"PreventionGenetics, part of Exact Sciences"[submitter] AND "WDR1"[gen - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1086883	NM_017491.5(WDR1):c.1587T>C (p.Tyr529=)	WDR1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3055766	NM_017491.5(WDR1):c.1569+10G>T	WDR1	Single nucleotide variant (intron variant)	WDR1-related disorder	GLikely benign
Select item 1652910	NM_017491.5(WDR1):c.1500C>T (p.Asp500=)	WDR1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1643060	NM_017491.5(WDR1):c.1440G>A (p.Lys480=)	WDR1	Single nucleotide variant (synonymous variant)	WDR1-related disorder +1 more	GLikely benign
Select item 973740	NM_017491.5(WDR1):c.1433C>T (p.Thr478Met)	WDR1 (T338M +1 more)	Single nucleotide variant (missense variant)	WDR1-related disorder +1 more	GLikely benign
Select item 1622171	NM_017491.5(WDR1):c.1395+8G>A	WDR1	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 1164375	NM_017491.5(WDR1):c.1338C>T (p.Tyr446=)	WDR1	Single nucleotide variant (synonymous variant)	WDR1-related disorder +1 more	GBenign/Likely benign
Select item 721980	NM_017491.5(WDR1):c.1284+9C>T	WDR1	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 1549703	NM_017491.5(WDR1):c.1245C>T (p.Val415=)	WDR1	Single nucleotide variant (synonymous variant)	WDR1-related disorder +1 more	GLikely benign
Select item 2632449	NM_017491.5(WDR1):c.1186C>T (p.Arg396Trp)	WDR1 (R256W +1 more)	Single nucleotide variant (missense variant)	WDR1-related disorder	GUncertain significance
Select item 738527	NM_017491.5(WDR1):c.1164G>A (p.Val388=)	WDR1	Single nucleotide variant (synonymous variant)	WDR1-related disorder +1 more	GLikely benign
Select item 1594267	NM_017491.5(WDR1):c.969C>A (p.Ile323=)	WDR1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1533193	NM_017491.5(WDR1):c.894C>T (p.Ser298=)	WDR1	Single nucleotide variant (synonymous variant)	WDR1-related disorder +1 more	GLikely benign
Select item 1354319	NM_017491.5(WDR1):c.802G>A (p.Val268Met)	WDR1 (V268M +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1164640	NM_017491.5(WDR1):c.777G>A (p.Lys259=)	WDR1	Single nucleotide variant (synonymous variant)	WDR1-related disorder +1 more	GBenign/Likely benign
Select item 1109878	NM_017491.5(WDR1):c.732C>T (p.Pro244=)	WDR1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1597677	NM_017491.5(WDR1):c.513G>A (p.Ala171=)	WDR1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 1165989	NM_017491.5(WDR1):c.507C>T (p.Asn169=)	WDR1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 1285066	NM_017491.5(WDR1):c.489C>G (p.Ala163=)	WDR1	Single nucleotide variant (synonymous variant +1 more)	WDR1-related disorder +1 more	GLikely benign
Select item 1581495	NM_017491.5(WDR1):c.453C>T (p.Ser151=)	WDR1	Single nucleotide variant (synonymous variant +1 more)	WDR1-related disorder +1 more	GLikely benign
Select item 722768	NM_017491.5(WDR1):c.414T>A (p.Ser138=)	WDR1	Single nucleotide variant (synonymous variant +1 more)	WDR1-related disorder +1 more	GLikely benign
Select item 2632055	NM_017491.5(WDR1):c.398G>C (p.Trp133Ser)	WDR1 (W133S)	Single nucleotide variant (missense variant +1 more)	WDR1-related disorder	GUncertain significance
Select item 1616135	NM_017491.5(WDR1):c.183G>C (p.Val61=)	WDR1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 2049170	NM_017491.5(WDR1):c.33C>T (p.Ser11=)	WDR1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2200546	NM_017491.5(WDR1):c.21G>A (p.Lys7=)	WDR1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign

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Items: 25