WDR86[gene] and "single gene"[properties] - ClinVar

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Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3190310	NM_198285.3(WDR86):c.913G>A (p.Gly305Arg)	WDR86 (G177R +2 more)	Single nucleotide variant (nonsense +2 more)	not specified	GUncertain significance
Select item 2513046	NM_198285.3(WDR86):c.848A>G (p.Tyr283Cys)	WDR86 (Y155C +1 more)	Single nucleotide variant (synonymous variant +2 more)	not specified	GUncertain significance
Select item 3190309	NM_198285.3(WDR86):c.826C>T (p.Arg276Cys)	WDR86 (R148C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2520615	NM_198285.3(WDR86):c.805C>T (p.Arg269Cys)	WDR86 (A290V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190308	NM_198285.3(WDR86):c.769G>A (p.Val257Ile)	WDR86 (R278H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2330104	NM_198285.3(WDR86):c.764G>C (p.Arg255Thr)	WDR86 (R255T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190307	NM_198285.3(WDR86):c.737G>A (p.Arg246Gln)	WDR86 (R118Q +1 more)	Single nucleotide variant (synonymous variant +2 more)	not specified	GUncertain significance
Select item 2281642	NM_198285.3(WDR86):c.712G>C (p.Val238Leu)	WDR86 (V110L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300742	NM_198285.3(WDR86):c.706G>A (p.Gly236Ser)	WDR86 (G236S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190306	NM_198285.3(WDR86):c.703C>T (p.Arg235Trp)	WDR86 (R107W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377449	NM_198285.3(WDR86):c.697G>A (p.Glu233Lys)	WDR86 (E105K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190305	NM_198285.3(WDR86):c.671G>C (p.Ser224Thr)	WDR86 (S96T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190304	NM_198285.3(WDR86):c.652C>T (p.Arg218Cys)	WDR86 (R90C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402469	NM_198285.3(WDR86):c.638C>T (p.Thr213Ile)	WDR86 (T213I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305139	NM_198285.3(WDR86):c.613G>T (p.Gly205Cys)	WDR86 (G77C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2210357	NM_198285.3(WDR86):c.608C>T (p.Thr203Met)	WDR86 (T75M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549881	NM_198285.3(WDR86):c.568C>T (p.Arg190Trp)	WDR86 (R190W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354450	NM_198285.3(WDR86):c.505G>A (p.Gly169Ser)	WDR86 (G41S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387704	NM_198285.3(WDR86):c.487G>A (p.Gly163Arg)	WDR86 (G163R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372392	NM_198285.3(WDR86):c.481G>A (p.Ala161Thr)	WDR86 (A33T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258882	NM_198285.3(WDR86):c.416G>C (p.Cys139Ser)	WDR86 (C11S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317570	NM_198285.3(WDR86):c.409C>T (p.Arg137Cys)	WDR86 (R9C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190303	NM_198285.3(WDR86):c.350G>A (p.Arg117Gln)	WDR86 (R117Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2216752	NM_198285.3(WDR86):c.290C>T (p.Thr97Met)	WDR86 (T97M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2291144	NM_198285.3(WDR86):c.280C>G (p.Arg94Gly)	WDR86 (R94G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2214314	NM_198285.3(WDR86):c.259G>A (p.Gly87Arg)	WDR86 (G87R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2313267	NM_198285.3(WDR86):c.224C>T (p.Ala75Val)	WDR86 (A75V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2310939	NM_198285.3(WDR86):c.209C>A (p.Ala70Asp)	WDR86 (A70D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2375104	NM_198285.3(WDR86):c.197A>T (p.Glu66Val)	WDR86 (E66V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190302	NM_198285.3(WDR86):c.182C>A (p.Thr61Asn)	WDR86 (T61N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3332977	NM_198285.3(WDR86):c.176A>T (p.Tyr59Phe)	WDR86 (Y59F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 31