Related gene-specific medical variations for Gene (Select 349136) - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3332978	NM_198285.3(WDR86):c.1055C>T (p.Pro352Leu)	LOC129999646, WDR86 (L179F +2 more)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 3332976	NM_198285.3(WDR86):c.106G>A (p.Asp36Asn)	WDR86, WDR86-AS1 (D36N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3202689	NM_001243351.2(NUB1):c.1495G>A (p.Val499Met)	NUB1, WDR86 (V485M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190312	NM_198285.3(WDR86):c.973G>A (p.Gly325Ser)	LOC129999646, WDR86 (G197S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190311	NM_198285.3(WDR86):c.92T>A (p.Leu31Gln)	WDR86, WDR86-AS1 (L31Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2596529	NM_198285.3(WDR86):c.56A>T (p.Asn19Ile)	WDR86, WDR86-AS1 (N19I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2516068	NM_198285.3(WDR86):c.46G>A (p.Gly16Arg)	WDR86, WDR86-AS1 (G16R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2394683	NM_001243351.2(NUB1):c.1568C>T (p.Ala523Val)	NUB1, WDR86 (A508V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349084	NM_001243351.2(NUB1):c.1654C>T (p.Pro552Ser)	NUB1, WDR86 (P537S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345789	NM_198285.3(WDR86):c.1012C>T (p.Arg338Cys)	LOC129999646, WDR86 (R210C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2334441	NM_198285.3(WDR86):c.1034T>G (p.Leu345Arg)	LOC129999646, WDR86 (L345R +2 more)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 2275665	NM_001243351.2(NUB1):c.1555G>T (p.Val519Phe)	NUB1, WDR86 (V519F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216852	NM_198285.3(WDR86):c.97G>A (p.Gly33Ser)	WDR86, WDR86-AS1 (G33S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2204624	NM_198285.3(WDR86):c.1055C>G (p.Pro352Arg)	LOC129999646, WDR86 (P224R +2 more)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance