"PLXNA4-related disorder"[Disease/phenotype] AND "PreventionGenetics, - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3035988	NM_020911.2(PLXNA4):c.*6G>A	PLXNA4	Single nucleotide variant (3 prime UTR variant)	PLXNA4-related disorder	GLikely benign
Select item 3036086	NM_020911.2(PLXNA4):c.*5C>T	PLXNA4	Single nucleotide variant (3 prime UTR variant)	PLXNA4-related disorder	GLikely benign
Select item 3061667	NM_020911.2(PLXNA4):c.5670G>A (p.Met1890Ile)	PLXNA4 (M1890I)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 3031942	NM_020911.2(PLXNA4):c.5649A>C (p.Leu1883=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3044029	NM_020911.2(PLXNA4):c.5636T>G (p.Leu1879Arg)	PLXNA4 (L1879R)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 3060996	NM_020911.2(PLXNA4):c.5613T>C (p.Asp1871=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GBenign
Select item 2634045	NM_020911.2(PLXNA4):c.5611G>A (p.Asp1871Asn)	PLXNA4 (D1871N)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 3041401	NM_020911.2(PLXNA4):c.5608C>T (p.His1870Tyr)	PLXNA4 (H1870Y)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GBenign
Select item 3054062	NM_020911.2(PLXNA4):c.5590-4G>A	PLXNA4	Single nucleotide variant (intron variant)	PLXNA4-related disorder	GLikely benign
Select item 3054243	NM_020911.2(PLXNA4):c.5590-5C>T	PLXNA4	Single nucleotide variant (intron variant)	PLXNA4-related disorder	GLikely benign
Select item 3060928	NM_020911.2(PLXNA4):c.5590-10C>T	PLXNA4	Single nucleotide variant (intron variant)	PLXNA4-related disorder	GBenign
Select item 3041340	NM_020911.2(PLXNA4):c.5574C>A (p.Gly1858=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3048341	NM_020911.2(PLXNA4):c.5564C>T (p.Ser1855Phe)	PLXNA4 (S1855F)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GLikely benign
Select item 3059020	NM_020911.2(PLXNA4):c.5547A>G (p.Ala1849=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GBenign
Select item 2635717	NM_020911.2(PLXNA4):c.5539A>G (p.Met1847Val)	PLXNA4 (M1847V)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 3032706	NM_020911.2(PLXNA4):c.5513G>A (p.Arg1838Gln)	PLXNA4 (R1838Q)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 3031715	NM_020911.2(PLXNA4):c.5490C>T (p.Asn1830=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3055192	NM_020911.2(PLXNA4):c.5475C>T (p.Ser1825=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3029697	NM_020911.2(PLXNA4):c.5363G>A (p.Arg1788Gln)	PLXNA4 (R1788Q)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 3054916	NM_020911.2(PLXNA4):c.5352G>T (p.Thr1784=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3048442	NM_020911.2(PLXNA4):c.5304C>T (p.Asp1768=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3054994	NM_020911.2(PLXNA4):c.5265G>A (p.Pro1755=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3054566	NM_020911.2(PLXNA4):c.5226-4G>A	PLXNA4	Single nucleotide variant (intron variant)	PLXNA4-related disorder	GLikely benign
Select item 3052136	NM_020911.2(PLXNA4):c.5226-5C>T	PLXNA4	Single nucleotide variant (intron variant)	PLXNA4-related disorder	GLikely benign
Select item 2636586	NM_020911.2(PLXNA4):c.5200G>A (p.Val1734Ile)	PLXNA4 (V1734I)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 3049098	NM_020911.2(PLXNA4):c.5199C>T (p.His1733=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3054509	NM_020911.2(PLXNA4):c.5196G>A (p.Pro1732=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3031618	NM_020911.2(PLXNA4):c.4980C>T (p.His1660=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 713226	NM_020911.2(PLXNA4):c.4974C>T (p.His1658=)	PLXNA4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2632070	NM_020911.2(PLXNA4):c.4927C>A (p.Pro1643Thr)	PLXNA4 (P1643T)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 2628924	NM_020911.2(PLXNA4):c.4903C>T (p.Arg1635Cys)	PLXNA4 (R1635C)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 2636534	NM_020911.2(PLXNA4):c.4870A>G (p.Met1624Val)	PLXNA4 (M1624V)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 2634396	NM_020911.2(PLXNA4):c.4819G>A (p.Ala1607Thr)	PLXNA4 (A1607T)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 2634533	NM_020911.2(PLXNA4):c.4780G>A (p.Val1594Met)	PLXNA4 (V1594M)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 3032172	NM_020911.2(PLXNA4):c.4779C>T (p.Ser1593=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3032645	NM_020911.2(PLXNA4):c.4776T>C (p.Gly1592=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3055061	NM_020911.2(PLXNA4):c.4749A>G (p.Thr1583=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3055160	NM_020911.2(PLXNA4):c.4739G>T (p.Arg1580Leu)	PLXNA4 (R1580L)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 2636670	NM_020911.2(PLXNA4):c.4739G>A (p.Arg1580Gln)	PLXNA4 (R1580Q)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 3061699	NM_020911.2(PLXNA4):c.4737G>A (p.Lys1579=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 2634208	NM_020911.2(PLXNA4):c.4721T>C (p.Ile1574Thr)	PLXNA4 (I1574T)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 2636098	NM_020911.2(PLXNA4):c.4676G>A (p.Ser1559Asn)	PLXNA4 (S1559N)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 2628652	NM_020911.2(PLXNA4):c.4667G>A (p.Arg1556Gln)	PLXNA4 (R1556Q)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 2635065	NM_020911.2(PLXNA4):c.4633C>T (p.Arg1545Trp)	PLXNA4 (R1545W)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 2634729	NM_020911.2(PLXNA4):c.4540G>A (p.Glu1514Lys)	PLXNA4 (E1514K)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 3045449	NM_020911.2(PLXNA4):c.4539C>T (p.Pro1513=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 770744	NM_020911.2(PLXNA4):c.4500+8C>T	PLXNA4	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 3053906	NM_020911.2(PLXNA4):c.4500+6C>T	PLXNA4	Single nucleotide variant (intron variant)	PLXNA4-related disorder	GLikely benign
Select item 3048817	NM_020911.2(PLXNA4):c.4458C>T (p.Ser1486=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3055173	NM_020911.2(PLXNA4):c.4437C>T (p.Gly1479=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3054085	NM_020911.2(PLXNA4):c.4434G>A (p.Thr1478=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3054978	NM_020911.2(PLXNA4):c.4425C>T (p.Asp1475=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3029748	NM_020911.2(PLXNA4):c.4293G>A (p.Glu1431=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3047502	NM_020911.2(PLXNA4):c.4286+10C>T	PLXNA4	Single nucleotide variant (intron variant)	PLXNA4-related disorder	GLikely benign
Select item 2629514	NM_020911.2(PLXNA4):c.4278G>C (p.Leu1426=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3035916	NM_020911.2(PLXNA4):c.4230C>T (p.Ala1410=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3054979	NM_020911.2(PLXNA4):c.4200C>T (p.Tyr1400=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3036239	NM_020911.2(PLXNA4):c.4176C>T (p.Thr1392=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 2635777	NM_020911.2(PLXNA4):c.4156G>A (p.Val1386Met)	PLXNA4 (V1386M)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 3046111	NM_020911.2(PLXNA4):c.4144G>A (p.Asp1382Asn)	PLXNA4 (D1382N)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 2629409	NM_020911.2(PLXNA4):c.4067C>A (p.Ala1356Asp)	PLXNA4 (A1356D)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 3055136	NM_020911.2(PLXNA4):c.4065C>T (p.Phe1355=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3049466	NM_020911.2(PLXNA4):c.4040G>A (p.Arg1347His)	PLXNA4 (R1347H)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 3054195	NM_020911.2(PLXNA4):c.4031G>A (p.Arg1344Gln)	PLXNA4 (R1344Q)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 2635944	NM_020911.2(PLXNA4):c.4022C>T (p.Pro1341Leu)	PLXNA4 (P1341L)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 2635311	NM_020911.2(PLXNA4):c.3966G>T (p.Met1322Ile)	PLXNA4 (M1322I)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 3037107	NM_020911.2(PLXNA4):c.3930C>T (p.Ala1310=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3054099	NM_020911.2(PLXNA4):c.3882C>T (p.Ala1294=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3060616	NM_020911.2(PLXNA4):c.3876C>A (p.Ala1292=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GBenign
Select item 3054598	NM_020911.2(PLXNA4):c.3875-7G>A	PLXNA4	Single nucleotide variant (intron variant)	PLXNA4-related disorder	GLikely benign
Select item 3055193	NM_020911.2(PLXNA4):c.3875-8C>T	PLXNA4	Single nucleotide variant (intron variant)	PLXNA4-related disorder	GLikely benign
Select item 3057666	NM_020911.2(PLXNA4):c.3795C>T (p.Arg1265=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 2635708	NM_020911.2(PLXNA4):c.3794G>A (p.Arg1265His)	PLXNA4 (R1265H)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 2634424	NM_020911.2(PLXNA4):c.3785G>A (p.Arg1262His)	PLXNA4 (R1262H)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 3048342	NM_020911.2(PLXNA4):c.3760G>A (p.Val1254Met)	PLXNA4 (V1254M)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 2629572	NM_020911.2(PLXNA4):c.3745C>A (p.Leu1249Ile)	PLXNA4 (L1249I)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 2634880	NM_020911.2(PLXNA4):c.3739G>A (p.Gly1247Ser)	PLXNA4 (G1247S)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 3036064	NM_020911.2(PLXNA4):c.3738C>T (p.Gly1246=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3059545	NM_020911.2(PLXNA4):c.3729A>G (p.Ala1243=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GBenign
Select item 2634822	NM_020911.2(PLXNA4):c.3727G>A (p.Ala1243Thr)	PLXNA4 (A1243T)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 3050948	NM_020911.2(PLXNA4):c.3711C>T (p.Pro1237=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3036610	NM_020911.2(PLXNA4):c.3705C>T (p.Ser1235=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3029701	NM_020911.2(PLXNA4):c.3702C>T (p.Leu1234=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3038811	NM_020911.2(PLXNA4):c.3693C>A (p.Asp1231Glu)	PLXNA4 (D1231E)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GLikely benign
Select item 2634868	NM_020911.2(PLXNA4):c.3689C>A (p.Pro1230Gln)	PLXNA4 (P1230Q)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 3041578	NM_020911.2(PLXNA4):c.3663C>T (p.Tyr1221=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3046628	NM_020911.2(PLXNA4):c.3644G>A (p.Arg1215His)	PLXNA4 (R1215H)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 3051709	NM_020911.2(PLXNA4):c.3579C>T (p.Thr1193=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 720132	NM_020911.2(PLXNA4):c.3567G>A (p.Pro1189=)	PLXNA4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3031959	NM_020911.2(PLXNA4):c.3537G>A (p.Leu1179=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3038704	NM_020911.2(PLXNA4):c.3528C>T (p.Asn1176=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3044027	NM_020911.2(PLXNA4):c.3511C>T (p.Pro1171Ser)	PLXNA4 (P1171S)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GLikely benign
Select item 3030348	NM_020911.2(PLXNA4):c.3510G>A (p.Pro1170=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3053890	NM_020911.2(PLXNA4):c.3493-7T>C	PLXNA4	Single nucleotide variant (intron variant)	PLXNA4-related disorder	GLikely benign
Select item 3038370	NM_020911.2(PLXNA4):c.3492+9A>T	PLXNA4	Single nucleotide variant (intron variant)	PLXNA4-related disorder	GLikely benign
Select item 3038006	NM_020911.2(PLXNA4):c.3492+5A>T	PLXNA4	Single nucleotide variant (intron variant)	PLXNA4-related disorder	GLikely benign
Select item 3032899	NM_020911.2(PLXNA4):c.3492+3G>A	PLXNA4	Single nucleotide variant (intron variant)	PLXNA4-related disorder	GLikely benign
Select item 780720	NM_020911.2(PLXNA4):c.3477G>A (p.Thr1159=)	PLXNA4	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3056319	NM_020911.2(PLXNA4):c.3426G>A (p.Pro1142=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GBenign
Select item 3028942	NM_020911.2(PLXNA4):c.3384G>C (p.Leu1128=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign

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