ClinVar Miner

List of variants in gene F8 reported by CeGaT Center for Human Genetics Tuebingen

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Gene type:
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Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_000132.4(F8):c.102C>T (p.Asp34=) rs1800283 0.00070
NM_000132.4(F8):c.396A>C (p.Glu132Asp) rs137852388 0.00018
NM_000132.4(F8):c.2696G>A (p.Ser899Asn) rs145089334 0.00008
NM_000132.4(F8):c.4442T>C (p.Leu1481Pro) rs1800294 0.00007
NM_000132.4(F8):c.6374G>C (p.Ser2125Thr) rs782363141 0.00005
NM_000132.4(F8):c.2550G>T (p.Leu850=) rs782777398 0.00002
NM_000132.4(F8):c.5063C>T (p.Ser1688Leu) rs782235155 0.00001
NM_000132.4(F8):c.5122C>T (p.Arg1708Cys) rs111033613 0.00001
NM_000132.4(F8):c.1373G>A (p.Arg458His)
NM_000132.4(F8):c.1551G>A (p.Leu517=) rs2073369309
NM_000132.4(F8):c.1835G>T (p.Arg612Leu) rs782473762
NM_000132.4(F8):c.2006C>T (p.Ser669Phe)
NM_000132.4(F8):c.2113+471_2113+473dup
NM_000132.4(F8):c.2727A>G (p.Pro909=)
NM_000132.4(F8):c.2954C>T (p.Ser985Leu)
NM_000132.4(F8):c.3106G>C (p.Gly1036Arg)
NM_000132.4(F8):c.3263C>T (p.Thr1088Ile)
NM_000132.4(F8):c.4254T>A (p.Ile1418=)
NM_000132.4(F8):c.5120C>T (p.Pro1707Leu)
NM_000132.4(F8):c.5143C>A (p.Arg1715=) rs137852439
NM_000132.4(F8):c.5587-93C>T rs1264918703
NM_000132.4(F8):c.5851T>C (p.Leu1951=)
NM_000132.4(F8):c.5999-270C>G
NM_000132.4(F8):c.6483T>A (p.Pro2161=)
NM_000132.4(F8):c.6547A>G (p.Met2183Val) rs781797728
NM_000132.4(F8):c.6720T>G (p.Pro2240=)

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