ClinVar for Gene (Select 91584) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3215583	NM_020911.2(PLXNA4):c.560C>T (p.Thr187Met)	PLXNA4 (T187M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215582	NM_020911.2(PLXNA4):c.229G>C (p.Asp77His)	PLXNA4 (D77H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215581	NM_020911.2(PLXNA4):c.1708G>A (p.Val570Ile)	PLXNA4 (V570I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215580	NM_020911.2(PLXNA4):c.1678C>T (p.Arg560Trp)	PLXNA4 (R560W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215579	NM_020911.2(PLXNA4):c.1605T>A (p.Thr535=)	PLXNA4	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3215578	NM_020911.2(PLXNA4):c.1415C>T (p.Thr472Met)	PLXNA4 (T472M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3062992	GRCh37/hg19 7q31.31-33(chr7:120582003-137699953)x1	AASS, AGBL3 +100 more	Copy number loss	not specified	GPathogenic
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 3061667	NM_020911.2(PLXNA4):c.5670G>A (p.Met1890Ile)	PLXNA4 (M1890I)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 3061642	NM_020911.2(PLXNA4):c.2812C>T (p.Arg938Trp)	PLXNA4 (R938W)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 3061637	NM_020911.2(PLXNA4):c.112C>T (p.Arg38Trp)	PLXNA4 (R38W)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 3061489	NM_020911.2(PLXNA4):c.840C>T (p.Leu280=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3061487	NM_020911.2(PLXNA4):c.1140G>A (p.Thr380=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3060996	NM_020911.2(PLXNA4):c.5613T>C (p.Asp1871=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GBenign
Select item 3060928	NM_020911.2(PLXNA4):c.5590-10C>T	PLXNA4	Single nucleotide variant (intron variant)	PLXNA4-related disorder	GBenign
Select item 3060616	NM_020911.2(PLXNA4):c.3876C>A (p.Ala1292=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GBenign
Select item 3060580	NM_020911.2(PLXNA4):c.504A>G (p.Ser168=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GBenign
Select item 3060134	NM_020911.2(PLXNA4):c.1815C>G (p.Val605=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GBenign
Select item 3059982	NM_020911.2(PLXNA4):c.3108T>C (p.Tyr1036=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GBenign
Select item 3059631	NM_020911.2(PLXNA4):c.1158C>T (p.Leu386=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GBenign
Select item 3059545	NM_020911.2(PLXNA4):c.3729A>G (p.Ala1243=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GBenign
Select item 3059115	NM_020911.2(PLXNA4):c.1372-87073A>G	PLXNA4 (M458V)	Single nucleotide variant (missense variant +1 more)	PLXNA4-related disorder	GBenign
Select item 3059070	NM_020911.2(PLXNA4):c.2211C>T (p.Tyr737=)	PLXNA4	Single nucleotide variant (synonymous 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 3057666	NM_020911.2(PLXNA4):c.3795C>T (p.Arg1265=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3057660	NM_020911.2(PLXNA4):c.2601A>G (p.Thr867=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3057375	NM_020911.2(PLXNA4):c.2246G>A (p.Arg749Gln)	PLXNA4 (R749Q)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 3056740	NM_020911.2(PLXNA4):c.2395+10_2395+23del	PLXNA4	Deletion (intron variant)	PLXNA4-related disorder	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 3055743	NM_020911.2(PLXNA4):c.2490C>A (p.Gly830=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3055333	NM_020911.2(PLXNA4):c.228C>T (p.Ser76=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GBenign
Select item 3055238	NM_020911.2(PLXNA4):c.1188+7A>G	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 3055192	NM_020911.2(PLXNA4):c.5475C>T (p.Ser1825=)	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 3055160	NM_020911.2(PLXNA4):c.4739G>T (p.Arg1580Leu)	PLXNA4 (R1580L)	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 3055062	NM_020911.2(PLXNA4):c.1371+4321A>C	PLXNA4 (I472L)	Single nucleotide variant (missense variant +1 more)	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 3054994	NM_020911.2(PLXNA4):c.5265G>A (p.Pro1755=)	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 3054978	NM_020911.2(PLXNA4):c.4425C>T (p.Asp1475=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
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 3054826	NM_020911.2(PLXNA4):c.1707C>T (p.Ser569=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3054811	NM_020911.2(PLXNA4):c.3123C>T (p.Thr1041=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3054700	NM_020911.2(PLXNA4):c.1371+4359T>C	PLXNA4	Single nucleotide variant (synonymous variant +1 more)	PLXNA4-related disorder	GLikely benign
Select item 3054665	NM_020911.2(PLXNA4):c.3126C>T (p.Ile1042=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3054598	NM_020911.2(PLXNA4):c.3875-7G>A	PLXNA4	Single nucleotide variant (intron 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 3054510	NM_020911.2(PLXNA4):c.3112G>C (p.Glu1038Gln)	PLXNA4 (E1038Q)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
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 3054495	NM_020911.2(PLXNA4):c.1108C>A (p.Arg370=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3054419	NM_020911.2(PLXNA4):c.1015T>A (p.Phe339Ile)	PLXNA4 (F339I)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 3054400	NM_020911.2(PLXNA4):c.1742C>T (p.Thr581Met)	PLXNA4 (T581M)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 3054332	NM_020911.2(PLXNA4):c.2952C>T (p.Asn984=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3054264	NM_020911.2(PLXNA4):c.2136G>A (p.Val712=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3054245	NM_020911.2(PLXNA4):c.1372-87037C>T	PLXNA4 (Q470*)	Single nucleotide variant (nonsense +1 more)	PLXNA4-related disorder	GUncertain significance
Select item 3054243	NM_020911.2(PLXNA4):c.5590-5C>T	PLXNA4	Single nucleotide variant (intron variant)	PLXNA4-related disorder	GLikely benign
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 3054191	NM_020911.2(PLXNA4):c.83G>A (p.Arg28Gln)	PLXNA4 (R28Q)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
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 3054085	NM_020911.2(PLXNA4):c.4434G>A (p.Thr1478=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3054062	NM_020911.2(PLXNA4):c.5590-4G>A	PLXNA4	Single nucleotide variant (intron variant)	PLXNA4-related disorder	GLikely benign
Select item 3054047	NM_020911.2(PLXNA4):c.2799C>T (p.Cys933=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3054022	NM_020911.2(PLXNA4):c.2670C>T (p.Ile890=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3053959	NM_020911.2(PLXNA4):c.1938C>T (p.Phe646=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3053915	NM_020911.2(PLXNA4):c.3303C>T (p.Leu1101=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3053906	NM_020911.2(PLXNA4):c.4500+6C>T	PLXNA4	Single nucleotide variant (intron variant)	PLXNA4-related disorder	GLikely benign
Select item 3053904	NM_020911.2(PLXNA4):c.2395+8A>T	PLXNA4	Single nucleotide variant (intron 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 3053716	NM_020911.2(PLXNA4):c.3177C>T (p.Ala1059=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3053566	NM_020911.2(PLXNA4):c.2463C>T (p.Phe821=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3052252	NM_020911.2(PLXNA4):c.1971C>T (p.Ser657=)	PLXNA4	Single nucleotide variant (synonymous 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 3052050	NM_020911.2(PLXNA4):c.3294G>T (p.Ala1098=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3051728	NM_020911.2(PLXNA4):c.2139C>A (p.Pro713=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
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 3051684	NM_020911.2(PLXNA4):c.80C>A (p.Thr27Asn)	PLXNA4 (T27N)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 3051673	NM_020911.2(PLXNA4):c.2587-3C>A	PLXNA4	Single nucleotide variant (intron variant)	PLXNA4-related disorder	GLikely benign
Select item 3051403	NM_020911.2(PLXNA4):c.3372C>T (p.Asn1124=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3051305	NM_020911.2(PLXNA4):c.2943C>T (p.Ala981=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3051296	NM_020911.2(PLXNA4):c.1371+8T>C	PLXNA4	Single nucleotide variant (intron variant)	PLXNA4-related disorder	GLikely benign
Select item 3051188	NM_020911.2(PLXNA4):c.1008C>T (p.Phe336=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3051080	NM_020911.2(PLXNA4):c.1371+4431G>A	PLXNA4	Single nucleotide variant (synonymous variant +1 more)	PLXNA4-related disorder	GLikely benign
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 3049591	NM_020911.2(PLXNA4):c.649G>A (p.Val217Ile)	PLXNA4 (V217I)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
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 3049247	NM_020911.2(PLXNA4):c.1372-87013G>A	PLXNA4 (A478T)	Single nucleotide variant (missense variant +1 more)	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 3049032	NM_020911.2(PLXNA4):c.119T>C (p.Phe40Ser)	PLXNA4 (F40S)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GLikely benign
Select item 3048985	NM_020911.2(PLXNA4):c.3319C>T (p.His1107Tyr)	PLXNA4 (H1107Y)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
Select item 3048889	NM_020911.2(PLXNA4):c.645G>A (p.Ala215=)	PLXNA4	Single nucleotide variant (synonymous 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 3048531	NM_020911.2(PLXNA4):c.441C>T (p.Phe147=)	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 3048342	NM_020911.2(PLXNA4):c.3760G>A (p.Val1254Met)	PLXNA4 (V1254M)	Single nucleotide variant (missense variant)	PLXNA4-related disorder	GUncertain significance
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 3048000	NM_020911.2(PLXNA4):c.1372-86990G>A	PLXNA4	Single nucleotide variant (synonymous variant +1 more)	PLXNA4-related disorder	GLikely benign
Select item 3047774	NM_020911.2(PLXNA4):c.2655G>A (p.Leu885=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign
Select item 3047684	NM_020911.2(PLXNA4):c.264G>A (p.Pro88=)	PLXNA4	Single nucleotide variant (synonymous variant)	PLXNA4-related disorder	GLikely benign

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