ClinVar Miner

List of variants in gene F8 reported as likely benign for not provided

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Total variants: 23
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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.4759G>A (p.Asp1587Asn) rs142347597 0.00029
NM_000132.4(F8):c.1866T>C (p.Leu622=) rs1800290 0.00021
NM_000132.4(F8):c.1064G>A (p.Arg355Gln) rs146581224 0.00019
NM_000132.4(F8):c.2887G>A (p.Asp963Asn) rs199660138 0.00017
NM_000132.4(F8):c.1387C>T (p.His463Tyr) rs193028861 0.00008
NM_000132.4(F8):c.2696G>A (p.Ser899Asn) rs145089334 0.00008
NM_000132.4(F8):c.3996A>G (p.Arg1332=) rs782379086 0.00007
NM_000132.4(F8):c.5200C>T (p.Pro1734Ser) rs782324012 0.00006
NM_000132.4(F8):c.4182G>A (p.Thr1394=) rs782797370 0.00005
NM_000132.4(F8):c.2550G>T (p.Leu850=) rs782777398 0.00002
NM_000132.4(F8):c.1551G>A (p.Leu517=) rs2073369309
NM_000132.4(F8):c.1848T>C (p.Asn616=) rs1603434700
NM_000132.4(F8):c.2727A>G (p.Pro909=)
NM_000132.4(F8):c.2961G>C (p.Glu987Asp)
NM_000132.4(F8):c.312C>A (p.Val104=)
NM_000132.4(F8):c.3263C>T (p.Thr1088Ile)
NM_000132.4(F8):c.3280G>A (p.Glu1094Lys) rs377119670
NM_000132.4(F8):c.4254T>A (p.Ile1418=)
NM_000132.4(F8):c.5999-270C>G
NM_000132.4(F8):c.6483T>A (p.Pro2161=)
NM_000132.4(F8):c.6663C>A (p.Thr2221=)
NM_000132.4(F8):c.6720T>G (p.Pro2240=)

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