Related gene-specific medical variations for Gene (Select 130000067) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 2280649	NM_171982.5(TRIM35):c.188G>A (p.Arg63His)	LOC130000067, PTK2B +1 more (R63H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance