NM_000132.4(F8):c.222G>A (p.Thr74=)
|
rs1232517683
|
0.00012
|
NM_000132.4(F8):c.5144G>A (p.Arg1715Gln)
|
rs781876217
|
0.00003
|
NM_000132.4(F8):c.6304G>A (p.Gly2102Ser)
|
rs200433372
|
0.00001
|
NM_000132.4(F8):c.6932C>A (p.Pro2311His)
|
rs1047644991
|
0.00001
|
NM_000132.4(F8):c.101A>T (p.Asp34Val)
|
|
|
NM_000132.4(F8):c.1175C>T (p.Ser392Leu)
|
rs28933668
|
|
NM_000132.4(F8):c.1247C>T (p.Pro416Leu)
|
|
|
NM_000132.4(F8):c.1312A>T (p.Ile438Phe)
|
|
|
NM_000132.4(F8):c.1430G>T (p.Gly477Val)
|
rs2124105158
|
|
NM_000132.4(F8):c.1443+5G>A
|
rs1195283929
|
|
NM_000132.4(F8):c.1444-3C>G
|
rs1603435027
|
|
NM_000132.4(F8):c.1481T>G (p.Ile494Ser)
|
rs137852413
|
|
NM_000132.4(F8):c.1504G>T (p.Val502Phe)
|
rs2073393106
|
|
NM_000132.4(F8):c.1538-18G>A
|
rs1482306571
|
|
NM_000132.4(F8):c.1639T>C (p.Cys547Arg)
|
|
|
NM_000132.4(F8):c.1648C>G (p.Arg550Gly)
|
rs137852417
|
|
NM_000132.4(F8):c.1778T>A (p.Ile593Asn)
|
rs1557280964
|
|
NM_000132.4(F8):c.1808G>A (p.Ser603Asn)
|
|
|
NM_000132.4(F8):c.1825A>C (p.Asn609His)
|
rs2073350730
|
|
NM_000132.4(F8):c.1952A>C (p.His651Pro)
|
rs1569559758
|
|
NM_000132.4(F8):c.2101A>G (p.Met701Val)
|
rs2073313804
|
|
NM_000132.4(F8):c.2161A>C (p.Met721Leu)
|
rs1305924233
|
|
NM_000132.4(F8):c.219C>G (p.Phe73Leu)
|
rs1603436770
|
|
NM_000132.4(F8):c.335C>T (p.Ser112Phe)
|
|
|
NM_000132.4(F8):c.377A>G (p.Lys126Arg)
|
rs1603436639
|
|
NM_000132.4(F8):c.382T>C (p.Ser128Pro)
|
rs1603436638
|
|
NM_000132.4(F8):c.403G>T (p.Asp135Tyr)
|
rs2073597882
|
|
NM_000132.4(F8):c.5093T>C (p.Ile1698Thr)
|
rs2073173387
|
|
NM_000132.4(F8):c.5143C>G (p.Arg1715Gly)
|
rs137852439
|
|
NM_000132.4(F8):c.5219G>T (p.Arg1740Met)
|
rs1444273117
|
|
NM_000132.4(F8):c.5308G>A (p.Glu1770Lys)
|
rs2124000594
|
|
NM_000132.4(F8):c.5417C>T (p.Ser1806Phe)
|
rs1569559523
|
|
NM_000132.4(F8):c.5422C>T (p.Leu1808Phe)
|
rs137852445
|
|
NM_000132.4(F8):c.5527G>A (p.Ala1843Thr)
|
rs1603432996
|
|
NM_000132.4(F8):c.5587-93C>T
|
rs1264918703
|
|
NM_000132.4(F8):c.55A>C (p.Ser19Arg)
|
rs2124174458
|
|
NM_000132.4(F8):c.5696T>C (p.Phe1899Ser)
|
rs1486435006
|
|
NM_000132.4(F8):c.5813A>G (p.His1938Arg)
|
rs1603432981
|
|
NM_000132.4(F8):c.5815G>C (p.Ala1939Pro)
|
rs1603432979
|
|
NM_000132.4(F8):c.5843T>G (p.Leu1948Arg)
|
|
|
NM_000132.4(F8):c.5875A>T (p.Ile1959Phe)
|
rs1411617809
|
|
NM_000132.4(F8):c.592T>G (p.Cys198Gly)
|
rs137852475
|
|
NM_000132.4(F8):c.5939A>G (p.His1980Arg)
|
rs1569559516
|
|
NM_000132.4(F8):c.5941G>A (p.Val1981Met)
|
|
|
NM_000132.4(F8):c.601G>A (p.Gly201Arg)
|
rs1229954426
|
|
NM_000132.4(F8):c.6043T>C (p.Trp2015Arg)
|
rs2073013277
|
|
NM_000132.4(F8):c.606T>G (p.Ser202Arg)
|
rs1603436217
|
|
NM_000132.4(F8):c.6118T>G (p.Cys2040Gly)
|
rs2123993603
|
|
NM_000132.4(F8):c.6273G>A (p.Lys2091=)
|
rs2148584915
|
|
NM_000132.4(F8):c.6278A>T (p.Asp2093Val)
|
rs137852457
|
|
NM_000132.4(F8):c.6296T>A (p.Ile2099Asn)
|
rs1603432784
|
|
NM_000132.4(F8):c.6320G>A (p.Gly2107Asp)
|
rs1190705187
|
|
NM_000132.4(F8):c.640T>G (p.Phe214Val)
|
rs2073563995
|
|
NM_000132.4(F8):c.6485C>T (p.Pro2162Leu)
|
|
|
NM_000132.4(F8):c.650T>C (p.Leu217Pro)
|
rs2124134359
|
|
NM_000132.4(F8):c.650T>G (p.Leu217Arg)
|
rs2124134359
|
|
NM_000132.4(F8):c.6550G>C (p.Glu2184Gln)
|
rs2148568062
|
|
NM_000132.4(F8):c.6593G>A (p.Gly2198Glu)
|
rs2148567338
|
|
NM_000132.4(F8):c.665A>C (p.Asp222Ala)
|
rs137852396
|
|
NM_000132.4(F8):c.6697G>T (p.Gly2233Trp)
|
rs2072692745
|
|
NM_000132.4(F8):c.6719C>T (p.Pro2240Leu)
|
rs1174359623
|
|
NM_000132.4(F8):c.6929C>T (p.Thr2310Ile)
|
rs373079141
|
|
NM_000132.4(F8):c.6959T>G (p.Leu2320Ter)
|
rs2148555597
|
|
NM_000132.4(F8):c.6967C>G (p.Arg2323Gly)
|
rs137852473
|
|
NM_000132.4(F8):c.6975del (p.Arg2326fs)
|
rs2148555575
|
|
NM_000132.4(F8):c.7021G>A (p.Glu2341Lys)
|
rs2072484280
|
|
NM_000132.4(F8):c.74A>G (p.Tyr25Cys)
|
rs2124174443
|
|
NM_000132.4(F8):c.755C>T (p.Thr252Ile)
|
rs1464962436
|
|
NM_000132.4(F8):c.787+5G>C
|
rs1378662017
|
|
NM_000132.4(F8):c.797G>A (p.Gly266Glu)
|
rs137852398
|
|
NM_000132.4(F8):c.83_87del (p.Ala28fs)
|
rs1603437863
|
|
NM_000132.4(F8):c.842C>T (p.Thr281Ile)
|
|
|
NM_000132.4(F8):c.853G>A (p.Val285Met)
|
rs2073444412
|
|
NM_000132.4(F8):c.877C>G (p.His293Asp)
|
rs1569559881
|
|
NM_000132.4(F8):c.881C>G (p.Thr294Arg)
|
|
|
NM_000132.4(F8):c.986G>A (p.Cys329Tyr)
|
rs137852409
|
|
NM_000132.4(F8):c.992T>C (p.Ile331Thr)
|
rs2073442480
|
|