ClinVar Miner

List of variants in gene F5 reported as likely benign for not provided

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Gene type:
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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_000130.5(F5):c.1242A>G (p.Lys414=) rs6035 0.08632
NM_000130.5(F5):c.6309G>A (p.Leu2103=) rs35369423 0.00361
NM_000130.5(F5):c.4923C>T (p.Leu1641=) rs116809837 0.00272
NM_000130.5(F5):c.3162A>C (p.Glu1054Asp) rs149026031 0.00216
NM_000130.5(F5):c.1539A>G (p.Arg513=) rs140627208 0.00148
NM_000130.5(F5):c.5054C>G (p.Thr1685Ser) rs6011 0.00144
NM_000130.5(F5):c.5245C>G (p.Leu1749Val) rs6034 0.00144
NM_000130.5(F5):c.2222A>G (p.Asn741Ser) rs144979314 0.00140
NM_000130.5(F5):c.2835G>A (p.Gly945=) rs370927080 0.00026
NM_000130.5(F5):c.2868T>C (p.Tyr956=) rs149067268 0.00025
NM_000130.5(F5):c.4641T>C (p.Asp1547=) rs138504020 0.00016
NM_000130.5(F5):c.1374A>G (p.Glu458=) rs150708584 0.00010
NM_000130.5(F5):c.1569T>A (p.Leu523=) rs1398320157 0.00001
NM_000130.5(F5):c.3939C>T (p.Ser1313=) rs1445744008 0.00001
NM_000130.5(F5):c.5717-8T>C rs763130267 0.00001
NM_000130.5(F5):c.1397-4T>C rs1571581824
NM_000130.5(F5):c.1572A>G (p.Leu524=) rs1304442049
NM_000130.5(F5):c.251-6del
NM_000130.5(F5):c.4011A>T (p.Thr1337=) rs1571573291
NM_000130.5(F5):c.510C>T (p.His170=)
NM_000130.5(F5):c.5541G>A (p.Gln1847=) rs1571564181
NM_000130.5(F5):c.6087G>A (p.Glu2029=) rs549481773

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