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258665	NM_015103.3(PLXND1):c.3026G>T (p.Gly1009Val)	PLXND1 (G1009V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596434	NM_015103.3(PLXND1):c.3018C>T (p.Leu1006=)	PLXND1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3215745	NM_015103.3(PLXND1):c.2954C>T (p.Ser985Phe)	PLXND1 (S985F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508154	NM_015103.3(PLXND1):c.2924G>A (p.Arg975His)	PLXND1 (R975H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215744	NM_015103.3(PLXND1):c.2864C>T (p.Pro955Leu)	PLXND1 (P955L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310352	NM_015103.3(PLXND1):c.2860G>A (p.Ala954Thr)	PLXND1 (A954T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408010	NM_015103.3(PLXND1):c.2792G>T (p.Gly931Val)	PLXND1 (G931V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308001	NM_015103.3(PLXND1):c.2735G>A (p.Arg912Gln)	PLXND1 (R912Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258975	NM_015103.3(PLXND1):c.2705C>A (p.Pro902Gln)	PLXND1 (P902Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332723	NM_015103.3(PLXND1):c.2635G>A (p.Gly879Arg)	PLXND1 (G879R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595834	NM_015103.3(PLXND1):c.2627G>A (p.Arg876His)	PLXND1 (R876H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215742	NM_015103.3(PLXND1):c.2515C>T (p.Pro839Ser)	PLXND1 (P839S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215808	NM_015103.3(PLXND1):c.2501G>A (p.Arg834Gln)	PLXND1 (R834Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215741	NM_015103.3(PLXND1):c.2485A>G (p.Lys829Glu)	PLXND1 (K829E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620604	NM_015103.3(PLXND1):c.2480A>C (p.Gln827Pro)	PLXND1 (Q827P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588954	NM_015103.3(PLXND1):c.2458C>G (p.Gln820Glu)	PLXND1 (Q820E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2336543	NM_015103.3(PLXND1):c.2426A>T (p.Asp809Val)	PLXND1 (D809V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308002	NM_015103.3(PLXND1):c.2389G>A (p.Glu797Lys)	PLXND1 (E797K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215740	NM_015103.3(PLXND1):c.2343C>G (p.Phe781Leu)	PLXND1 (F781L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545828	NM_015103.3(PLXND1):c.2261G>A (p.Arg754Gln)	PLXND1 (R754Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2689791	NM_015103.3(PLXND1):c.2240C>T (p.Thr747Met)	PLXND1 (T747M)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3215738	NM_015103.3(PLXND1):c.2224G>T (p.Ala742Ser)	PLXND1 (A742S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366338	NM_015103.3(PLXND1):c.2110C>T (p.Arg704Cys)	PLXND1 (R704C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308012	NM_015103.3(PLXND1):c.2086A>G (p.Asn696Asp)	PLXND1 (N696D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353327	NM_015103.3(PLXND1):c.2024A>G (p.Asn675Ser)	PLXND1 (N675S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215737	NM_015103.3(PLXND1):c.2021C>G (p.Pro674Arg)	PLXND1 (P674R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293353	NM_015103.3(PLXND1):c.1994C>T (p.Pro665Leu)	PLXND1 (P665L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215736	NM_015103.3(PLXND1):c.1942C>T (p.Arg648Trp)	PLXND1 (R648W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364304	NM_015103.3(PLXND1):c.1831G>A (p.Asp611Asn)	PLXND1 (D611N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551501	NM_015103.3(PLXND1):c.1829T>C (p.Ile610Thr)	PLXND1 (I610T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465640	NM_015103.3(PLXND1):c.1720C>T (p.Arg574Trp)	PLXND1 (R574W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215734	NM_015103.3(PLXND1):c.1718C>T (p.Thr573Met)	PLXND1 (T573M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615608	NM_015103.3(PLXND1):c.1678G>C (p.Gly560Arg)	PLXND1 (G560R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519777	NM_015103.3(PLXND1):c.1643C>T (p.Ala548Val)	PLXND1 (A548V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217428	NM_015103.3(PLXND1):c.1610C>T (p.Thr537Met)	PLXND1 (T537M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2203924	NM_015103.3(PLXND1):c.1569G>A (p.Met523Ile)	PLXND1 (M523I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361754	NM_015103.3(PLXND1):c.1502A>G (p.Glu501Gly)	PLXND1 (E501G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215733	NM_015103.3(PLXND1):c.1459C>G (p.Leu487Val)	PLXND1 (L487V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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