ClinVar Miner

List of variants in gene F9 reported as uncertain significance for coagulation protein disease

Included ClinVar conditions (68):
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Gene type:
ClinVar version:
Total variants: 49
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HGVS dbSNP gnomAD frequency
NM_000133.4(F9):c.*799A>T rs772966694 0.00978
NM_000133.4(F9):c.19A>T (p.Ile7Phe) rs150190385 0.00086
NM_000133.4(F9):c.*293C>T rs747670394 0.00048
NM_000133.4(F9):c.*794A>G rs1057515800 0.00031
NM_000133.4(F9):c.769G>A (p.Val257Ile) rs200608775 0.00010
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.*621G>A rs1278613777 0.00005
NM_000133.4(F9):c.*1122C>A rs907681842 0.00004
NM_000133.4(F9):c.582T>G (p.Thr194=) rs754155651 0.00004
NM_000133.4(F9):c.391+4A>G rs749754992 0.00003
NM_000133.4(F9):c.485G>A (p.Arg162Gln) rs779281053 0.00003
NM_000133.4(F9):c.*523A>G rs921041074 0.00002
NM_000133.4(F9):c.54C>T (p.Cys18=) rs1337284408 0.00002
NM_000133.4(F9):c.*1283C>G rs1295265700 0.00001
NM_000133.4(F9):c.*197G>A rs1057515798 0.00001
NM_000133.4(F9):c.1210A>G (p.Arg404Gly) rs1390673858 0.00001
NM_000133.4(F9):c.122T>G (p.Leu41Arg) rs371373268 0.00001
NM_000133.4(F9):c.60A>G (p.Leu20=) rs762082146 0.00001
NC_000023.10:g.(?_138612860)_(138643034_?)dup
NM_000133.3(F9):c.-34A>G rs1927322453
NM_000133.4(F9):c.-19C>G rs761036720
NM_000133.4(F9):c.1046G>A (p.Gly349Glu) rs1928113004
NM_000133.4(F9):c.1073G>C (p.Arg358Thr)
NM_000133.4(F9):c.1147C>G (p.Leu383Val) rs1677128088
NM_000133.4(F9):c.1148T>C (p.Leu383Pro) rs1387119011
NM_000133.4(F9):c.1213G>T (p.Asp405Tyr)
NM_000133.4(F9):c.1255G>A (p.Val419Met) rs1928127579
NM_000133.4(F9):c.1276A>C (p.Thr426Pro) rs1928129466
NM_000133.4(F9):c.1292G>T (p.Trp431Leu)
NM_000133.4(F9):c.1332T>C (p.Tyr444=) rs1928132545
NM_000133.4(F9):c.163T>C (p.Phe55Leu) rs759987427
NM_000133.4(F9):c.182A>G (p.Glu61Gly) rs2148356134
NM_000133.4(F9):c.194T>C (p.Met65Thr)
NM_000133.4(F9):c.253-3T>C
NM_000133.4(F9):c.364G>A (p.Gly122Arg) rs770120402
NM_000133.4(F9):c.392-7_392-4del rs2148361119
NM_000133.4(F9):c.413A>G (p.Asn138Ser) rs2148361153
NM_000133.4(F9):c.430T>C (p.Phe144Leu) rs2148361174
NM_000133.4(F9):c.44T>A (p.Ile15Asn) rs1927326780
NM_000133.4(F9):c.517G>A (p.Ala173Thr) rs865782271
NM_000133.4(F9):c.520+13A>G rs1603265507
NM_000133.4(F9):c.584T>A (p.Val195Asp) rs374674030
NM_000133.4(F9):c.612T>C (p.Ser204=) rs1199474371
NM_000133.4(F9):c.704C>A (p.Pro235Gln) rs2148362579
NM_000133.4(F9):c.949G>A (p.Ala317Thr)
NM_000133.4(F9):c.960A>C (p.Glu320Asp) rs1489951549
NM_000133.4(F9):c.984C>G (p.Asn328Lys)
Single allele

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