Related gene-specific medical variations for Gene (Select 113419) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3176388	NM_144582.3(TEX261):c.64G>A (p.Ala22Thr)	LOC129934054, TEX261 (A22T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176387	NM_144582.3(TEX261):c.29T>C (p.Leu10Pro)	LOC129934054, TEX261 (L10P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance