WDR4[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3332823	NM_018669.6(WDR4):c.1226C>T (p.Thr409Met)	WDR4 (T409M +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2075990	NM_018669.6(WDR4):c.1223C>T (p.Ala408Val)	WDR4 (A408V +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 1357469	NM_018669.6(WDR4):c.1219G>C (p.Glu407Gln)	WDR4 (E261Q +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2054809	NM_018669.6(WDR4):c.1218G>A (p.Gly406=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1975482	NM_018669.6(WDR4):c.1215G>A (p.Pro405=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2490036	NM_018669.6(WDR4):c.1213C>A (p.Pro405Thr)	WDR4 (P405T +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1919496	NM_018669.6(WDR4):c.1202A>G (p.Lys401Arg)	WDR4 (K255R +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1482224	NM_018669.6(WDR4):c.1195C>A (p.His399Asn)	WDR4 (H398N +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2402184	NM_018669.6(WDR4):c.1191C>A (p.Asp397Glu)	WDR4 (D251E +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2831777	NM_018669.6(WDR4):c.1190A>G (p.Asp397Gly)	WDR4 (D397G +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2202110	NM_018669.6(WDR4):c.1189G>A (p.Asp397Asn)	WDR4 (D251N +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1972137	NM_018669.6(WDR4):c.1189G>T (p.Asp397Tyr)	WDR4 (D396Y +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2911701	NM_018669.6(WDR4):c.1188C>G (p.Pro396=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2413653	NM_018669.6(WDR4):c.1188C>T (p.Pro396=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2079639	NM_018669.6(WDR4):c.1183G>A (p.Gly395Arg)	WDR4 (G394R +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2856432	NM_018669.6(WDR4):c.1179G>C (p.Pro393=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1441087	NM_018669.6(WDR4):c.1178C>T (p.Pro393Leu)	WDR4 (P247L +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1234975	NM_018669.6(WDR4):c.1169G>A (p.Arg390Gln)	WDR4 (R244Q +2 more)	Single nucleotide variant (missense variant +1 more)	Galloway-Mowat syndrome 6 +2 more	GBenign
Select item 2144900	NM_018669.6(WDR4):c.1168C>T (p.Arg390Trp)	WDR4 (R244W +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2176666	NM_018669.6(WDR4):c.1165C>T (p.Arg389Cys)	WDR4 (R388C +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2367585	NM_018669.6(WDR4):c.1163G>A (p.Arg388Gln)	WDR4 (R242Q +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2130364	NM_018669.6(WDR4):c.1159C>T (p.Gln387Ter)	WDR4 (Q386* +2 more)	Single nucleotide variant (nonsense +1 more)	not provided	GPathogenic
Select item 2070451	NM_018669.6(WDR4):c.1156A>C (p.Lys386Gln)	WDR4 (K385Q +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2410573	NM_018669.6(WDR4):c.1150G>A (p.Glu384Lys)	WDR4 (E383K +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2059339	NM_018669.6(WDR4):c.1149A>G (p.Leu383=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2410572	NM_018669.6(WDR4):c.1148T>C (p.Leu383Pro)	WDR4 (L237P +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2707214	NM_018669.6(WDR4):c.1137G>A (p.Leu379=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3332828	NM_018669.6(WDR4):c.1134A>C (p.Arg378Ser)	WDR4 (R378S +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1510448	NM_018669.6(WDR4):c.1131G>C (p.Glu377Asp)	WDR4 (E231D +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 3190029	NM_018669.6(WDR4):c.1129G>A (p.Glu377Lys)	WDR4 (E376K +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1566816	NM_018669.6(WDR4):c.1122G>A (p.Lys374=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2607983	NM_018669.6(WDR4):c.1120A>C (p.Lys374Gln)	WDR4 (K373Q +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2119481	NM_018669.6(WDR4):c.1119G>C (p.Lys373Asn)	WDR4 (K372N +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2331446	NM_018669.6(WDR4):c.1114C>G (p.Leu372Val)	WDR4 (L371V +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3044986	NM_018669.6(WDR4):c.1107C>A (p.Thr369=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	WDR4-related disorder	GLikely benign
Select item 2138390	NM_018669.6(WDR4):c.1106C>T (p.Thr369Ile)	WDR4 (T223I +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1977210	NM_018669.6(WDR4):c.1101C>T (p.Asn367=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3047870	NM_018669.6(WDR4):c.1095C>T (p.Phe365=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	WDR4-related disorder	GLikely benign
Select item 2183383	NM_018669.6(WDR4):c.1091C>A (p.Thr364Lys)	WDR4 (T364K +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1288640	NM_018669.6(WDR4):c.1089C>T (p.Ala363=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 3040371	NM_018669.6(WDR4):c.1071C>A (p.Phe357Leu)	WDR4 (F211L +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2652715	NM_018669.6(WDR4):c.1071C>T (p.Phe357=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1577782	NM_018669.6(WDR4):c.1056C>T (p.Gly352=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3190028	NM_018669.6(WDR4):c.1054G>C (p.Gly352Arg)	WDR4 (G351R +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2005789	NM_018669.6(WDR4):c.1054G>T (p.Gly352Cys)	WDR4 (G351C +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1927972	NM_018669.6(WDR4):c.1053C>T (p.Ala351=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1977909	NM_018669.6(WDR4):c.1047C>T (p.Gly349=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2044965	NM_018669.6(WDR4):c.1046-1G>A	WDR4	Single nucleotide variant (splice acceptor variant)	not provided	GUncertain significance
Select item 2255312	NM_018669.6(WDR4):c.1046-3C>T	WDR4	Single nucleotide variant (intron variant)	Inborn genetic diseases	GUncertain significance
Select item 1979313	NM_018669.6(WDR4):c.1046-4A>G	WDR4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2762884	NM_018669.6(WDR4):c.1046-16T>C	WDR4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2051888	NM_018669.6(WDR4):c.1046-18C>T	WDR4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1257157	NM_018669.6(WDR4):c.1046-50G>C	WDR4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1276144	NM_018669.6(WDR4):c.1046-149C>T	WDR4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1229045	NM_018669.6(WDR4):c.1045+38C>T	WDR4	Single nucleotide variant (intron variant)	Galloway-Mowat syndrome 6 +2 more	GBenign
Select item 2864735	NM_018669.6(WDR4):c.1045+11G>A	WDR4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2047233	NM_018669.6(WDR4):c.1045+10C>T	WDR4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2177762	NM_018669.6(WDR4):c.1045+8C>T	WDR4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 726110	NM_018669.6(WDR4):c.1036A>G (p.Met346Val)	WDR4 (M345V +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2076780	NM_018669.6(WDR4):c.1021C>T (p.Arg341Cys)	WDR4 (R340C +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 2376377	NM_018669.6(WDR4):c.994G>A (p.Val332Met)	WDR4 (V332M +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2033616	NM_018669.6(WDR4):c.976T>A (p.Ser326Thr)	WDR4 (S325T +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 710985	NM_018669.6(WDR4):c.976-9C>T	WDR4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1276702	NM_018669.6(WDR4):c.976-174T>C	WDR4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2006420	NM_018669.6(WDR4):c.975+13A>G	WDR4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1991327	NM_018669.6(WDR4):c.975+9C>T	WDR4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1390003	NM_018669.6(WDR4):c.975+3G>A	WDR4	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1601679	NM_018669.6(WDR4):c.963C>T (p.Gly321=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1435258	NM_018669.6(WDR4):c.956C>G (p.Pro319Arg)	WDR4 (P319R +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 438742	NM_018669.6(WDR4):c.940dup (p.Leu314fs)	WDR4 (L168fs +2 more)	Duplication (frameshift variant +1 more)	Galloway-Mowat syndrome 6	GPathogenic
Select item 2788729	NM_018669.6(WDR4):c.930G>A (p.Gln310=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 619602	NM_018669.6(WDR4):c.911_927dup (p.Gln310fs)	WDR4 (Q164fs +2 more)	Duplication (frameshift variant +1 more)	not provided	GPathogenic
Select item 1247972	NM_018669.6(WDR4):c.891C>T (p.Phe297=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2867808	NM_018669.6(WDR4):c.882C>T (p.Asp294=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2867347	NM_018669.6(WDR4):c.876G>C (p.Val292=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2727439	NM_018669.6(WDR4):c.870C>T (p.His290=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2152965	NM_018669.6(WDR4):c.866A>G (p.Gln289Arg)	WDR4 (Q288R +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 1571314	NM_018669.6(WDR4):c.861G>A (p.Ala287=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign/Likely benign
Select item 2059863	NM_018669.6(WDR4):c.841G>T (p.Val281Leu)	WDR4 (V280L +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2065828	NM_018669.6(WDR4):c.837G>A (p.Gln279=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2847850	NM_018669.6(WDR4):c.825C>T (p.Ala275=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2194058	NM_018669.6(WDR4):c.823G>A (p.Ala275Thr)	WDR4 (A275T +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 1981192	NM_018669.6(WDR4):c.822C>T (p.Asp274=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2052448	NM_018669.6(WDR4):c.821A>T (p.Asp274Val)	WDR4 (D128V +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2396240	NM_018669.6(WDR4):c.799G>A (p.Val267Met)	WDR4 (V267M +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2063755	NM_018669.6(WDR4):c.798T>C (p.Pro266=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1221407	NM_018669.6(WDR4):c.796C>T (p.Pro266Ser)	WDR4 (P120S +2 more)	Single nucleotide variant (missense variant +1 more)	Microcephaly, growth deficiency, seizures, and brain malformations +2 more	GBenign
Select item 2147004	NM_018669.6(WDR4):c.792-4C>T	WDR4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2070398	NM_018669.6(WDR4):c.792-9C>T	WDR4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1225241	NM_018669.6(WDR4):c.792-145A>T	WDR4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1283721	NM_018669.6(WDR4):c.791+30C>T	WDR4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1974715	NM_018669.6(WDR4):c.791+13G>A	WDR4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1578990	NM_018669.6(WDR4):c.791+12C>T	WDR4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2873576	NM_018669.6(WDR4):c.791+11G>A	WDR4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2751459	NM_018669.6(WDR4):c.791+9C>T	WDR4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2067868	NM_018669.6(WDR4):c.791+4A>G	WDR4	Single nucleotide variant (intron variant)	not provided +1 more	GUncertain significance
Select item 2541661	NM_018669.6(WDR4):c.790G>A (p.Gly264Ser)	WDR4 (G118S +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2062624	NM_018669.6(WDR4):c.789C>T (p.Asp263=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3332829	NM_018669.6(WDR4):c.787G>A (p.Asp263Asn)	WDR4 (D263N +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2297972	NM_018669.6(WDR4):c.779_786del (p.Leu260fs)	WDR4 (L259fs +2 more)	Deletion (frameshift variant +1 more)	Inborn genetic diseases	GPathogenic

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