Related gene-specific medical variations for Gene (Select 9631) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3301472	NM_153485.3(NUP155):c.131C>G (p.Ser44Cys)	LOC129993817, NUP155 (S44C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 977374	NM_153485.3(NUP155):c.1348A>G (p.Met450Val)	NUP155 (M391V +1 more)	Single nucleotide variant (missense variant)	Atrial fibrillation	GUncertain significance