|
NM_000132.4(F8):c.1444-22T>C
|
rs5986899
|
0.00999
|
|
NM_000132.4(F8):c.1508G>A (p.Arg503His)
|
rs35383156
|
0.00563
|
|
NM_000132.4(F8):c.2994T>G (p.His998Gln)
|
rs149853218
|
0.00388
|
|
NM_000132.4(F8):c.389-9C>T
|
rs35621875
|
0.00356
|
|
NM_000132.4(F8):c.3621C>T (p.His1207=)
|
rs28370212
|
0.00335
|
|
NM_000132.4(F8):c.2947G>A (p.Val983Ile)
|
rs35295375
|
0.00205
|
|
NM_000132.4(F8):c.3236G>A (p.Arg1079Lys)
|
rs143174629
|
0.00136
|
|
NM_000132.4(F8):c.4467C>G (p.Val1489=)
|
rs35207609
|
0.00134
|
|
NM_000132.4(F8):c.2453C>T (p.Thr818Ile)
|
rs142274278
|
0.00080
|
|
NM_000132.4(F8):c.102C>T (p.Asp34=)
|
rs1800283
|
0.00070
|
|
NM_000132.4(F8):c.3169G>A (p.Glu1057Lys)
|
rs28933673
|
0.00025
|
|
NM_000132.4(F8):c.2383A>G (p.Arg795Gly)
|
rs2228152
|
0.00022
|
|
NM_000132.4(F8):c.396A>C (p.Glu132Asp)
|
rs137852388
|
0.00021
|
|
NM_000132.4(F8):c.6276G>A (p.Val2092=)
|
rs199522131
|
0.00019
|
|
NM_000132.4(F8):c.222G>A (p.Thr74=)
|
rs1232517683
|
0.00011
|
|
NM_000132.4(F8):c.6089G>A (p.Ser2030Asn)
|
rs369414658
|
0.00008
|
|
NM_000132.4(F8):c.6724G>A (p.Val2242Met)
|
rs782654096
|
0.00008
|
|
NM_000132.4(F8):c.1094A>G (p.Tyr365Cys)
|
rs375241473
|
0.00006
|
|
NM_000132.4(F8):c.121G>T (p.Gly41Cys)
|
rs137852379
|
0.00005
|
|
NM_000132.4(F8):c.2150G>A (p.Arg717Gln)
|
rs942909873
|
0.00005
|
|
NM_000132.4(F8):c.748A>G (p.Met250Val)
|
rs781943293
|
0.00005
|
|
NM_000132.4(F8):c.1018G>A (p.Glu340Lys)
|
rs781954986
|
0.00004
|
|
NM_000132.4(F8):c.4828G>T (p.Ala1610Ser)
|
rs782127226
|
0.00004
|
|
NM_000132.4(F8):c.1748A>G (p.Asn583Ser)
|
rs782657516
|
0.00003
|
|
NM_000132.4(F8):c.248C>G (p.Pro83Arg)
|
rs781974394
|
0.00003
|
|
NM_000132.4(F8):c.5144G>A (p.Arg1715Gln)
|
rs781876217
|
0.00003
|
|
NM_000132.4(F8):c.733C>T (p.Arg245Trp)
|
rs781943956
|
0.00003
|
|
NM_000132.4(F8):c.2149C>T (p.Arg717Trp)
|
rs137852435
|
0.00002
|
|
NM_000132.4(F8):c.323A>C (p.Lys108Thr)
|
rs137852384
|
0.00002
|
|
NM_000132.4(F8):c.508C>T (p.Pro170Ser)
|
rs782458440
|
0.00002
|
|
NM_000132.4(F8):c.5123G>A (p.Arg1708His)
|
rs111033614
|
0.00002
|
|
NM_000132.4(F8):c.5999-11G>A
|
rs782132907
|
0.00002
|
|
NM_000132.4(F8):c.1569G>T (p.Leu523=)
|
rs782733685
|
0.00001
|
|
NM_000132.4(F8):c.1648C>T (p.Arg550Cys)
|
rs137852417
|
0.00001
|
|
NM_000132.4(F8):c.1649G>A (p.Arg550His)
|
rs137852418
|
0.00001
|
|
NM_000132.4(F8):c.1660A>G (p.Ser554Gly)
|
rs137852419
|
0.00001
|
|
NM_000132.4(F8):c.1835G>A (p.Arg612His)
|
rs782473762
|
0.00001
|
|
NM_000132.4(F8):c.493C>T (p.Pro165Ser)
|
rs137852393
|
0.00001
|
|
NM_000132.4(F8):c.5063C>T (p.Ser1688Leu)
|
rs782235155
|
0.00001
|
|
NM_000132.4(F8):c.5302C>T (p.Arg1768Cys)
|
rs1046670041
|
0.00001
|
|
NM_000132.4(F8):c.5954G>A (p.Arg1985Gln)
|
rs1490417405
|
0.00001
|
|
NM_000132.4(F8):c.5976G>A (p.Met1992Ile)
|
rs782510443
|
0.00001
|
|
NM_000132.4(F8):c.599A>G (p.Glu200Gly)
|
rs782158761
|
0.00001
|
|
NM_000132.4(F8):c.6304G>A (p.Gly2102Ser)
|
rs200433372
|
0.00001
|
|
NM_000132.4(F8):c.6371A>G (p.Tyr2124Cys)
|
rs137852459
|
0.00001
|
|
NM_000132.4(F8):c.6533G>A (p.Arg2178His)
|
rs137852465
|
0.00001
|
|
NM_000132.4(F8):c.6622C>G (p.Gln2208Glu)
|
rs1472169963
|
0.00001
|
|
NM_000132.4(F8):c.6623A>G (p.Gln2208Arg)
|
rs782198570
|
0.00001
|
|
NM_000132.4(F8):c.6658G>C (p.Ala2220Pro)
|
rs782548763
|
0.00001
|
|
NM_000132.4(F8):c.6932C>A (p.Pro2311His)
|
rs1047644991
|
0.00001
|
|
NM_000132.4(F8):c.6955C>T (p.Pro2319Ser)
|
rs137852374
|
0.00001
|
|
NM_000132.4(F8):c.6967C>T (p.Arg2323Cys)
|
rs137852473
|
0.00001
|
|
NM_000132.4(F8):c.6977G>A (p.Arg2326Gln)
|
rs137852360
|
0.00001
|
|
NM_000132.4(F8):c.940A>G (p.Thr314Ala)
|
rs137852406
|
0.00001
|
|
NM_000132.4(F8):c.979C>G (p.Leu327Val)
|
rs1603435395
|
0.00001
|
|
NM_000132.4(F8):c.101A>T (p.Asp34Val)
|
rs2073764726
|
|
|
NM_000132.4(F8):c.1034T>C (p.Val345Ala)
|
rs1189348665
|
|
|
NM_000132.4(F8):c.1214T>G (p.Ile405Ser)
|
rs28933670
|
|
|
NM_000132.4(F8):c.1247C>T (p.Pro416Leu)
|
rs2523951112
|
|
|
NM_000132.4(F8):c.1331A>G (p.Lys444Arg)
|
rs28937272
|
|
|
NM_000132.4(F8):c.1372C>T (p.Arg458Cys)
|
rs2523950289
|
|
|
NM_000132.4(F8):c.1468A>G (p.Arg490Gly)
|
rs1603435026
|
|
|
NM_000132.4(F8):c.1589A>G (p.Tyr530Cys)
|
rs1557281265
|
|
|
NM_000132.4(F8):c.1636C>T (p.Arg546Trp)
|
rs137852416
|
|
|
NM_000132.4(F8):c.1804C>G (p.Arg602Gly)
|
rs137852424
|
|
|
NM_000132.4(F8):c.1910A>G (p.Asn637Ser)
|
rs2073315379
|
|
|
NM_000132.4(F8):c.2009TCT[2] (p.Phe672del)
|
rs1476178386
|
|
|
NM_000132.4(F8):c.2103G>A (p.Met701Ile)
|
rs2073313787
|
|
|
NM_000132.4(F8):c.2150G>T (p.Arg717Leu)
|
rs942909873
|
|
|
NM_000132.4(F8):c.335C>T (p.Ser112Phe)
|
rs2073620915
|
|
|
NM_000132.4(F8):c.3619_3622del (p.His1207fs)
|
|
|
|
NM_000132.4(F8):c.3637dup (p.Ile1213fs)
|
rs387906450
|
|
|
NM_000132.4(F8):c.409A>G (p.Thr137Ala)
|
|
|
|
NM_000132.4(F8):c.4379del (p.Asn1460fs)
|
rs387906455
|
|
|
NM_000132.4(F8):c.4379dup (p.Asn1460fs)
|
rs387906455
|
|
|
NM_000132.4(F8):c.5186G>A (p.Gly1729Glu)
|
rs1557278259
|
|
|
NM_000132.4(F8):c.5320C>T (p.His1774Tyr)
|
|
|
|
NM_000132.4(F8):c.5399G>A (p.Arg1800His)
|
rs137852442
|
|
|
NM_000132.4(F8):c.5422C>T (p.Leu1808Phe)
|
rs137852445
|
|
|
NM_000132.4(F8):c.5558C>T (p.Ala1853Val)
|
rs28933677
|
|
|
NM_000132.4(F8):c.5587-93C>T
|
rs1264918703
|
|
|
NM_000132.4(F8):c.5598G>A (p.Val1866=)
|
|
|
|
NM_000132.4(F8):c.5815G>C (p.Ala1939Pro)
|
rs1603432979
|
|
|
NM_000132.4(F8):c.5843T>C (p.Leu1948Pro)
|
|
|
|
NM_000132.4(F8):c.5879G>A (p.Arg1960Gln)
|
rs28937294
|
|
|
NM_000132.4(F8):c.592T>G (p.Cys198Gly)
|
rs137852475
|
|
|
NM_000132.4(F8):c.6302A>G (p.His2101Arg)
|
|
|
|
NM_000132.4(F8):c.6400T>C (p.Tyr2134His)
|
rs2523876717
|
|
|
NM_000132.4(F8):c.6429+5G>A
|
rs2072977075
|
|
|
NM_000132.4(F8):c.6506G>A (p.Arg2169His)
|
rs137852461
|
|
|
NM_000132.4(F8):c.6532C>T (p.Arg2178Cys)
|
rs137852464
|
|
|
NM_000132.4(F8):c.6533G>T (p.Arg2178Leu)
|
rs137852465
|
|
|
NM_000132.4(F8):c.6547A>G (p.Met2183Val)
|
rs781797728
|
|
|
NM_000132.4(F8):c.6679G>A (p.Ala2227Thr)
|
rs1342196860
|
|
|
NM_000132.4(F8):c.6685C>T (p.Leu2229Phe)
|
rs1603431508
|
|
|
NM_000132.4(F8):c.6686T>C (p.Leu2229Pro)
|
rs1603431506
|
|
|
NM_000132.4(F8):c.6956dup (p.Leu2320fs)
|
rs1475873048
|
|
|
NM_000132.4(F8):c.6968G>A (p.Arg2323His)
|
rs137852474
|
|
|
NM_000132.4(F8):c.766T>A (p.Tyr256Asn)
|
rs1569559955
|
|
|
NM_000132.4(F8):c.797G>A (p.Gly266Glu)
|
rs137852398
|
|
|
NM_000132.4(F8):c.842C>T (p.Thr281Ile)
|
rs2073444610
|
|
|
NM_000132.4(F8):c.901C>T (p.Arg301Cys)
|
rs1401805753
|
|
|
NM_000132.4(F8):c.935T>C (p.Phe312Ser)
|
rs137852405
|
|
|
NM_000132.4(F8):c.980T>C (p.Leu327Pro)
|
rs137852407
|
|
|
NM_000132.4(F8):c.986G>A (p.Cys329Tyr)
|
rs137852409
|
|
|
Single allele
|
|
|