"PreventionGenetics, part of Exact Sciences"[submitter] AND "PLXND1"[g - ClinVar

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Items: 60

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3059889	NM_015103.3(PLXND1):c.5727G>A (p.Gln1909=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related disorder	GBenign
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 3033777	NM_015103.3(PLXND1):c.5640C>T (p.Tyr1880=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related disorder	GLikely benign
Select item 722559	NM_015103.3(PLXND1):c.5446-10CT[4]	PLXND1	Microsatellite (intron variant)	not provided +1 more	GLikely benign
Select item 708884	NM_015103.3(PLXND1):c.5032C>A (p.Leu1678Met)	PLXND1 (L1678M)	Single nucleotide variant (missense variant)	PLXND1-related disorder +1 more	GBenign
Select item 3060610	NM_015103.3(PLXND1):c.4994-4A>G	PLXND1	Single nucleotide variant (intron variant)	PLXND1-related disorder	GBenign
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 730293	NM_015103.3(PLXND1):c.4803G>A (p.Pro1601=)	PLXND1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1183583	NM_015103.3(PLXND1):c.4737G>A (p.Thr1579=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related disorder +1 more	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 3044790	NM_015103.3(PLXND1):c.4311G>A (p.Ala1437=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related disorder	GLikely benign
Select item 1230209	NM_015103.3(PLXND1):c.4234T>G (p.Leu1412Val)	PLXND1 (L1412V)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 2654127	NM_015103.3(PLXND1):c.4086+8C>T	PLXND1	Single nucleotide variant (intron variant)	PLXND1-related disorder +1 more	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 3060110	NM_015103.3(PLXND1):c.3973+10G>T	PLXND1	Single nucleotide variant (intron variant)	PLXND1-related disorder	GBenign
Select item 3060694	NM_015103.3(PLXND1):c.3879C>T (p.Phe1293=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related disorder	GBenign
Select item 784603	NM_015103.3(PLXND1):c.3866-4G>A	PLXND1	Single nucleotide variant (intron variant)	PLXND1-related disorder +1 more	GLikely benign
Select item 723284	NM_015103.3(PLXND1):c.3641G>A (p.Arg1214Gln)	PLXND1 (R1214Q)	Single nucleotide variant (missense variant)	not provided +1 more	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 779416	NM_015103.3(PLXND1):c.3505C>T (p.Arg1169Cys)	PLXND1 (R1169C)	Single nucleotide variant (missense variant)	not provided +1 more	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 733952	NM_015103.3(PLXND1):c.3448G>T (p.Val1150Leu)	PLXND1 (V1150L)	Single nucleotide variant (missense variant)	PLXND1-related disorder +1 more	GBenign/Likely benign
Select item 722180	NM_015103.3(PLXND1):c.3444C>T (p.Asp1148=)	PLXND1	Single nucleotide variant (synonymous variant)	not provided +1 more	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 3055934	NM_015103.3(PLXND1):c.3030C>T (p.Ser1010=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related disorder	GBenign
Select item 2596434	NM_015103.3(PLXND1):c.3018C>T (p.Leu1006=)	PLXND1	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 731022	NM_015103.3(PLXND1):c.2937+10G>T	PLXND1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 771352	NM_015103.3(PLXND1):c.2918G>A (p.Arg973Gln)	PLXND1 (R973Q)	Single nucleotide variant (missense variant)	PLXND1-related disorder +1 more	GBenign
Select item 1230863	NM_015103.3(PLXND1):c.2871A>G (p.Pro957=)	PLXND1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 716851	NM_015103.3(PLXND1):c.2829G>A (p.Val943=)	PLXND1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 712440	NM_015103.3(PLXND1):c.2712C>T (p.Asp904=)	PLXND1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 720178	NM_015103.3(PLXND1):c.2610G>A (p.Met870Ile)	PLXND1 (M870I)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
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 744242	NM_015103.3(PLXND1):c.2548G>A (p.Ala850Thr)	PLXND1 (A850T)	Single nucleotide variant (missense variant)	PLXND1-related disorder +1 more	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 789278	NM_015103.3(PLXND1):c.2275C>T (p.Pro759Ser)	PLXND1 (P759S)	Single nucleotide variant (missense variant)	PLXND1-related disorder +1 more	GBenign
Select item 773447	NM_015103.3(PLXND1):c.2263A>G (p.Thr755Ala)	PLXND1 (T755A)	Single nucleotide variant (missense variant)	PLXND1-related disorder +2 more	GBenign/Likely benign
Select item 3055313	NM_015103.3(PLXND1):c.2196C>T (p.Ser732=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related disorder	GBenign
Select item 712509	NM_015103.3(PLXND1):c.2162A>G (p.Gln721Arg)	PLXND1 (Q721R)	Single nucleotide variant (missense variant)	not provided +1 more	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 733602	NM_015103.3(PLXND1):c.1980C>T (p.Tyr660=)	PLXND1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
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 3034585	NM_015103.3(PLXND1):c.1845G>A (p.Glu615=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related disorder	GLikely benign
Select item 723395	NM_015103.3(PLXND1):c.1795C>T (p.Arg599Cys)	PLXND1 (R599C)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 717202	NM_015103.3(PLXND1):c.1698C>T (p.Cys566=)	PLXND1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 744934	NM_015103.3(PLXND1):c.1650C>T (p.Asn550=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related disorder +1 more	GLikely benign
Select item 720179	NM_015103.3(PLXND1):c.1641C>T (p.Ala547=)	PLXND1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 724204	NM_015103.3(PLXND1):c.1592G>T (p.Gly531Val)	PLXND1 (G531V)	Single nucleotide variant (missense variant)	not provided +1 more	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 2654128	NM_015103.3(PLXND1):c.1578C>G (p.Asp526Glu)	PLXND1 (D526E)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 716852	NM_015103.3(PLXND1):c.1513G>C (p.Val505Leu)	PLXND1 (V505L)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 726949	NM_015103.3(PLXND1):c.1511A>G (p.Gln504Arg)	PLXND1 (Q504R)	Single nucleotide variant (missense variant)	PLXND1-related disorder +1 more	GBenign
Select item 782243	NM_015103.3(PLXND1):c.1501G>A (p.Glu501Lys)	PLXND1 (E501K)	Single nucleotide variant (missense variant)	not provided +1 more	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 708070	NM_015103.3(PLXND1):c.1350G>A (p.Leu450=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related disorder +1 more	GLikely benign
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 736752	NM_015103.3(PLXND1):c.847T>C (p.Phe283Leu)	PLXND1 (F283L)	Single nucleotide variant (missense variant)	PLXND1-related disorder +1 more	GBenign/Likely benign
Select item 791248	NM_015103.3(PLXND1):c.780C>G (p.Ser260=)	PLXND1	Single nucleotide variant (synonymous variant)	PLXND1-related disorder +1 more	GBenign/Likely 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

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Items: 60