"PreventionGenetics, part of Exact Sciences"[submitter] AND "WDR4"[gen - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 2059339	NM_018669.6(WDR4):c.1149A>G (p.Leu383=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 1566816	NM_018669.6(WDR4):c.1122G>A (p.Lys374=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign
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 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 1288640	NM_018669.6(WDR4):c.1089C>T (p.Ala363=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 3040371	NM_018669.6(WDR4):c.1071C>A (p.Phe357Leu)	WDR4 (F211L +2 more)	Single nucleotide variant (missense variant +1 more)	WDR4-related disorder +1 more	GUncertain significance
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 +1 more	GLikely benign
Select item 1247972	NM_018669.6(WDR4):c.891C>T (p.Phe297=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 2065828	NM_018669.6(WDR4):c.837G>A (p.Gln279=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 2062624	NM_018669.6(WDR4):c.789C>T (p.Asp263=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 2186781	NM_018669.6(WDR4):c.723C>T (p.Pro241=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 2074642	NM_018669.6(WDR4):c.704T>C (p.Leu235Pro)	WDR4 (L89P +1 more)	Single nucleotide variant (missense variant +1 more)	WDR4-related disorder +1 more	GLikely benign
Select item 2059381	NM_018669.6(WDR4):c.613C>T (p.Leu205=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 2055144	NM_018669.6(WDR4):c.596C>T (p.Thr199Ile)	WDR4 (T199I +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GLikely benign
Select item 2053306	NM_018669.6(WDR4):c.586G>A (p.Val196Met)	WDR4 (V196M +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 2055098	NM_018669.6(WDR4):c.528G>A (p.Ala176=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 2144800	NM_018669.6(WDR4):c.486T>G (p.Thr162=)	WDR4	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 3014894	NM_018669.6(WDR4):c.433C>T (p.Leu145=)	WDR4	Single nucleotide variant (synonymous variant +2 more)	not provided +1 more	GLikely benign
Select item 2635103	NM_018669.6(WDR4):c.410G>A (p.Cys137Tyr)	WDR4 (C137Y)	Single nucleotide variant (missense variant +2 more)	WDR4-related disorder	GUncertain significance
Select item 1922002	NM_018669.6(WDR4):c.301G>C (p.Val101Leu)	WDR4 (V101L)	Single nucleotide variant (missense variant +2 more)	WDR4-related disorder +2 more	GLikely benign
Select item 2056254	NM_018669.6(WDR4):c.183C>T (p.Ser61=)	WDR4	Single nucleotide variant (synonymous variant +2 more)	not provided +1 more	GLikely benign
Select item 3014897	NM_018669.6(WDR4):c.105C>T (p.Leu35=)	WDR4	Single nucleotide variant (synonymous variant +2 more)	not provided +1 more	GLikely benign
Select item 1562835	NM_018669.6(WDR4):c.70G>T (p.Ala24Ser)	WDR4 (A24S)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GBenign/Likely benign
Select item 2720648	NM_018669.6(WDR4):c.33G>C (p.Gly11=)	WDR4	Single nucleotide variant (synonymous variant +2 more)	WDR4-related disorder +1 more	GLikely benign

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 25