ClinVar for MedGen (Select 862706) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3362422	NM_153485.3(NUP155):c.3247C>T (p.Arg1083Trp)	NUP155 (R1019W +2 more)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 15	GUncertain significance
Select item 3242595	NM_153485.3(NUP155):c.1304A>G (p.Asn435Ser)	NUP155 (N376S +1 more)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 15	GUncertain significance
Select item 1180961	NM_153485.3(NUP155):c.201G>A (p.Leu67=)	NUP155	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1032504	NM_153485.3(NUP155):c.3226C>T (p.Arg1076Cys)	NUP155 (R1017C +2 more)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 15	GUncertain significance
Select item 870608	NM_153485.3(NUP155):c.1204G>A (p.Val402Met)	NUP155 (V343M +1 more)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 15	GUncertain significance
Select item 127142	NM_153485.3(NUP155):c.1172G>A (p.Arg391His)	NUP155 (R391H +1 more)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 15	GPathogenic

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