ClinVar for Gene (Select 23129) - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 1 to 100 of 289

<< First< Prev

Page of 3

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3336931	NM_015103.3(PLXND1):c.3676del (p.Ile1226fs)	PLXND1 (I1226fs)	Deletion (frameshift variant)	not provided	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 3308013	NM_015103.3(PLXND1):c.3136C>T (p.Pro1046Ser)	PLXND1 (P1046S)	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 3308010	NM_015103.3(PLXND1):c.3469C>G (p.Leu1157Val)	PLXND1 (L1157V)	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 3308008	NM_015103.3(PLXND1):c.4862G>A (p.Arg1621Gln)	PLXND1 (R1621Q)	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 3308006	NM_015103.3(PLXND1):c.266T>C (p.Leu89Pro)	PLXND1 (L89P)	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 3308004	NM_015103.3(PLXND1):c.128G>C (p.Arg43Pro)	PLXND1 (R43P)	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 3308002	NM_015103.3(PLXND1):c.2389G>A (p.Glu797Lys)	PLXND1 (E797K)	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 3251026	NM_015103.3(PLXND1):c.4065G>A (p.Val1355=)	PLXND1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3215768	NM_015103.3(PLXND1):c.974A>T (p.His325Leu)	PLXND1 (H325L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215767	NM_015103.3(PLXND1):c.76C>G (p.Pro26Ala)	PLXND1 (P26A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215766	NM_015103.3(PLXND1):c.688C>T (p.His230Tyr)	PLXND1 (H230Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215765	NM_015103.3(PLXND1):c.611G>C (p.Gly204Ala)	PLXND1 (G204A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215764	NM_015103.3(PLXND1):c.583G>A (p.Val195Ile)	PLXND1 (V195I)	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 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 3215759	NM_015103.3(PLXND1):c.4667G>A (p.Arg1556Gln)	PLXND1 (R1556Q)	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 3215756	NM_015103.3(PLXND1):c.4216A>G (p.Met1406Val)	PLXND1 (M1406V)	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 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 3215751	NM_015103.3(PLXND1):c.3490C>T (p.Arg1164Trp)	PLXND1 (R1164W)	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 3215749	NM_015103.3(PLXND1):c.3154G>C (p.Glu1052Gln)	PLXND1 (E1052Q)	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 3215745	NM_015103.3(PLXND1):c.2954C>T (p.Ser985Phe)	PLXND1 (S985F)	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 3215742	NM_015103.3(PLXND1):c.2515C>T (p.Pro839Ser)	PLXND1 (P839S)	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 3215740	NM_015103.3(PLXND1):c.2343C>G (p.Phe781Leu)	PLXND1 (F781L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215739	NM_015103.3(PLXND1):c.22G>A (p.Gly8Ser)	PLXND1 (G8S)	Single nucleotide variant (missense variant)	not specified	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 3215737	NM_015103.3(PLXND1):c.2021C>G (p.Pro674Arg)	PLXND1 (P674R)	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 3215734	NM_015103.3(PLXND1):c.1718C>T (p.Thr573Met)	PLXND1 (T573M)	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
Select item 3215732	NM_015103.3(PLXND1):c.1426G>A (p.Val476Met)	PLXND1 (V476M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215731	NM_015103.3(PLXND1):c.1393G>A (p.Val465Met)	PLXND1 (V465M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215730	NM_015103.3(PLXND1):c.10C>T (p.Arg4Cys)	PLXND1 (R4C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215729	NM_015103.3(PLXND1):c.1070G>A (p.Arg357His)	PLXND1 (R357H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3060694	NM_015103.3(PLXND1):c.3879C>T (p.Phe1293=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related disorder	GBenign
Select item 3060610	NM_015103.3(PLXND1):c.4994-4A>G	PLXND1	Single nucleotide variant (intron variant)	PLXND1-related disorder	GBenign
Select item 3060582	NM_015103.3(PLXND1):c.2295G>C (p.Thr765=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related disorder	GBenign
Select item 3060415	NM_015103.3(PLXND1):c.2608A>G (p.Met870Val)	PLXND1 (M870V)	Single nucleotide variant (missense variant)	PLXND1-related disorder	GBenign
Select item 3060110	NM_015103.3(PLXND1):c.3973+10G>T	PLXND1	Single nucleotide variant (intron variant)	PLXND1-related disorder	GBenign
Select item 3059893	NM_015103.3(PLXND1):c.1473C>T (p.Asn491=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related disorder	GBenign
Select item 3059889	NM_015103.3(PLXND1):c.5727G>A (p.Gln1909=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related disorder	GBenign
Select item 3059215	NM_015103.3(PLXND1):c.4008C>G (p.Leu1336=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related disorder	GBenign
Select item 3059112	NM_015103.3(PLXND1):c.3396C>T (p.Asn1132=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related disorder	GBenign
Select item 3056786	NM_015103.3(PLXND1):c.1849C>T (p.Pro617Ser)	PLXND1 (P617S)	Single nucleotide variant (missense variant)	PLXND1-related disorder	GBenign
Select item 3056681	NM_015103.3(PLXND1):c.2034C>T (p.His678=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related disorder	GBenign
Select item 3056466	NM_015103.3(PLXND1):c.3627G>A (p.Gln1209=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related disorder	GBenign
Select item 3056384	NM_015103.3(PLXND1):c.966C>T (p.Cys322=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related disorder	GLikely benign
Select item 3055934	NM_015103.3(PLXND1):c.3030C>T (p.Ser1010=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related disorder	GBenign
Select item 3055714	NM_015103.3(PLXND1):c.1591G>A (p.Gly531Ser)	PLXND1 (G531S)	Single nucleotide variant (missense variant)	PLXND1-related disorder	GBenign
Select item 3055313	NM_015103.3(PLXND1):c.2196C>T (p.Ser732=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related disorder	GBenign
Select item 3050361	NM_015103.3(PLXND1):c.3453T>C (p.Ala1151=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related disorder	GLikely benign
Select item 3050325	NM_015103.3(PLXND1):c.5646G>A (p.Lys1882=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related disorder	GLikely benign
Select item 3049180	NM_015103.3(PLXND1):c.4954A>G (p.Met1652Val)	PLXND1 (M1652V)	Single nucleotide variant (missense variant)	PLXND1-related disorder	GLikely benign
Select item 3044790	NM_015103.3(PLXND1):c.4311G>A (p.Ala1437=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related disorder	GLikely benign
Select item 3042381	NM_015103.3(PLXND1):c.609G>A (p.Gly203=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related disorder	GLikely benign
Select item 3040194	NM_015103.3(PLXND1):c.474C>T (p.Ala158=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related disorder	GLikely benign
Select item 3034585	NM_015103.3(PLXND1):c.1845G>A (p.Glu615=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related disorder	GLikely benign
Select item 3033777	NM_015103.3(PLXND1):c.5640C>T (p.Tyr1880=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related disorder	GLikely benign
Select item 2920786	NM_015103.3(PLXND1):c.2870C>T (p.Pro957Leu)	PLXND1 (P957L)	Single nucleotide variant (missense variant)	Congenital heart defects, multiple types, 9	GUncertain significance
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 2672958	NM_015103.3(PLXND1):c.4466T>C (p.Val1489Ala)	PLXND1 (V1489A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2654129	NM_015103.3(PLXND1):c.1466C>T (p.Thr489Met)	PLXND1 (T489M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2654128	NM_015103.3(PLXND1):c.1578C>G (p.Asp526Glu)	PLXND1 (D526E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2654127	NM_015103.3(PLXND1):c.4086+8C>T	PLXND1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2636221	NM_015103.3(PLXND1):c.4682C>T (p.Ser1561Phe)	PLXND1 (S1561F)	Single nucleotide variant (missense variant)	PLXND1-related disorder	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 2617831	NM_015103.3(PLXND1):c.125C>T (p.Ala42Val)	PLXND1 (A42V)	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 2614220	NM_015103.3(PLXND1):c.1087C>T (p.Pro363Ser)	PLXND1 (P363S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613333	NM_015103.3(PLXND1):c.991G>T (p.Ala331Ser)	PLXND1 (A331S)	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 2603061	NM_015103.3(PLXND1):c.1420G>A (p.Val474Met)	PLXND1 (V474M)	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 2596434	NM_015103.3(PLXND1):c.3018C>T (p.Leu1006=)	PLXND1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
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 2588954	NM_015103.3(PLXND1):c.2458C>G (p.Gln820Glu)	PLXND1 (Q820E)	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 2556402	NM_015103.3(PLXND1):c.4114G>T (p.Val1372Leu)	PLXND1 (V1372L)	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 2551501	NM_015103.3(PLXND1):c.1829T>C (p.Ile610Thr)	PLXND1 (I610T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547966	NM_015103.3(PLXND1):c.128G>A (p.Arg43Gln)	PLXND1 (R43Q)	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 2540146	NM_015103.3(PLXND1):c.4360G>A (p.Gly1454Ser)	PLXND1 (G1454S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

<< First< Prev

Page of 3