List of variants in gene F10 reported as uncertain significance for hematologic disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 46

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HGVS	dbSNP	gnomAD frequency
NM_000504.4(F10):c.60C>T (p.Leu20=)	rs3211718	0.00507
NM_000504.4(F10):c.424G>A (p.Glu142Lys)	rs61753266	0.00347
NM_000504.4(F10):c.1032C>T (p.Pro344=)	rs41286610	0.00106
NM_000504.4(F10):c.646G>A (p.Asp216Asn)	rs144711550	0.00031
NM_000504.4(F10):c.947A>G (p.Lys316Arg)	rs144679674	0.00030
NM_000504.4(F10):c.872G>A (p.Arg291Gln)	rs149212700	0.00028
NM_000504.4(F10):c.57G>A (p.Leu19=)	rs370154986	0.00021
NM_000504.4(F10):c.460G>A (p.Gly154Arg)	rs149285827	0.00016
NM_000504.4(F10):c.747+11G>A	rs376728587	0.00016
NM_000504.4(F10):c.747+8T>C	rs200618182	0.00016
NM_000504.4(F10):c.1222G>A (p.Asp408Asn)	rs369409423	0.00010
NM_000504.4(F10):c.257-12C>T	rs372691873	0.00010
NM_000504.4(F10):c.142A>C (p.Met48Leu)	rs201731360	0.00009
NM_000504.4(F10):c.7C>T (p.Arg3Cys)	rs149972574	0.00008
NM_000504.4(F10):c.1226C>T (p.Thr409Ile)	rs775241064	0.00006
NM_000504.4(F10):c.878C>T (p.Thr293Met)	rs752412971	0.00005
NM_000504.4(F10):c.1415C>T (p.Pro472Leu)	rs1315933127	0.00004
NM_000504.3(F10):c.-60G>A	rs3212993	0.00003
NM_000504.4(F10):c.348C>T (p.Phe116=)	rs747030511	0.00003
NM_000504.4(F10):c.1215C>T (p.Ala405=)	rs770904651	0.00001
NM_000504.4(F10):c.261C>T (p.Gly87=)	rs763365831	0.00001
NM_000504.4(F10):c.318G>C (p.Gly106=)	rs567909277	0.00001
NM_000504.4(F10):c.535C>T (p.Arg179Cys)	rs1277295882	0.00001
NM_000504.4(F10):c.80G>A (p.Arg27His)	rs1263735827	0.00001
NM_000504.4(F10):c.-10C>G	rs757542867
NM_000504.4(F10):c.1043G>A (p.Trp348Ter)	rs1566922655
NM_000504.4(F10):c.107C>A (p.Ala36Glu)	rs2036405879
NM_000504.4(F10):c.1094G>C (p.Gly365Ala)
NM_000504.4(F10):c.1237G>A (p.Asp413Asn)	rs1595099677
NM_000504.4(F10):c.1321G>A (p.Glu441Lys)	rs1305872315
NM_000504.4(F10):c.1325G>A (p.Gly442Asp)	rs1233330150
NM_000504.4(F10):c.1347C>T (p.Tyr449=)	rs1432439347
NM_000504.4(F10):c.1387G>C (p.Asp463His)	rs1476602298
NM_000504.4(F10):c.1406G>A (p.Arg469Lys)	rs771971250
NM_000504.4(F10):c.152G>A (p.Gly51Glu)	rs751782758
NM_000504.4(F10):c.160G>A (p.Glu54Lys)	rs121964939
NM_000504.4(F10):c.231G>C (p.Thr77=)	rs201932014
NM_000504.4(F10):c.241T>G (p.Trp81Gly)	rs1595092916
NM_000504.4(F10):c.28C>T (p.Leu10Phe)	rs2142244681
NM_000504.4(F10):c.584C>G (p.Pro195Arg)	rs886050002
NM_000504.4(F10):c.633C>G (p.Thr211=)	rs140852978
NM_000504.4(F10):c.702G>C (p.Arg234Ser)	rs1595096266
NM_000504.4(F10):c.829T>A (p.Cys277Ser)	rs2138554252
NM_000504.4(F10):c.84G>T (p.Arg28Ser)	rs1212018525
NM_000504.4(F10):c.89A>G (p.Gln30Arg)	rs2142252077
NM_000504.4(F10):c.916G>A (p.Glu306Lys)	rs1366354349

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