ClinVar Miner

List of variants in gene F11 reported as uncertain significance for not provided

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Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_000128.4(F11):c.797G>A (p.Ser266Asn) rs145168351 0.00081
NM_000128.4(F11):c.809A>T (p.Lys270Ile) rs121965070 0.00055
NM_000128.4(F11):c.1858G>C (p.Glu620Gln) rs148054334 0.00010
NM_000128.4(F11):c.803G>A (p.Arg268His) rs201688862 0.00004
NM_000128.4(F11):c.100G>C (p.Asp34His) rs281875267 0.00001
NM_000128.4(F11):c.1727G>A (p.Gly576Glu) rs149873248 0.00001
NM_000128.4(F11):c.484C>T (p.Arg162Cys) rs748139184 0.00001
GRCh37/hg19 4q35.2(chr4:187182119-187216375)x1
NM_000128.4(F11):c.*194TTTG[1]
NM_000128.4(F11):c.1325T>C (p.Leu442Ser)
NM_000128.4(F11):c.1360A>G (p.Ile454Val) rs903458418
NM_000128.4(F11):c.1478C>G (p.Thr493Arg)
NM_000128.4(F11):c.1560G>T (p.Gly520=) rs794727084
NM_000128.4(F11):c.1628A>G (p.Glu543Gly) rs2126787863
NM_000128.4(F11):c.17A>G (p.Gln6Arg)
NM_000128.4(F11):c.1866_1867del (p.Gln623fs)
NM_000128.4(F11):c.206A>G (p.Asp69Gly)
NM_000128.4(F11):c.218+4A>G rs767240420
NM_000128.4(F11):c.448A>G (p.Thr150Ala) rs1740201176
NM_000128.4(F11):c.581C>T (p.Ala194Val) rs1580079656
NM_000128.4(F11):c.596_606delinsTCCCT (p.Ala199_Arg202delinsValPro)
NM_000128.4(F11):c.666T>A (p.Asp222Glu)
NM_000128.4(F11):c.778T>C (p.Ser260Pro)

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