Related gene-specific medical variations for Gene (Select 23087) - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3328711	NM_171982.5(TRIM35):c.26C>T (p.Pro9Leu)	PTK2B, TRIM35 (P9L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182396	NM_171982.5(TRIM35):c.433C>T (p.Arg145Trp)	LOC130000066, PTK2B +1 more (R145W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182394	NM_171982.5(TRIM35):c.259G>A (p.Ala87Thr)	PTK2B, TRIM35 (A87T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525528	NM_171982.5(TRIM35):c.8G>A (p.Arg3Gln)	PTK2B, TRIM35 (R3Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460440	NM_171982.5(TRIM35):c.157G>T (p.Val53Leu)	LOC130000067, PTK2B +1 more (V53L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459670	NM_171982.5(TRIM35):c.421G>A (p.Ala141Thr)	LOC130000066, PTK2B +1 more (A141T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382201	NM_171982.5(TRIM35):c.17A>G (p.Asp6Gly)	PTK2B, TRIM35 (D6G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370930	NM_171982.5(TRIM35):c.305G>A (p.Arg102His)	PTK2B, TRIM35 +1 more (R102H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280649	NM_171982.5(TRIM35):c.188G>A (p.Arg63His)	LOC130000067, PTK2B +1 more (R63H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 773402	NM_171982.5(TRIM35):c.363C>T (p.Cys121=)	LOC130000066, PTK2B +1 more	Single nucleotide variant (synonymous variant)	not provided	GBenign