ClinVar for Gene (Select 5361) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3358837	NM_032242.4(PLXNA1):c.5644C>T (p.Arg1882Trp)	PLXNA1 (R1882W)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3358797	NM_032242.4(PLXNA1):c.3148A>G (p.Ile1050Val)	PLXNA1 (I1050V)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3358731	NM_032242.4(PLXNA1):c.3576C>T (p.Ile1192=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3358703	NM_032242.4(PLXNA1):c.1333C>T (p.Arg445Cys)	PLXNA1 (R445C)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3358695	NM_032242.4(PLXNA1):c.4947C>T (p.Ser1649=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3358677	NM_032242.4(PLXNA1):c.2373C>T (p.Asn791=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3358568	NM_032242.4(PLXNA1):c.2681A>T (p.Glu894Val)	PLXNA1 (E894V)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3358504	NM_032242.4(PLXNA1):c.2995C>T (p.Arg999Trp)	LOC129937476, PLXNA1 (R999W)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3358473	NM_032242.4(PLXNA1):c.3048C>T (p.Pro1016=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3358461	NM_032242.4(PLXNA1):c.585C>T (p.Ser195=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3358405	NM_032242.4(PLXNA1):c.2082C>T (p.Ala694=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3358403	NM_032242.4(PLXNA1):c.5645G>A (p.Arg1882Gln)	PLXNA1 (R1882Q)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3358387	NM_032242.4(PLXNA1):c.3539C>T (p.Ala1180Val)	PLXNA1 (A1180V)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3358368	NM_032242.4(PLXNA1):c.3201G>T (p.Thr1067=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GUncertain significance
Select item 3358315	NM_032242.4(PLXNA1):c.2604+4G>T	PLXNA1	Single nucleotide variant (intron variant)	PLXNA1-related disorder	GLikely benign
Select item 3358216	NM_032242.4(PLXNA1):c.2429C>T (p.Pro810Leu)	PLXNA1 (P810L)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3358153	NM_032242.4(PLXNA1):c.3008_3010del (p.Phe1003del)	LOC129937476, PLXNA1 (F1003del)	Deletion (inframe_deletion)	PLXNA1-related disorder	GUncertain significance
Select item 3358128	NM_032242.4(PLXNA1):c.4948G>A (p.Gly1650Ser)	PLXNA1 (G1650S)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3358119	NM_032242.4(PLXNA1):c.3313C>T (p.Arg1105Cys)	PLXNA1 (R1105C)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3358106	NM_032242.4(PLXNA1):c.5172G>T (p.Glu1724Asp)	PLXNA1 (E1724D)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3358081	NM_032242.4(PLXNA1):c.3387C>T (p.Val1129=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3358068	NM_032242.4(PLXNA1):c.1474C>T (p.Leu492Phe)	PLXNA1 (L492F)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3358010	NM_032242.4(PLXNA1):c.3909G>A (p.Leu1303=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3358002	NM_032242.4(PLXNA1):c.3182+9C>T	PLXNA1	Single nucleotide variant (intron variant)	PLXNA1-related disorder	GLikely benign
Select item 3357975	NM_032242.4(PLXNA1):c.836C>T (p.Thr279Met)	PLXNA1 (T279M)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3357955	NM_032242.4(PLXNA1):c.5061+7C>T	PLXNA1	Single nucleotide variant (intron variant)	PLXNA1-related disorder	GLikely benign
Select item 3357950	NM_032242.4(PLXNA1):c.759G>A (p.Glu253=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3357926	NM_032242.4(PLXNA1):c.4918A>G (p.Thr1640Ala)	PLXNA1 (T1640A)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3357890	NM_032242.4(PLXNA1):c.3592A>G (p.Thr1198Ala)	PLXNA1 (T1198A)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3357820	NM_032242.4(PLXNA1):c.1764C>T (p.Asn588=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3357769	NM_032242.4(PLXNA1):c.3015-7C>T	PLXNA1	Single nucleotide variant (intron variant)	PLXNA1-related disorder	GLikely benign
Select item 3357758	NM_032242.4(PLXNA1):c.3665G>A (p.Arg1222Gln)	PLXNA1 (R1222Q)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3357723	NM_032242.4(PLXNA1):c.2256G>A (p.Pro752=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3357649	NM_032242.4(PLXNA1):c.83C>T (p.Ala28Val)	PLXNA1 (A28V)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3357623	NM_032242.4(PLXNA1):c.5461G>A (p.Ala1821Thr)	PLXNA1 (A1821T)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3357576	NM_032242.4(PLXNA1):c.4869C>T (p.Tyr1623=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3357502	NM_032242.4(PLXNA1):c.1440C>T (p.Ala480=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3357482	NM_032242.4(PLXNA1):c.3570G>A (p.Val1190=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3357479	NM_032242.4(PLXNA1):c.3091A>G (p.Asn1031Asp)	PLXNA1 (N1031D)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3357476	NM_032242.4(PLXNA1):c.1892G>A (p.Gly631Asp)	PLXNA1 (G631D)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3357400	NM_032242.4(PLXNA1):c.3276+5G>A	PLXNA1	Single nucleotide variant (intron variant)	PLXNA1-related disorder	GUncertain significance
Select item 3357361	NM_032242.4(PLXNA1):c.*5C>T	PLXNA1	Single nucleotide variant (3 prime UTR variant)	PLXNA1-related disorder	GLikely benign
Select item 3357271	NM_032242.4(PLXNA1):c.871A>G (p.Lys291Glu)	PLXNA1 (K291E)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3357262	NM_032242.4(PLXNA1):c.1398C>T (p.Asn466=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3357248	NM_032242.4(PLXNA1):c.4062G>A (p.Ser1354=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3357205	NM_032242.4(PLXNA1):c.4164T>C (p.Asn1388=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3357094	NM_032242.4(PLXNA1):c.3136G>A (p.Glu1046Lys)	PLXNA1 (E1046K)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3357067	NM_032242.4(PLXNA1):c.4831T>G (p.Ser1611Ala)	PLXNA1 (S1611A)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3356961	NM_032242.4(PLXNA1):c.1351G>A (p.Gly451Ser)	PLXNA1 (G451S)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3356927	NM_032242.4(PLXNA1):c.300C>T (p.Ser100=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3356907	NM_032242.4(PLXNA1):c.2818T>C (p.Cys940Arg)	PLXNA1 (C940R)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3356880	NM_032242.4(PLXNA1):c.4510-7C>T	PLXNA1	Single nucleotide variant (intron variant)	PLXNA1-related disorder	GLikely benign
Select item 3356764	NM_032242.4(PLXNA1):c.2269G>A (p.Ala757Thr)	PLXNA1 (A757T)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3356758	NM_032242.4(PLXNA1):c.3703G>A (p.Val1235Met)	PLXNA1 (V1235M)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3356729	NM_032242.4(PLXNA1):c.2874C>T (p.Phe958=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3356727	NM_032242.4(PLXNA1):c.744C>T (p.Tyr248=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3356714	NM_032242.4(PLXNA1):c.3792C>G (p.Leu1264=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3356662	NM_032242.4(PLXNA1):c.1317C>T (p.Ala439=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3356659	NM_032242.4(PLXNA1):c.5519G>A (p.Arg1840His)	PLXNA1 (R1840H)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3356651	NM_032242.4(PLXNA1):c.1038G>A (p.Lys346=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3356606	NM_032242.4(PLXNA1):c.4443G>A (p.Thr1481=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GUncertain significance
Select item 3356580	NM_032242.4(PLXNA1):c.3862C>T (p.Leu1288=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3356571	NM_032242.4(PLXNA1):c.3630G>A (p.Ala1210=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3356539	NM_032242.4(PLXNA1):c.5409C>T (p.Ala1803=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3356533	NM_032242.4(PLXNA1):c.1319A>G (p.Tyr440Cys)	PLXNA1 (Y440C)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3356431	NM_032242.4(PLXNA1):c.4071G>T (p.Leu1357=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3356251	NM_032242.4(PLXNA1):c.2262T>G (p.Arg754=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3356175	NM_032242.4(PLXNA1):c.4170C>G (p.Ala1390=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3356152	NM_032242.4(PLXNA1):c.3365G>A (p.Arg1122Gln)	PLXNA1 (R1122Q)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3356043	NM_032242.4(PLXNA1):c.512G>T (p.Gly171Val)	PLXNA1 (G171V)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3356028	NM_032242.4(PLXNA1):c.4431T>A (p.Ile1477=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3355838	NM_032242.4(PLXNA1):c.2939G>T (p.Gly980Val)	LOC129937476, PLXNA1 (G980V)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3355833	NM_032242.4(PLXNA1):c.2356C>T (p.Leu786=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3355785	NM_032242.4(PLXNA1):c.2217G>A (p.Gln739=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3355770	NM_032242.4(PLXNA1):c.4899C>T (p.Pro1633=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3355742	NM_032242.4(PLXNA1):c.4653C>T (p.Ala1551=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3355724	NM_032242.4(PLXNA1):c.4278C>G (p.Pro1426=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3355706	NM_032242.4(PLXNA1):c.115C>G (p.Pro39Ala)	PLXNA1 (P39A)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3355692	NM_032242.4(PLXNA1):c.2609C>G (p.Ser870Cys)	PLXNA1 (S870C)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3355688	NM_032242.4(PLXNA1):c.2560G>A (p.Ala854Thr)	PLXNA1 (A854T)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3355667	NM_032242.4(PLXNA1):c.2113-6C>G	PLXNA1	Single nucleotide variant (intron variant)	PLXNA1-related disorder	GLikely benign
Select item 3355661	NM_032242.4(PLXNA1):c.2410+10C>T	PLXNA1	Single nucleotide variant (intron variant)	PLXNA1-related disorder	GLikely benign
Select item 3355650	NM_032242.4(PLXNA1):c.768C>T (p.Val256=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3355649	NM_032242.4(PLXNA1):c.1903C>T (p.Gln635Ter)	PLXNA1 (Q635*)	Single nucleotide variant (nonsense)	PLXNA1-related disorder	GUncertain significance
Select item 3355637	NM_032242.4(PLXNA1):c.2118C>T (p.Cys706=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3355626	NM_032242.4(PLXNA1):c.2772C>T (p.Ile924=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3355575	NM_032242.4(PLXNA1):c.1490A>G (p.Gln497Arg)	PLXNA1 (Q497R)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3355411	NM_032242.4(PLXNA1):c.5316C>T (p.Cys1772=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3355397	NM_032242.4(PLXNA1):c.2580C>T (p.Arg860=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3355385	NM_032242.4(PLXNA1):c.3183C>T (p.Ser1061=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3355314	NM_032242.4(PLXNA1):c.2312C>T (p.Ser771Leu)	PLXNA1 (S771L)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3355255	NM_032242.4(PLXNA1):c.1997C>A (p.Ser666Tyr)	PLXNA1 (S666Y)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3355197	NM_032242.4(PLXNA1):c.5578A>G (p.Thr1860Ala)	PLXNA1 (T1860A)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3355188	NM_032242.4(PLXNA1):c.4074C>T (p.Phe1358=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3355074	NM_032242.4(PLXNA1):c.2178C>A (p.Thr726=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3355062	NM_032242.4(PLXNA1):c.1408C>T (p.Arg470Trp)	PLXNA1 (R470W)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3355019	NM_032242.4(PLXNA1):c.5196C>T (p.His1732=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3354976	NM_032242.4(PLXNA1):c.4815G>A (p.Thr1605=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign
Select item 3354958	NM_032242.4(PLXNA1):c.4616C>G (p.Ala1539Gly)	PLXNA1 (A1539G)	Single nucleotide variant (missense variant)	PLXNA1-related disorder	GUncertain significance
Select item 3354927	NM_032242.4(PLXNA1):c.2868C>T (p.Phe956=)	PLXNA1	Single nucleotide variant (synonymous variant)	PLXNA1-related disorder	GLikely benign

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