ClinVar Miner

List of variants in gene F5 reported as uncertain significance for coagulation protein disease

Included ClinVar conditions (43):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 95
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HGVS dbSNP
NM_000130.4(F5):c.*104A>C rs886045540
NM_000130.4(F5):c.*1170G>A rs191866237
NM_000130.4(F5):c.*1290G>A rs9332677
NM_000130.4(F5):c.*1432C>T rs886045536
NM_000130.4(F5):c.*1488T>C rs75764442
NM_000130.4(F5):c.*149C>G rs534748300
NM_000130.4(F5):c.*157A>T rs886045539
NM_000130.4(F5):c.*1780G>T rs559071301
NM_000130.4(F5):c.*1939T>C rs886045535
NM_000130.4(F5):c.*2053G>C rs886045534
NM_000130.4(F5):c.*216T>A rs186962725
NM_000130.4(F5):c.*363T>G rs115882472
NM_000130.4(F5):c.*390C>T rs886045538
NM_000130.4(F5):c.*396C>A rs181328696
NM_000130.4(F5):c.*400C>G rs886045537
NM_000130.4(F5):c.*441C>T rs188490117
NM_000130.4(F5):c.*476C>T rs72708017
NM_000130.4(F5):c.*581C>A rs180742904
NM_000130.4(F5):c.*598T>G rs544753372
NM_000130.4(F5):c.*762G>A rs753366128
NM_000130.4(F5):c.*838T>C rs376103455
NM_000130.4(F5):c.*891A>G rs9332674
NM_000130.4(F5):c.-110C>A rs886045552
NM_000130.4(F5):c.-40T>C rs41272465
NM_000130.4(F5):c.-84G>A rs543172813
NM_000130.4(F5):c.1034G>A (p.Arg345Gln) rs201078171
NM_000130.4(F5):c.1106C>T (p.Ala369Val) rs200934105
NM_000130.4(F5):c.111T>A (p.Ala37=) rs537081933
NM_000130.4(F5):c.1300G>A (p.Val434Met) rs574610215
NM_000130.4(F5):c.1321C>T (p.Arg441Cys) rs747006175
NM_000130.4(F5):c.1391C>T (p.Thr464Ile) rs141768227
NM_000130.4(F5):c.1545C>T (p.Ile515=) rs886045551
NM_000130.4(F5):c.1624A>G (p.Ile542Val) rs776949074
NM_000130.4(F5):c.1659G>A (p.Glu553=) rs370739570
NM_000130.4(F5):c.165T>C (p.Asn55=) rs781434840
NM_000130.4(F5):c.1785G>A (p.Glu595=) rs112333778
NM_000130.4(F5):c.1975G>A (p.Gly659Arg)
NM_000130.4(F5):c.2042A>G (p.Asp681Gly) rs886045550
NM_000130.4(F5):c.2222A>G (p.Asn741Ser) rs144979314
NM_000130.4(F5):c.2241_2243AGA[2] (p.Glu750del) rs575766548
NM_000130.4(F5):c.2864G>T (p.Ser955Ile) rs199507543
NM_000130.4(F5):c.2868T>C (p.Tyr956=) rs149067268
NM_000130.4(F5):c.2906A>G (p.Asn969Ser) rs9332604
NM_000130.4(F5):c.3211C>T (p.His1071Tyr) rs146408488
NM_000130.4(F5):c.3255A>C (p.Thr1085=) rs6006
NM_000130.4(F5):c.3261C>G (p.Pro1087=) rs886045549
NM_000130.4(F5):c.3307A>T (p.Asn1103Tyr) rs886045548
NM_000130.4(F5):c.3311C>A (p.Ser1104Tyr) rs188882337
NM_000130.4(F5):c.333C>A (p.Ser111Arg)
NM_000130.4(F5):c.3402C>A (p.Asp1134Glu) rs373880789
NM_000130.4(F5):c.3442T>C (p.Ser1148Pro) rs369276714
NM_000130.4(F5):c.3455A>C (p.Glu1152Ala) rs543751483
NM_000130.4(F5):c.358A>G (p.Ser120Gly)
NM_000130.4(F5):c.3801T>C (p.Leu1267=) rs559683767
NM_000130.4(F5):c.3851C>T (p.Thr1284Ile) rs139573207
NM_000130.4(F5):c.3949G>A (p.Gly1317Ser) rs149048805
NM_000130.4(F5):c.4035A>G (p.Gln1345=) rs886045547
NM_000130.4(F5):c.4309A>T (p.Thr1437Ser) rs115148599
NM_000130.4(F5):c.4333A>G (p.Thr1445Ala) rs200204656
NM_000130.4(F5):c.4356C>A (p.Ser1452Arg) rs751749207
NM_000130.4(F5):c.437G>A (p.Arg146Gln) rs145625079
NM_000130.4(F5):c.4405T>C (p.Ser1469Pro) rs144262027
NM_000130.4(F5):c.4633C>A (p.Pro1545Thr)
NM_000130.4(F5):c.4744T>A (p.Tyr1582Asn)
NM_000130.4(F5):c.4835A>T (p.Asp1612Val) rs141589936
NM_000130.4(F5):c.4959T>A (p.Asp1653Glu) rs886045546
NM_000130.4(F5):c.4972-14A>C rs763080313
NM_000130.4(F5):c.5054C>G (p.Thr1685Ser) rs6011
NM_000130.4(F5):c.5124C>T (p.Tyr1708=) rs199568344
NM_000130.4(F5):c.5209-12_5209-11delCT rs886045545
NM_000130.4(F5):c.524A>G (p.His175Arg) rs201510575
NM_000130.4(F5):c.5265A>G (p.Ile1755Met)
NM_000130.4(F5):c.5308G>A (p.Val1770Ile) rs374815777
NM_000130.4(F5):c.5332G>C (p.Glu1778Gln) rs886045544
NM_000130.4(F5):c.538G>A (p.Glu180Lys) rs143152035
NM_000130.4(F5):c.5419+11C>G rs6008
NM_000130.4(F5):c.5490G>A (p.Leu1830=) rs149092241
NM_000130.4(F5):c.5534A>G (p.His1845Arg) rs200865371
NM_000130.4(F5):c.5558G>T (p.Gly1853Val) rs182566496
NM_000130.4(F5):c.5589C>A (p.Pro1863=) rs148772659
NM_000130.4(F5):c.5646G>A (p.Trp1882Ter) rs1557908012
NM_000130.4(F5):c.5721T>C (p.Cys1907=) rs886045543
NM_000130.4(F5):c.5788+4A>T rs759428783
NM_000130.4(F5):c.6164G>A (p.Arg2055Gln) rs886045542
NM_000130.4(F5):c.6309G>A (p.Leu2103=) rs35369423
NM_000130.4(F5):c.6360G>A (p.Lys2120=) rs757104503
NM_000130.4(F5):c.6459T>C (p.Tyr2153=) rs773618429
NM_000130.4(F5):c.6589A>G (p.Ile2197Val) rs372005449
NM_000130.4(F5):c.6629A>T (p.Gln2210Leu) rs886045541
NM_000130.4(F5):c.738A>G (p.Thr246=) rs375739973
NM_000130.4(F5):c.773T>C (p.Leu258Pro)
NM_000130.4(F5):c.885C>T (p.Thr295=) rs148752831
NM_000130.4(F5):c.886G>A (p.Ala296Thr) rs748350385
NM_000130.4(F5):c.936C>T (p.Thr312=) rs758832130
NM_000130.4(F5):c.996A>C (p.Lys332Asn)

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