ClinVar Miner

List of variants in gene F11 reported by Mayo Clinic Laboratories, Mayo Clinic

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Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_000128.4(F11):c.901T>C (p.Phe301Leu) rs121965064 0.00066
NM_000128.4(F11):c.403G>T (p.Glu135Ter) rs121965063 0.00064
NM_000128.4(F11):c.196C>T (p.Pro66Ser) rs144595035 0.00009
NM_000128.4(F11):c.1288G>A (p.Ala430Thr) rs753909969 0.00006
NM_000128.4(F11):c.434A>G (p.His145Arg) rs199657604 0.00005
NM_000128.4(F11):c.802C>T (p.Arg268Cys) rs763496524 0.00005
NM_000128.4(F11):c.1327C>T (p.Arg443Cys) rs369435407 0.00003
NM_000128.4(F11):c.325G>A (p.Ala109Thr) rs768474112 0.00003
NM_000128.4(F11):c.976C>T (p.Arg326Cys) rs28934608 0.00002
NM_000128.4(F11):c.1199C>T (p.Pro400Leu) rs533335580 0.00001
NM_000128.4(F11):c.1480+1G>T rs767037207 0.00001
NM_000128.4(F11):c.1556G>A (p.Trp519Ter) rs201007090 0.00001
NM_000128.4(F11):c.1627G>A (p.Glu543Lys) rs142952627 0.00001
NM_000128.4(F11):c.1727G>A (p.Gly576Glu) rs149873248 0.00001
NM_000128.4(F11):c.419G>A (p.Cys140Tyr) rs281875256 0.00001
NM_000128.4(F11):c.595+3A>G rs933333847 0.00001
NM_000128.4(F11):c.755+2T>C rs1220869989 0.00001
NM_000128.4(F11):c.1443del (p.Ile481fs) rs778810767
NM_000128.4(F11):c.1481-1G>C rs1057516506
NM_000128.4(F11):c.155dup (p.Tyr52Ter) rs1554081886
NM_000128.4(F11):c.1866_1867del (p.Gln623fs) rs1741391592
NM_000128.4(F11):c.295del (p.Ser99fs)
NM_000128.4(F11):c.485G>A (p.Arg162His)

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