"GeneDx"[submitter] AND "USP9X"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1230956	NM_001039591.3(USP9X):c.-158-329G>A	USP9X	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1246199	NM_001039591.3(USP9X):c.-158-287G>A	USP9X	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1289835	NM_001039591.3(USP9X):c.-158-83C>T	USP9X	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1309601	NM_001039591.3(USP9X):c.52C>G (p.Gln18Glu)	USP9X (Q18E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1254438	NM_001039591.3(USP9X):c.82dup (p.Leu28fs)	USP9X (L28fs)	Duplication (frameshift variant)	Inborn genetic diseases +1 more	GPathogenic
Select item 1312256	NM_001039591.3(USP9X):c.92A>G (p.Asn31Ser)	USP9X (N31S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1273629	NM_001039591.3(USP9X):c.96+233T>C	USP9X	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1803499	NM_001039591.3(USP9X):c.144A>C (p.Pro48=)	USP9X	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 1205264	NM_001039591.3(USP9X):c.172C>T (p.Pro58Ser)	USP9X (P58S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1704754	NM_001039591.3(USP9X):c.190G>A (p.Glu64Lys)	USP9X (E64K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2504555	NM_001039591.3(USP9X):c.209C>G (p.Thr70Ser)	USP9X (T70S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1309701	NM_001039591.3(USP9X):c.235A>G (p.Ile79Val)	USP9X (I79V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2503160	NM_001039591.3(USP9X):c.236T>A (p.Ile79Asn)	USP9X (I79N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1267105	NM_001039591.3(USP9X):c.243-173G>T	USP9X	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3367758	NM_001039591.3(USP9X):c.272A>G (p.Lys91Arg)	USP9X (K91R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1321631	NM_001039591.3(USP9X):c.304A>G (p.Ile102Val)	USP9X (I102V)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GBenign/Likely benign
Select item 1278185	NM_001039591.3(USP9X):c.323-272A>G	USP9X	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1237961	NM_001039591.3(USP9X):c.323-71T>G	USP9X	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1257818	NM_001039591.3(USP9X):c.323-40G>A	USP9X	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1303552	NM_001039591.3(USP9X):c.334A>C (p.Lys112Gln)	USP9X (K112Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 393045	NM_001039591.3(USP9X):c.367G>T (p.Gly123Trp)	USP9X (G123W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 427036	NM_001039591.3(USP9X):c.392T>A (p.Ile131Asn)	USP9X (I131N)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 1810710	NM_001039591.3(USP9X):c.397A>G (p.Thr133Ala)	USP9X (T133A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3369239	NM_001039591.3(USP9X):c.434A>C (p.His145Pro)	USP9X (H145P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1284141	NM_001039591.3(USP9X):c.435+36A>G	USP9X	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1200295	NM_001039591.3(USP9X):c.436-255G>A	USP9X	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1276767	NM_001039591.3(USP9X):c.436-237T>A	USP9X	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1202364	NM_001039591.3(USP9X):c.460C>T (p.Arg154Cys)	USP9X (R154C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1327230	NM_001039591.3(USP9X):c.511T>C (p.Leu171=)	USP9X	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 372979	NM_001039591.3(USP9X):c.517CTT[1] (p.Leu174del)	USP9X (L174del)	Microsatellite (inframe_deletion)	not provided	GPathogenic
Select item 452013	NM_001039591.3(USP9X):c.542A>T (p.His181Leu)	USP9X (H181L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1700466	NM_001039591.3(USP9X):c.547A>G (p.Lys183Glu)	USP9X (K183E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 384085	NM_001039591.3(USP9X):c.562A>G (p.Asn188Asp)	USP9X (N188D)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 1314593	NM_001039591.3(USP9X):c.565G>A (p.Gly189Ser)	USP9X (G189S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2446265	NM_001039591.3(USP9X):c.571C>T (p.Arg191Cys)	USP9X (R191C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 721988	NM_001039591.3(USP9X):c.595A>G (p.Ser199Gly)	USP9X (S199G)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1308505	NM_001039591.3(USP9X):c.626C>G (p.Ala209Gly)	USP9X (A209G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1219208	NM_001039591.3(USP9X):c.628C>T (p.Arg210Cys)	USP9X (R210C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3370835	NM_001039591.3(USP9X):c.641C>T (p.Pro214Leu)	USP9X (P214L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 391824	NM_001039591.3(USP9X):c.643C>T (p.Arg215Ter)	USP9X (R215*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 1291771	NM_001039591.3(USP9X):c.654+38A>G	USP9X	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1193660	NM_001039591.3(USP9X):c.654+98A>G	USP9X	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1259335	NM_001039591.3(USP9X):c.655-316A>C	USP9X	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1283199	NM_001039591.3(USP9X):c.655-225G>A	USP9X	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1249754	NM_001039591.3(USP9X):c.655-56C>A	USP9X	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1708869	NM_001039591.3(USP9X):c.724A>G (p.Ile242Val)	USP9X (I242V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3376092	NM_001039591.3(USP9X):c.779G>A (p.Gly260Glu)	USP9X (G260E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1307560	NM_001039591.3(USP9X):c.848C>T (p.Pro283Leu)	USP9X (P283L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1313961	NM_001039591.3(USP9X):c.883A>G (p.Lys295Glu)	USP9X (K295E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1307353	NM_001039591.3(USP9X):c.904G>A (p.Ala302Thr)	USP9X (A302T)	Single nucleotide variant (missense variant)	Intellectual disability, X-linked 99 +1 more	GUncertain significance
Select item 1810499	NM_001039591.3(USP9X):c.965C>T (p.Pro322Leu)	USP9X (P322L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3363604	NM_001039591.3(USP9X):c.991T>A (p.Leu331Ile)	USP9X (L331I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1326610	NM_001039591.3(USP9X):c.991T>C (p.Leu331=)	USP9X	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 2499260	NM_001039591.3(USP9X):c.1073T>A (p.Val358Asp)	USP9X (V358D)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 1191978	NM_001039591.3(USP9X):c.1095A>G (p.Val365=)	USP9X	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 1800610	NM_001039591.3(USP9X):c.1103A>G (p.Tyr368Cys)	USP9X (Y368C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3369037	NM_001039591.3(USP9X):c.1108C>T (p.His370Tyr)	USP9X (H370Y)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 280380	NM_001039591.3(USP9X):c.1140G>A (p.Trp380Ter)	USP9X (W380*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 1182762	NM_001039591.3(USP9X):c.1161+193A>G	USP9X	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1208243	NM_001039591.3(USP9X):c.1162-46T>C	USP9X	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3343513	NM_001039591.3(USP9X):c.1201C>T (p.Arg401Ter)	USP9X (R401*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 1678679	NM_001039591.3(USP9X):c.1202G>A (p.Arg401Gln)	USP9X (R401Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 422179	NM_001039591.3(USP9X):c.1303T>C (p.Trp435Arg)	USP9X (W435R)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 1263421	NM_001039591.3(USP9X):c.1314+148T>C	USP9X	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1204363	NM_001039591.3(USP9X):c.1314+317T>C	USP9X	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1288929	NM_001039591.3(USP9X):c.1315-285dup	USP9X	Duplication (intron variant)	not provided	GBenign
Select item 1215983	NM_001039591.3(USP9X):c.1315-286_1315-285dup	USP9X	Duplication (intron variant)	not provided	GLikely benign
Select item 1250714	NM_001039591.3(USP9X):c.1315-285_1315-284insTG	USP9X	Insertion (intron variant)	not provided	GBenign
Select item 1270521	NM_001039591.3(USP9X):c.1315-263G>T	USP9X	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 384654	NM_001039591.3(USP9X):c.1315-4A>G	USP9X	Single nucleotide variant (intron variant)	Intellectual disability, X-linked 99, syndromic, female-restricted +2 more	GPathogenic/Likely pathogenic
Select item 450123	NM_001039591.3(USP9X):c.1327G>A (p.Glu443Lys)	USP9X (E443K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 452886	NM_001039591.3(USP9X):c.1374G>A (p.Trp458Ter)	USP9X (W458*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 1241473	NM_001039591.3(USP9X):c.1419+24T>C	USP9X	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1810583	NM_001039591.3(USP9X):c.1477C>T (p.Arg493Cys)	USP9X (R493C)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 3378179	NM_001039591.3(USP9X):c.1610A>T (p.Asp537Val)	USP9X (D537V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3378150	NM_001039591.3(USP9X):c.1610A>G (p.Asp537Gly)	USP9X (D537G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1253070	NM_001039591.3(USP9X):c.1626+112C>T	USP9X	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1215402	NM_001039591.3(USP9X):c.1626+270C>T	USP9X	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1198018	NM_001039591.3(USP9X):c.1627-138C>A	USP9X	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1197383	NM_001039591.3(USP9X):c.1627-136T>C	USP9X	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1191014	NM_001039591.3(USP9X):c.1660C>G (p.Arg554Gly)	USP9X (R554G)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1310320	NM_001039591.3(USP9X):c.1678C>T (p.Arg560Cys)	USP9X (R560C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2574452	NM_001039591.3(USP9X):c.1687G>A (p.Asp563Asn)	USP9X (D563N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1800920	NM_001039591.3(USP9X):c.1748C>T (p.Ala583Val)	USP9X (A583V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1233902	NM_001039591.3(USP9X):c.1763+173del	USP9X	Deletion (intron variant)	not provided	GBenign
Select item 1289163	NM_001039591.3(USP9X):c.1764-275G>A	USP9X	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1248190	NM_001039591.3(USP9X):c.1764-166del	USP9X	Deletion (intron variant)	not provided	GBenign
Select item 1258587	NM_001039591.3(USP9X):c.1764-99G>T	USP9X	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1227131	NM_001039591.3(USP9X):c.1764-50A>G	USP9X	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1304170	NM_001039591.3(USP9X):c.1764-8C>A	USP9X	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2412920	NM_001039591.3(USP9X):c.1790T>A (p.Phe597Tyr)	USP9X (F597Y +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1338821	NM_001039591.3(USP9X):c.1812_1815del (p.Gln605fs)	USP9X (Q605fs)	Microsatellite (frameshift variant)	not provided +1 more	GPathogenic
Select item 3252189	NM_001039591.3(USP9X):c.1813C>G (p.Gln605Glu)	USP9X (Q605E +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 562221	NM_001039591.3(USP9X):c.1877G>A (p.Ser626Asn)	USP9X (S626N)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1678805	NM_001039591.3(USP9X):c.1881G>C (p.Met627Ile)	USP9X (M627I)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1698008	NM_001039591.3(USP9X):c.1892C>T (p.Ala631Val)	USP9X (A631V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1326161	NM_001039591.3(USP9X):c.1897G>A (p.Asp633Asn)	USP9X (D633N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1242950	NM_001039591.3(USP9X):c.1897+153_1897+154del	USP9X	Deletion (intron variant)	not provided	GBenign
Select item 1182475	NM_001039591.3(USP9X):c.1897+280A>C	USP9X	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1250246	NM_001039591.3(USP9X):c.1897+299T>C	USP9X	Single nucleotide variant (intron variant)	not provided	GBenign

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