LZTR1[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2433581	NM_006767.4(LZTR1):c.-975G>A	LZTR1	Single nucleotide variant	not provided	GUncertain significance
Select item 561839	NM_006767.3(LZTR1):c.-299G>A	LZTR1	Single nucleotide variant	not provided	GBenign
Select item 561399	NM_006767.3(LZTR1):c.-160G>C	LZTR1	Single nucleotide variant	not provided	GBenign
Select item 561400	NM_006767.3(LZTR1):c.-112A>T	LZTR1	Single nucleotide variant	not provided	GBenign
Select item 549752	NM_006767.4(LZTR1):c.-38T>A	LZTR1	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome +5 more	GConflicting classifications of pathogenicity
Select item 389662	NM_006767.4(LZTR1):c.-11G>A	LZTR1	Single nucleotide variant (5 prime UTR variant)	not provided +1 more	GBenign/Likely benign
Select item 2175404	NM_006767.4(LZTR1):c.126G>A (p.Thr42=)	LZTR1	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 1770791	NM_006767.4(LZTR1):c.135C>T (p.Phe45=)	LZTR1	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 1770783	NM_006767.4(LZTR1):c.135C>G (p.Phe45Leu)	LZTR1 (F45L)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 1770780	NM_006767.4(LZTR1):c.135C>A (p.Phe45Leu)	LZTR1 (F45L)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 1485823	NM_006767.4(LZTR1):c.136G>A (p.Gly46Arg)	LZTR1 (G46R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 1373275	NM_006767.4(LZTR1):c.136G>T (p.Gly46Trp)	LZTR1 (G46W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1076017	NM_006767.4(LZTR1):c.138del (p.Phe48fs)	LZTR1 (F48fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 1095011	NM_006767.4(LZTR1):c.138G>A (p.Gly46=)	LZTR1	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +3 more	GLikely benign
Select item 1771724	NM_006767.4(LZTR1):c.139C>T (p.Pro47Ser)	LZTR1 (P47S)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 1771717	NM_006767.4(LZTR1):c.139C>A (p.Pro47Thr)	LZTR1 (P47T)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1771986	NM_006767.4(LZTR1):c.140C>T (p.Pro47Leu)	LZTR1 (P47L)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 1432766	NM_006767.4(LZTR1):c.140C>A (p.Pro47His)	LZTR1 (P47H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3238081	NM_006767.4(LZTR1):c.142T>G (p.Phe48Val)	LZTR1 (F48V)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 1772888	NM_006767.4(LZTR1):c.144C>T (p.Phe48=)	LZTR1	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 1772885	NM_006767.4(LZTR1):c.144C>G (p.Phe48Leu)	LZTR1 (F48L)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 3238083	NM_006767.4(LZTR1):c.145G>T (p.Glu49Ter)	LZTR1 (E49*)	Single nucleotide variant (nonsense)	Cardiovascular phenotype +1 more	GPathogenic
Select item 2111726	NM_006767.4(LZTR1):c.148del (p.Thr50fs)	LZTR1 (T50fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 1773316	NM_006767.4(LZTR1):c.146A>C (p.Glu49Ala)	LZTR1 (E49A)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 1773517	NM_006767.4(LZTR1):c.147A>G (p.Glu49=)	LZTR1	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 3238090	NM_006767.4(LZTR1):c.150A>G (p.Thr50=)	LZTR1	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 1774152	NM_006767.4(LZTR1):c.150A>T (p.Thr50=)	LZTR1	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 524146	NM_006767.4(LZTR1):c.150_151del (p.Val51fs)	LZTR1 (V51fs)	Deletion (frameshift variant)	not provided	GPathogenic/Likely pathogenic
Select item 1774822	NM_006767.4(LZTR1):c.153G>T (p.Val51=)	LZTR1	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 1775016	NM_006767.4(LZTR1):c.154C>T (p.His52Tyr)	LZTR1 (H52Y)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 1367701	NM_006767.4(LZTR1):c.154_155delinsAT (p.His52Ile)	LZTR1 (H52I)	Indel (missense variant)	not provided	GUncertain significance
Select item 3238098	NM_006767.4(LZTR1):c.155A>G (p.His52Arg)	LZTR1 (H52R)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 1408470	NM_006767.4(LZTR1):c.157C>T (p.Arg53Cys)	LZTR1 (R53C)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 3252123	NM_006767.4(LZTR1):c.160_171del (p.Trp54_Leu57del)	LZTR1	Deletion (inframe_deletion)	not provided	GUncertain significance
Select item 3238108	NM_006767.4(LZTR1):c.159C>T (p.Arg53=)	LZTR1	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 2445734	NM_006767.4(LZTR1):c.160T>G (p.Trp54Gly)	LZTR1 (W54G)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 1776372	NM_006767.4(LZTR1):c.160T>C (p.Trp54Arg)	LZTR1 (W54R)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +2 more	GUncertain significance
Select item 2857702	NM_006767.4(LZTR1):c.162GCG[1] (p.Arg56del)	LZTR1 (R56del)	Microsatellite (inframe_deletion)	not provided	GUncertain significance
Select item 1777238	NM_006767.4(LZTR1):c.165_181dup (p.Asp61fs)	LZTR1 (D61fs)	Duplication (frameshift variant)	Cardiovascular phenotype +1 more	GPathogenic
Select item 1776577	NM_006767.4(LZTR1):c.161G>A (p.Trp54Ter)	LZTR1 (W54*)	Single nucleotide variant (nonsense)	Cardiovascular phenotype +1 more	GPathogenic
Select item 2960734	NM_006767.4(LZTR1):c.162G>A (p.Trp54Ter)	LZTR1 (W54*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 1710263	NM_006767.4(LZTR1):c.163C>T (p.Arg55Trp)	LZTR1 (R55W)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 985816	NM_006767.4(LZTR1):c.163C>G (p.Arg55Gly)	LZTR1 (R55G)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1777450	NM_006767.4(LZTR1):c.165G>A (p.Arg55=)	LZTR1	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 1777873	NM_006767.4(LZTR1):c.167G>A (p.Arg56His)	LZTR1 (R56H)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 2443451	NM_006767.4(LZTR1):c.170T>G (p.Leu57Arg)	LZTR1 (L57R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3241863	NM_006767.4(LZTR1):c.173C>T (p.Pro58Leu)	LZTR1 (P58L)	Single nucleotide variant (missense variant)	Schwannomatosis 2	GUncertain significance
Select item 429914	NM_006767.4(LZTR1):c.173C>G (p.Pro58Arg)	LZTR1 (P58R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3238127	NM_006767.4(LZTR1):c.176C>T (p.Pro59Leu)	LZTR1 (P59L)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 1779946	NM_006767.4(LZTR1):c.177C>T (p.Pro59=)	LZTR1	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +2 more	GLikely benign
Select item 2696874	NM_006767.4(LZTR1):c.178T>C (p.Cys60Arg)	LZTR1 (C60R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2833568	NM_006767.4(LZTR1):c.179G>C (p.Cys60Ser)	LZTR1 (C60S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3238136	NM_006767.4(LZTR1):c.180C>G (p.Cys60Trp)	LZTR1 (C60W)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 1661677	NM_006767.4(LZTR1):c.180C>T (p.Cys60=)	LZTR1	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 1071200	NM_006767.4(LZTR1):c.180C>A (p.Cys60Ter)	LZTR1 (C60*)	Single nucleotide variant (nonsense)	Hereditary cancer-predisposing syndrome +2 more	GPathogenic
Select item 1781117	NM_006767.4(LZTR1):c.183C>T (p.Asp61=)	LZTR1	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 1709295	NM_006767.4(LZTR1):c.184del (p.Glu62fs)	LZTR1 (E62fs)	Deletion (frameshift variant)	Schwannomatosis 2	GLikely pathogenic
Select item 835137	NM_006767.4(LZTR1):c.184G>A (p.Glu62Lys)	LZTR1 (E62K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3003995	NM_006767.4(LZTR1):c.185A>T (p.Glu62Val)	LZTR1 (E62V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2446097	NM_006767.4(LZTR1):c.187T>C (p.Phe63Leu)	LZTR1 (F63L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2191583	NM_006767.4(LZTR1):c.188T>G (p.Phe63Cys)	LZTR1 (F63C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1782481	NM_006767.4(LZTR1):c.190G>A (p.Val64Met)	LZTR1 (V64M)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 1782847	NM_006767.4(LZTR1):c.192G>A (p.Val64=)	LZTR1	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 1782871	NM_006767.4(LZTR1):c.193_195delinsA (p.Gly65fs)	LZTR1 (G65fs)	Indel (frameshift variant)	Cardiovascular phenotype +1 more	GPathogenic
Select item 1783197	NM_006767.4(LZTR1):c.194G>A (p.Gly65Asp)	LZTR1 (G65D)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 1783407	NM_006767.4(LZTR1):c.195T>A (p.Gly65=)	LZTR1	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 1783586	NM_006767.4(LZTR1):c.196G>A (p.Ala66Thr)	LZTR1 (A66T)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 3238186	NM_006767.4(LZTR1):c.199del (p.Arg67fs)	LZTR1 (R67fs)	Deletion (frameshift variant)	Cardiovascular phenotype +1 more	GPathogenic
Select item 3018834	NM_006767.4(LZTR1):c.199C>T (p.Arg67Trp)	LZTR1 (R67W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2447723	NM_006767.4(LZTR1):c.199C>G (p.Arg67Gly)	LZTR1 (R67G)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 2022453	NM_006767.4(LZTR1):c.199C>A (p.Arg67=)	LZTR1	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 1784227	NM_006767.4(LZTR1):c.200+1dup	LZTR1	Duplication (splice donor variant)	Schwannomatosis 2 +3 more	GPathogenic/Likely pathogenic
Select item 2696442	NM_006767.4(LZTR1):c.200G>T (p.Arg67Leu)	LZTR1 (R67L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1784387	NM_006767.4(LZTR1):c.200G>C (p.Arg67Pro)	LZTR1 (R67P)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 2413554	NM_006767.4(LZTR1):c.200+1G>T	LZTR1	Single nucleotide variant (splice donor variant)	Hereditary cancer-predisposing syndrome +2 more	GLikely pathogenic
Select item 1982526	NM_006767.4(LZTR1):c.200+1G>C	LZTR1	Single nucleotide variant (splice donor variant)	Schwannomatosis 2 +1 more	GLikely pathogenic
Select item 2441303	NM_006767.4(LZTR1):c.200+2T>C	LZTR1	Single nucleotide variant (splice donor variant)	not provided +1 more	GLikely pathogenic
Select item 1784228	NM_006767.4(LZTR1):c.200+2T>A	LZTR1	Single nucleotide variant (splice donor variant)	Cardiovascular phenotype +1 more	GLikely pathogenic
Select item 1467001	NM_006767.4(LZTR1):c.200+2T>G	LZTR1	Single nucleotide variant (splice donor variant)	not provided	GLikely pathogenic
Select item 2676386	NM_006767.4(LZTR1):c.200+3A>G	LZTR1	Single nucleotide variant (intron variant)	Schwannomatosis 2 +1 more	GUncertain significance
Select item 1463020	NM_006767.4(LZTR1):c.200+4C>T	LZTR1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1784229	NM_006767.4(LZTR1):c.200+5G>A	LZTR1	Single nucleotide variant (intron variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 2887195	NM_006767.4(LZTR1):c.200+9G>A	LZTR1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1227303	NM_006767.4(LZTR1):c.200+79G>A	LZTR1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 561673	NM_006767.4(LZTR1):c.201-172C>A	LZTR1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1246352	NM_006767.4(LZTR1):c.201-142T>A	LZTR1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 561409	NM_006767.4(LZTR1):c.201-50G>A	LZTR1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1187148	NM_006767.4(LZTR1):c.201-40A>G	LZTR1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1914606	NM_006767.4(LZTR1):c.201-15C>T	LZTR1	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 496334	NM_006767.4(LZTR1):c.201-13C>T	LZTR1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 3011080	NM_006767.4(LZTR1):c.201-12C>T	LZTR1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2973690	NM_006767.4(LZTR1):c.201-12C>G	LZTR1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2059490	NM_006767.4(LZTR1):c.201-7_201-4del	LZTR1	Microsatellite (intron variant)	not provided	GLikely benign
Select item 2627113	NM_006767.4(LZTR1):c.201-11T>G	LZTR1	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 2848257	NM_006767.4(LZTR1):c.201-10T>C	LZTR1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 496335	NM_006767.4(LZTR1):c.201-8C>T	LZTR1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 1784429	NM_006767.4(LZTR1):c.201-1G>A	LZTR1	Single nucleotide variant (splice acceptor variant)	Schwannomatosis 2 +2 more	GConflicting classifications of pathogenicity
Select item 1415999	NM_006767.4(LZTR1):c.202C>T (p.Arg68Cys)	LZTR1 (R68C)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 280158	NM_006767.4(LZTR1):c.202C>A (p.Arg68Ser)	LZTR1 (R68S)	Single nucleotide variant (missense variant)	Schwannomatosis 2 +1 more	GUncertain significance
Select item 1784884	NM_006767.4(LZTR1):c.203G>T (p.Arg68Leu)	LZTR1 (R68L)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance

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