WDR38[gene] and "single gene"[properties] - ClinVar

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Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2410638	NM_001045476.3(WDR38):c.74A>G (p.Asn25Ser)	WDR38 (N25S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2494112	NM_001045476.3(WDR38):c.204C>A (p.Phe68Leu)	WDR38 (F68L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3332818	NM_001045476.3(WDR38):c.238A>G (p.Ser80Gly)	WDR38 (S69G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2341496	NM_001045476.3(WDR38):c.284C>T (p.Ala95Val)	WDR38 (A84V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190018	NM_001045476.3(WDR38):c.315A>T (p.Gln105His)	WDR38 (Q105H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190019	NM_001045476.3(WDR38):c.361G>A (p.Ala121Thr)	WDR38 (A121T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509211	NM_001045476.3(WDR38):c.382C>T (p.Arg128Trp)	WDR38 (R117W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469827	NM_001045476.3(WDR38):c.410G>A (p.Gly137Asp)	WDR38 (G137D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523512	NM_001045476.3(WDR38):c.422G>A (p.Arg141His)	WDR38 (R141H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190020	NM_001045476.3(WDR38):c.436C>T (p.His146Tyr)	WDR38 (H135Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208222	NM_001045476.3(WDR38):c.439C>T (p.Arg147Cys)	WDR38 (R98C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332817	NM_001045476.3(WDR38):c.440G>A (p.Arg147His)	WDR38 (R98H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332820	NM_001045476.3(WDR38):c.455G>A (p.Ser152Asn)	WDR38 (S103N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332821	NM_001045476.3(WDR38):c.460G>A (p.Asp154Asn)	WDR38 (D105N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455801	NM_001045476.3(WDR38):c.560C>T (p.Ala187Val)	WDR38 (A138V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332819	NM_001045476.3(WDR38):c.588C>G (p.Ser196Arg)	WDR38 (S196R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190021	NM_001045476.3(WDR38):c.716T>C (p.Ile239Thr)	WDR38 (I239T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332822	NM_001045476.3(WDR38):c.734A>G (p.Glu245Gly)	WDR38 (E245G +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3190022	NM_001045476.3(WDR38):c.758A>G (p.Tyr253Cys)	WDR38 (Y242C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190023	NM_001045476.3(WDR38):c.763C>T (p.Arg255Cys)	WDR38 (R206C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190024	NM_001045476.3(WDR38):c.784T>C (p.Cys262Arg)	WDR38 (C251R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190025	NM_001045476.3(WDR38):c.806A>C (p.Glu269Ala)	WDR38 (E269A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293839	NM_001045476.3(WDR38):c.889C>A (p.Gln297Lys)	WDR38 (Q297K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190026	NM_001045476.3(WDR38):c.898C>T (p.Arg300Cys)	WDR38 (R252C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401714	NM_001045476.3(WDR38):c.910C>T (p.Arg304Cys)	WDR38 (R256C +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2570528	NM_001045476.3(WDR38):c.911G>A (p.Arg304His)	WDR38 (R304H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190027	NM_001045476.3(WDR38):c.919A>C (p.Lys307Gln)	WDR38 (K307Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 27