PLXNA3[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3355805	NM_017514.5(PLXNA3):c.-7G>A	PLXNA3	Single nucleotide variant (5 prime UTR variant)	PLXNA3-related disorder	GLikely benign
Select item 3055450	NM_017514.5(PLXNA3):c.-5C>T	PLXNA3	Single nucleotide variant (5 prime UTR variant)	PLXNA3-related disorder	GLikely benign
Select item 3036482	NM_017514.5(PLXNA3):c.-4G>A	PLXNA3	Single nucleotide variant (5 prime UTR variant)	PLXNA3-related disorder	GLikely benign
Select item 3357869	NM_017514.5(PLXNA3):c.10G>C (p.Val4Leu)	PLXNA3 (V4L)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GUncertain significance
Select item 777847	NM_017514.5(PLXNA3):c.12C>G (p.Val4=)	PLXNA3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3046831	NM_017514.5(PLXNA3):c.18C>T (p.Leu6=)	PLXNA3	Single nucleotide variant (synonymous variant)	PLXNA3-related disorder	GLikely benign
Select item 3355247	NM_017514.5(PLXNA3):c.19C>T (p.Leu7Phe)	PLXNA3 (L7F)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GUncertain significance
Select item 3054656	NM_017514.5(PLXNA3):c.39C>T (p.Ala13=)	PLXNA3	Single nucleotide variant (synonymous variant)	PLXNA3-related disorder	GLikely benign
Select item 2539620	NM_017514.5(PLXNA3):c.40G>A (p.Val14Met)	PLXNA3 (V14M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3050066	NM_017514.5(PLXNA3):c.49dup (p.Ala17fs)	PLXNA3 (A17fs)	Duplication (frameshift variant)	PLXNA3-related disorder	GUncertain significance
Select item 3030538	NM_017514.5(PLXNA3):c.42G>C (p.Val14=)	PLXNA3	Single nucleotide variant (synonymous variant)	PLXNA3-related disorder	GLikely benign
Select item 3349899	NM_017514.5(PLXNA3):c.43G>C (p.Gly15Arg)	PLXNA3 (G15R)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GUncertain significance
Select item 3355653	NM_017514.5(PLXNA3):c.45G>A (p.Gly15=)	PLXNA3	Single nucleotide variant (synonymous variant)	PLXNA3-related disorder	GLikely benign
Select item 3351262	NM_017514.5(PLXNA3):c.48G>T (p.Gly16=)	PLXNA3	Single nucleotide variant (synonymous variant)	PLXNA3-related disorder	GLikely benign
Select item 2358147	NM_017514.5(PLXNA3):c.55G>A (p.Gly19Ser)	PLXNA3 (G19S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 599563	NM_017514.5(PLXNA3):c.56G>A (p.Gly19Asp)	PLXNA3 (G19D)	Single nucleotide variant (missense variant)	not specified	GConflicting classifications of pathogenicity
Select item 3307913	NM_017514.5(PLXNA3):c.70C>T (p.Arg24Cys)	PLXNA3 (R24C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 720976	NM_017514.5(PLXNA3):c.71G>A (p.Arg24His)	PLXNA3 (R24H)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3047370	NM_017514.5(PLXNA3):c.78C>T (p.Phe26=)	PLXNA3	Single nucleotide variant (synonymous variant)	PLXNA3-related disorder	GLikely benign
Select item 2401729	NM_017514.5(PLXNA3):c.79G>A (p.Val27Met)	PLXNA3 (V27M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209281	NM_017514.5(PLXNA3):c.95C>T (p.Thr32Met)	PLXNA3 (T32M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3348952	NM_017514.5(PLXNA3):c.105C>G (p.His35Gln)	PLXNA3 (H35Q)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GUncertain significance
Select item 3356549	NM_017514.5(PLXNA3):c.118C>T (p.Arg40Trp)	PLXNA3 (R40W)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GUncertain significance
Select item 2632133	NM_017514.5(PLXNA3):c.119G>A (p.Arg40Gln)	PLXNA3 (R40Q)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GUncertain significance
Select item 3348554	NM_017514.5(PLXNA3):c.124A>T (p.Thr42Ser)	PLXNA3 (T42S)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GUncertain significance
Select item 3351231	NM_017514.5(PLXNA3):c.133G>A (p.Val45Met)	PLXNA3 (V45M)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GLikely benign
Select item 749131	NM_017514.5(PLXNA3):c.138C>T (p.Phe46=)	PLXNA3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2661820	NM_017514.5(PLXNA3):c.144C>T (p.Gly48=)	PLXNA3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3347978	NM_017514.5(PLXNA3):c.145G>A (p.Ala49Thr)	PLXNA3 (A49T)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GUncertain significance
Select item 3344735	NM_017514.5(PLXNA3):c.154C>G (p.Arg52Gly)	PLXNA3 (R52G)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GUncertain significance
Select item 2629248	NM_017514.5(PLXNA3):c.166C>G (p.Leu56Val)	PLXNA3 (L56V)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GUncertain significance
Select item 3355447	NM_017514.5(PLXNA3):c.170C>T (p.Ala57Val)	PLXNA3 (A57V)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GUncertain significance
Select item 3348372	NM_017514.5(PLXNA3):c.170C>A (p.Ala57Asp)	PLXNA3 (A57D)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GUncertain significance
Select item 773622	NM_017514.5(PLXNA3):c.172C>T (p.Pro58Ser)	PLXNA3 (P58S)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 3348542	NM_017514.5(PLXNA3):c.182C>G (p.Thr61Ser)	PLXNA3 (T61S)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GUncertain significance
Select item 3047173	NM_017514.5(PLXNA3):c.187C>G (p.Leu63Val)	PLXNA3 (L63V)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GLikely benign
Select item 3048878	NM_017514.5(PLXNA3):c.190C>T (p.Arg64Trp)	PLXNA3 (R64W)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GLikely benign
Select item 2661821	NM_017514.5(PLXNA3):c.196C>T (p.His66Tyr)	PLXNA3 (H66Y)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3358054	NM_017514.5(PLXNA3):c.202A>G (p.Thr68Ala)	PLXNA3 (T68A)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GUncertain significance
Select item 3358548	NM_017514.5(PLXNA3):c.203C>T (p.Thr68Met)	PLXNA3 (T68M)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GUncertain significance
Select item 3048627	NM_017514.5(PLXNA3):c.210C>T (p.Pro70=)	PLXNA3	Single nucleotide variant (synonymous variant)	PLXNA3-related disorder	GLikely benign
Select item 3037082	NM_017514.5(PLXNA3):c.213C>T (p.Val71=)	PLXNA3	Single nucleotide variant (synonymous variant)	PLXNA3-related disorder	GLikely benign
Select item 417914	NM_017514.5(PLXNA3):c.214G>A (p.Glu72Lys)	PLXNA3 (E72K)	Single nucleotide variant (missense variant)	Autism +1 more	GUncertain significance
Select item 3051522	NM_017514.5(PLXNA3):c.222C>T (p.Asn74=)	PLXNA3	Single nucleotide variant (synonymous variant)	PLXNA3-related disorder	GLikely benign
Select item 2383673	NM_017514.5(PLXNA3):c.226C>T (p.Arg76Cys)	PLXNA3 (R76C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3032501	NM_017514.5(PLXNA3):c.237G>A (p.Pro79=)	PLXNA3	Single nucleotide variant (synonymous variant)	PLXNA3-related disorder	GLikely benign
Select item 3215556	NM_017514.5(PLXNA3):c.238C>G (p.Pro80Ala)	PLXNA3 (P80A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2634363	NM_017514.5(PLXNA3):c.241C>G (p.Pro81Ala)	PLXNA3 (P81A)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GUncertain significance
Select item 3348459	NM_017514.5(PLXNA3):c.242C>G (p.Pro81Arg)	PLXNA3 (P81R)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GUncertain significance
Select item 2661822	NM_017514.5(PLXNA3):c.252C>T (p.Arg84=)	PLXNA3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2634490	NM_017514.5(PLXNA3):c.252C>G (p.Arg84=)	PLXNA3	Single nucleotide variant (synonymous variant)	PLXNA3-related disorder	GUncertain significance
Select item 3356568	NM_017514.5(PLXNA3):c.253G>A (p.Val85Met)	PLXNA3 (V85M)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GUncertain significance
Select item 2636891	NM_017514.5(PLXNA3):c.262C>T (p.His88Tyr)	PLXNA3 (H88Y)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GUncertain significance
Select item 727527	NM_017514.5(PLXNA3):c.266G>A (p.Arg89His)	PLXNA3 (R89H)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3352049	NM_017514.5(PLXNA3):c.267C>G (p.Arg89=)	PLXNA3	Single nucleotide variant (synonymous variant)	PLXNA3-related disorder	GLikely benign
Select item 3354539	NM_017514.5(PLXNA3):c.270G>A (p.Leu90=)	PLXNA3	Single nucleotide variant (synonymous variant)	PLXNA3-related disorder	GLikely benign
Select item 3030281	NM_017514.5(PLXNA3):c.272C>T (p.Ala91Val)	PLXNA3 (A91V)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GLikely benign
Select item 3042417	NM_017514.5(PLXNA3):c.276C>T (p.Pro92=)	PLXNA3	Single nucleotide variant (synonymous variant)	PLXNA3-related disorder	GLikely benign
Select item 3215558	NM_017514.5(PLXNA3):c.277G>A (p.Val93Met)	PLXNA3 (V93M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3029439	NM_017514.5(PLXNA3):c.295C>G (p.Leu99Val)	PLXNA3 (L99V)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GUncertain significance
Select item 3355159	NM_017514.5(PLXNA3):c.300G>A (p.Leu100=)	PLXNA3	Single nucleotide variant (synonymous variant)	PLXNA3-related disorder	GLikely benign
Select item 3215562	NM_017514.5(PLXNA3):c.304A>G (p.Ile102Val)	PLXNA3 (I102V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3045765	NM_017514.5(PLXNA3):c.312T>C (p.Tyr104=)	PLXNA3	Single nucleotide variant (synonymous variant)	PLXNA3-related disorder	GLikely benign
Select item 2634988	NM_017514.5(PLXNA3):c.314C>T (p.Ala105Val)	PLXNA3 (A105V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3041028	NM_017514.5(PLXNA3):c.315G>A (p.Ala105=)	PLXNA3	Single nucleotide variant (synonymous variant)	PLXNA3-related disorder	GLikely benign
Select item 3045505	NM_017514.5(PLXNA3):c.319C>T (p.Arg107Cys)	PLXNA3 (R107C)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GLikely benign
Select item 727176	NM_017514.5(PLXNA3):c.320G>A (p.Arg107His)	PLXNA3 (R107H)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 982252	NM_017514.5(PLXNA3):c.322C>T (p.Arg108Cys)	PLXNA3 (R108C)	Single nucleotide variant (missense variant)	Hypogonadotropic hypogonadism	GUncertain significance
Select item 3036965	NM_017514.5(PLXNA3):c.336C>T (p.Cys112=)	PLXNA3	Single nucleotide variant (synonymous variant)	PLXNA3-related disorder	GLikely benign
Select item 2359122	NM_017514.5(PLXNA3):c.341G>C (p.Ser114Thr)	PLXNA3 (S114T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215563	NM_017514.5(PLXNA3):c.357C>G (p.Ile119Met)	PLXNA3 (I119M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2661823	NM_017514.5(PLXNA3):c.370C>T (p.Arg124Cys)	PLXNA3 (R124C)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2461871	NM_017514.5(PLXNA3):c.371G>A (p.Arg124His)	PLXNA3 (R124H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3356237	NM_017514.5(PLXNA3):c.384C>T (p.Leu128=)	PLXNA3	Single nucleotide variant (synonymous variant)	PLXNA3-related disorder	GLikely benign
Select item 3056075	NM_017514.5(PLXNA3):c.391C>T (p.Leu131=)	PLXNA3	Single nucleotide variant (synonymous variant)	PLXNA3-related disorder	GLikely benign
Select item 741242	NM_017514.5(PLXNA3):c.402G>A (p.Pro134=)	PLXNA3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2635998	NM_017514.5(PLXNA3):c.409C>T (p.Arg137Cys)	PLXNA3 (R137C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3351041	NM_017514.5(PLXNA3):c.410G>A (p.Arg137His)	PLXNA3 (R137H)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GUncertain significance
Select item 3357593	NM_017514.5(PLXNA3):c.421T>C (p.Tyr141His)	PLXNA3 (Y141H)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GUncertain significance
Select item 2230015	NM_017514.5(PLXNA3):c.431G>T (p.Gly144Val)	PLXNA3 (G144V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554211	NM_017514.5(PLXNA3):c.434C>A (p.Ala145Asp)	PLXNA3 (A145D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3030044	NM_017514.5(PLXNA3):c.435C>T (p.Ala145=)	PLXNA3	Single nucleotide variant (synonymous variant)	PLXNA3-related disorder	GLikely benign
Select item 3349299	NM_017514.5(PLXNA3):c.437A>G (p.Gln146Arg)	PLXNA3 (Q146R)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GUncertain significance
Select item 3048174	NM_017514.5(PLXNA3):c.444C>T (p.Pro148=)	PLXNA3	Single nucleotide variant (synonymous variant)	PLXNA3-related disorder	GLikely benign
Select item 3355068	NM_017514.5(PLXNA3):c.445G>A (p.Asp149Asn)	PLXNA3 (D149N)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GUncertain significance
Select item 2661824	NM_017514.5(PLXNA3):c.447C>T (p.Asp149=)	PLXNA3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3353931	NM_017514.5(PLXNA3):c.448T>G (p.Ser150Ala)	PLXNA3 (S150A)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GUncertain significance
Select item 3051286	NM_017514.5(PLXNA3):c.459T>C (p.Gly153=)	PLXNA3	Single nucleotide variant (synonymous variant)	PLXNA3-related disorder	GLikely benign
Select item 3032114	NM_017514.5(PLXNA3):c.513C>T (p.Val171=)	PLXNA3	Single nucleotide variant (synonymous variant)	PLXNA3-related disorder	GLikely benign
Select item 2509783	NM_017514.5(PLXNA3):c.514G>A (p.Asp172Asn)	PLXNA3 (D172N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2661825	NM_017514.5(PLXNA3):c.516C>T (p.Asp172=)	PLXNA3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3358596	NM_017514.5(PLXNA3):c.517G>A (p.Gly173Ser)	PLXNA3 (G173S)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GUncertain significance
Select item 2354726	NM_017514.5(PLXNA3):c.524C>T (p.Ser175Leu)	PLXNA3 (S175L)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3349715	NM_017514.5(PLXNA3):c.540C>G (p.Thr180=)	PLXNA3	Single nucleotide variant (synonymous variant)	PLXNA3-related disorder	GLikely benign
Select item 3061509	NM_017514.5(PLXNA3):c.549C>A (p.Ser183=)	PLXNA3	Single nucleotide variant (synonymous variant)	PLXNA3-related disorder	GLikely benign
Select item 3355473	NM_017514.5(PLXNA3):c.552C>G (p.Arg184=)	PLXNA3	Single nucleotide variant (synonymous variant)	PLXNA3-related disorder	GLikely benign
Select item 3345642	NM_017514.5(PLXNA3):c.572A>G (p.Asp191Gly)	PLXNA3 (D191G)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GUncertain significance
Select item 3348217	NM_017514.5(PLXNA3):c.575G>T (p.Ser192Ile)	PLXNA3 (S192I)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GUncertain significance
Select item 3038660	NM_017514.5(PLXNA3):c.576C>T (p.Ser192=)	PLXNA3	Single nucleotide variant (synonymous variant)	PLXNA3-related disorder	GLikely benign
Select item 3047184	NM_017514.5(PLXNA3):c.578C>T (p.Ala193Val)	PLXNA3 (A193V)	Single nucleotide variant (missense variant)	PLXNA3-related disorder	GLikely benign

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