ClinVar Miner

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

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Total variants: 9
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HGVS dbSNP
GRCh37/hg19 4q35.2(chr4:187182119-187216375)x1
NM_000128.3(F11):c.1560G>T (p.Gly520=) rs794727084
NM_000128.3(F11):c.218+4A>G rs767240420
NM_000128.3(F11):c.484C>T (p.Arg162Cys) rs748139184
NM_000128.3(F11):c.809A>T (p.Lys270Ile) rs121965070
NM_000128.4(F11):c.1858G>C (p.Glu620Gln)
NM_000128.4(F11):c.196C>T (p.Pro66Ser) rs144595035
NM_000128.4(F11):c.434A>G (p.His145Arg)
NM_000128.4(F11):c.581C>T (p.Ala194Val) rs1580079656

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