ClinVar Miner

List of variants in gene NUP155 studied for atrial fibrillation, familial, 15

Included ClinVar conditions (1):
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Total variants: 7
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HGVS dbSNP gnomAD frequency
NM_153485.3(NUP155):c.201G>A (p.Leu67=) rs217852 0.96886
NM_153485.3(NUP155):c.1304A>G (p.Asn435Ser) rs147902256 0.00081
NM_153485.3(NUP155):c.1204G>A (p.Val402Met) rs148814027 0.00052
NM_153485.3(NUP155):c.1348A>G (p.Met450Val) rs374935918 0.00003
NM_153485.3(NUP155):c.3226C>T (p.Arg1076Cys) rs376467373 0.00001
NM_153485.3(NUP155):c.1172G>A (p.Arg391His) rs587777339
NM_153485.3(NUP155):c.3247C>T (p.Arg1083Trp)

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