ClinVar for Gene (Select 23129) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3060694	NM_015103.3(PLXND1):c.3879C>T (p.Phe1293=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related condition	GBenign
Select item 3060610	NM_015103.3(PLXND1):c.4994-4A>G	PLXND1	Single nucleotide variant (intron variant)	PLXND1-related condition	GBenign
Select item 3060582	NM_015103.3(PLXND1):c.2295G>C (p.Thr765=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related condition	GBenign
Select item 3060415	NM_015103.3(PLXND1):c.2608A>G (p.Met870Val)	PLXND1 (M870V)	Single nucleotide variant (missense variant)	PLXND1-related condition	GBenign
Select item 3060110	NM_015103.3(PLXND1):c.3973+10G>T	PLXND1	Single nucleotide variant (intron variant)	PLXND1-related condition	GBenign
Select item 3059893	NM_015103.3(PLXND1):c.1473C>T (p.Asn491=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related condition	GBenign
Select item 3059889	NM_015103.3(PLXND1):c.5727G>A (p.Gln1909=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related condition	GBenign
Select item 3059215	NM_015103.3(PLXND1):c.4008C>G (p.Leu1336=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related condition	GBenign
Select item 3059112	NM_015103.3(PLXND1):c.3396C>T (p.Asn1132=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related condition	GBenign
Select item 3056786	NM_015103.3(PLXND1):c.1849C>T (p.Pro617Ser)	PLXND1 (P617S)	Single nucleotide variant (missense variant)	PLXND1-related condition	GBenign
Select item 3056681	NM_015103.3(PLXND1):c.2034C>T (p.His678=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related condition	GBenign
Select item 3056466	NM_015103.3(PLXND1):c.3627G>A (p.Gln1209=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related condition	GBenign
Select item 3056384	NM_015103.3(PLXND1):c.966C>T (p.Cys322=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related condition	GLikely benign
Select item 3055934	NM_015103.3(PLXND1):c.3030C>T (p.Ser1010=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related condition	GBenign
Select item 3055714	NM_015103.3(PLXND1):c.1591G>A (p.Gly531Ser)	PLXND1 (G531S)	Single nucleotide variant (missense variant)	PLXND1-related condition	GBenign
Select item 3055313	NM_015103.3(PLXND1):c.2196C>T (p.Ser732=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related condition	GBenign
Select item 3050361	NM_015103.3(PLXND1):c.3453T>C (p.Ala1151=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related condition	GLikely benign
Select item 3050325	NM_015103.3(PLXND1):c.5646G>A (p.Lys1882=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related condition	GLikely benign
Select item 3049180	NM_015103.3(PLXND1):c.4954A>G (p.Met1652Val)	PLXND1 (M1652V)	Single nucleotide variant (missense variant)	PLXND1-related condition	GLikely benign
Select item 3044790	NM_015103.3(PLXND1):c.4311G>A (p.Ala1437=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related condition	GLikely benign
Select item 3042381	NM_015103.3(PLXND1):c.609G>A (p.Gly203=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related condition	GLikely benign
Select item 3040194	NM_015103.3(PLXND1):c.474C>T (p.Ala158=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related condition	GLikely benign
Select item 3034585	NM_015103.3(PLXND1):c.1845G>A (p.Glu615=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related condition	GLikely benign
Select item 3033777	NM_015103.3(PLXND1):c.5640C>T (p.Tyr1880=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related condition	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)	Congenital heart defects, multiple types, 9	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)	PLXND1-related condition +1 more	GConflicting classifications of pathogenicity
Select item 2654127	NM_015103.3(PLXND1):c.4086+8C>T	PLXND1	Single nucleotide variant (intron variant)	PLXND1-related condition +1 more	GBenign
Select item 2636221	NM_015103.3(PLXND1):c.4682C>T (p.Ser1561Phe)	PLXND1 (S1561F)	Single nucleotide variant (missense variant)	PLXND1-related condition	GUncertain significance
Select item 2620604	NM_015103.3(PLXND1):c.2480A>C (p.Gln827Pro)	PLXND1 (Q827P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2617831	NM_015103.3(PLXND1):c.125C>T (p.Ala42Val)	PLXND1 (A42V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2615608	NM_015103.3(PLXND1):c.1678G>C (p.Gly560Arg)	PLXND1 (G560R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2614220	NM_015103.3(PLXND1):c.1087C>T (p.Pro363Ser)	PLXND1 (P363S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2613333	NM_015103.3(PLXND1):c.991G>T (p.Ala331Ser)	PLXND1 (A331S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2607249	NM_015103.3(PLXND1):c.5497A>G (p.Lys1833Glu)	PLXND1 (K1833E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2603061	NM_015103.3(PLXND1):c.1420G>A (p.Val474Met)	PLXND1 (V474M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2598937	NM_015103.3(PLXND1):c.3478G>A (p.Glu1160Lys)	PLXND1 (E1160K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2596434	NM_015103.3(PLXND1):c.3018C>T (p.Leu1006=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related condition +1 more	GLikely benign
Select item 2595834	NM_015103.3(PLXND1):c.2627G>A (p.Arg876His)	PLXND1 (R876H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2588954	NM_015103.3(PLXND1):c.2458C>G (p.Gln820Glu)	PLXND1 (Q820E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2558320	NM_015103.3(PLXND1):c.4699A>G (p.Met1567Val)	PLXND1 (M1567V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2556402	NM_015103.3(PLXND1):c.4114G>T (p.Val1372Leu)	PLXND1 (V1372L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2555459	NM_015103.3(PLXND1):c.4207C>T (p.Arg1403Trp)	PLXND1 (R1403W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2551501	NM_015103.3(PLXND1):c.1829T>C (p.Ile610Thr)	PLXND1 (I610T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2547966	NM_015103.3(PLXND1):c.128G>A (p.Arg43Gln)	PLXND1 (R43Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2545828	NM_015103.3(PLXND1):c.2261G>A (p.Arg754Gln)	PLXND1 (R754Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2540146	NM_015103.3(PLXND1):c.4360G>A (p.Gly1454Ser)	PLXND1 (G1454S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2535823	NM_015103.3(PLXND1):c.8C>T (p.Pro3Leu)	PLXND1 (P3L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2534478	NM_015103.3(PLXND1):c.511G>C (p.Glu171Gln)	PLXND1 (E171Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2534477	NM_015103.3(PLXND1):c.485G>A (p.Arg162His)	PLXND1 (R162H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2531817	NM_015103.3(PLXND1):c.3325C>T (p.Arg1109Trp)	PLXND1 (R1109W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2527111	NM_015103.3(PLXND1):c.5548G>A (p.Glu1850Lys)	PLXND1 (E1850K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2519777	NM_015103.3(PLXND1):c.1643C>T (p.Ala548Val)	PLXND1 (A548V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2508154	NM_015103.3(PLXND1):c.2924G>A (p.Arg975His)	PLXND1 (R975H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2482017	NM_015103.3(PLXND1):c.4969A>G (p.Lys1657Glu)	PLXND1 (K1657E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2476059	NM_015103.3(PLXND1):c.3079C>G (p.Arg1027Gly)	PLXND1 (R1027G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2475870	NM_015103.3(PLXND1):c.455G>T (p.Arg152Leu)	PLXND1 (R152L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2465640	NM_015103.3(PLXND1):c.1720C>T (p.Arg574Trp)	PLXND1 (R574W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2458455	NM_015103.3(PLXND1):c.1453G>C (p.Val485Leu)	PLXND1 (V485L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2457063	NM_015103.3(PLXND1):c.3404C>T (p.Ala1135Val)	PLXND1 (A1135V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2445607	NM_015103.3(PLXND1):c.880_881del (p.Gln294fs)	PLXND1 (Q294fs)	Microsatellite (frameshift variant)	Congenital heart defects, multiple types, 9	GPathogenic
Select item 2445606	NM_015103.3(PLXND1):c.2733C>G (p.Ile911Met)	PLXND1 (I911M)	Single nucleotide variant (missense variant)	Congenital heart defects, multiple types, 9	GPathogenic

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