"WDR11-related condition"[Disease/phenotype] AND "PreventionGenetics, - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2635621	NM_018117.12(WDR11):c.8C>T (p.Pro3Leu)	WDR11 (P3L)	Single nucleotide variant (missense variant)	WDR11-related condition	GUncertain significance
Select item 704337	NM_018117.12(WDR11):c.288C>T (p.Ile96=)	WDR11	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2631485	NM_018117.12(WDR11):c.352+1G>A	WDR11	Single nucleotide variant (splice donor variant)	WDR11-related condition	GLikely pathogenic
Select item 695236	NM_018117.12(WDR11):c.1066G>A (p.Val356Ile)	WDR11 (V356I)	Single nucleotide variant (missense variant)	WDR11-related condition +1 more	GBenign/Likely benign
Select item 703311	NM_018117.12(WDR11):c.1113C>T (p.Ala371=)	WDR11	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 2982464	NM_018117.12(WDR11):c.1497G>A (p.Val499=)	WDR11	Single nucleotide variant (synonymous variant)	WDR11-related condition +1 more	GLikely benign
Select item 695275	NM_018117.12(WDR11):c.1944G>A (p.Glu648=)	WDR11	Single nucleotide variant (synonymous variant)	WDR11-related condition +1 more	GBenign
Select item 3056425	NM_018117.12(WDR11):c.2046C>T (p.Thr682=)	WDR11	Single nucleotide variant (synonymous variant)	WDR11-related condition	GLikely benign
Select item 2851895	NM_018117.12(WDR11):c.2867G>A (p.Arg956Gln)	WDR11 (R956Q)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 695194	NM_018117.12(WDR11):c.2962G>A (p.Glu988Lys)	WDR11 (E988K)	Single nucleotide variant (missense variant)	WDR11-related condition +1 more	GBenign/Likely benign
Select item 3032312	NM_018117.12(WDR11):c.3258C>T (p.Tyr1086=)	WDR11	Single nucleotide variant (synonymous variant)	WDR11-related condition	GLikely benign
Select item 2630475	NM_018117.12(WDR11):c.3331C>T (p.Arg1111Trp)	WDR11 (R1111W)	Single nucleotide variant (missense variant)	WDR11-related condition	GUncertain significance
Select item 704233	NM_018117.12(WDR11):c.3437+8G>A	WDR11	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 2635649	NM_018117.12(WDR11):c.3607G>A (p.Ala1203Thr)	WDR11 (A1203T)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance