ClinVar Miner

List of variants in gene F9 reported as uncertain significance for not specified

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Total variants: 14
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HGVS dbSNP gnomAD frequency
NM_000133.4(F9):c.1345C>T (p.Arg449Trp) rs757996262 0.00009
NM_000133.4(F9):c.1346G>A (p.Arg449Gln) rs143018900 0.00007
NM_000133.4(F9):c.1078T>A (p.Phe360Ile) rs1603267386
NM_000133.4(F9):c.1105C>T (p.Leu369Phe) rs2148367939
NM_000133.4(F9):c.1148T>C (p.Leu383Pro) rs1387119011
NM_000133.4(F9):c.189A>C (p.Glu63Asp) rs762447016
NM_000133.4(F9):c.374G>A (p.Gly125Glu)
NM_000133.4(F9):c.392-7_392-4del rs2148361119
NM_000133.4(F9):c.424G>C (p.Glu142Gln)
NM_000133.4(F9):c.466T>C (p.Ser156Pro)
NM_000133.4(F9):c.613A>G (p.Thr205Ala) rs1603265805
NM_000133.4(F9):c.682G>A (p.Val228Ile)
NM_000133.4(F9):c.971C>A (p.Pro324His)
NM_000133.4(F9):c.997C>T (p.Pro333Ser) rs2148367784

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