NM_001291867.2(NHS):c.4018T>C (p.Phe1340Leu)
|
rs3747295
|
0.29823
|
NM_001291867.2(NHS):c.1714C>T (p.Pro572Ser)
|
rs150688899
|
0.06491
|
NM_001291867.2(NHS):c.211C>T (p.Pro71Ser)
|
rs398124605
|
0.03116
|
NM_001291867.2(NHS):c.3201T>C (p.Ser1067=)
|
rs56908561
|
0.02903
|
NM_001291867.2(NHS):c.3204A>G (p.Leu1068=)
|
rs56691712
|
0.02899
|
NM_001291867.2(NHS):c.2831A>T (p.His944Leu)
|
rs149244552
|
0.00386
|
NM_001291867.2(NHS):c.3545C>T (p.Pro1182Leu)
|
rs145977627
|
0.00189
|
NM_001291867.2(NHS):c.2593G>A (p.Ala865Thr)
|
rs149609550
|
0.00131
|
NM_001291867.2(NHS):c.828G>A (p.Glu276=)
|
rs147497359
|
0.00096
|
NM_001291867.2(NHS):c.2330T>C (p.Phe777Ser)
|
rs143081492
|
0.00089
|
NM_001291867.2(NHS):c.4832G>C (p.Ser1611Thr)
|
rs140651691
|
0.00086
|
NM_001291867.2(NHS):c.765C>G (p.Pro255=)
|
rs143119491
|
0.00086
|
NM_001291867.2(NHS):c.688G>A (p.Ala230Thr)
|
rs78153843
|
0.00082
|
NM_001291867.2(NHS):c.4168G>A (p.Asp1390Asn)
|
rs142186771
|
0.00081
|
NM_001291867.2(NHS):c.2093G>A (p.Arg698Gln)
|
rs140904281
|
0.00075
|
NM_001291867.2(NHS):c.3929G>T (p.Gly1310Val)
|
rs41304731
|
0.00074
|
NM_001291867.2(NHS):c.1965T>G (p.Pro655=)
|
rs151009077
|
0.00069
|
NM_001291867.2(NHS):c.204A>G (p.Pro68=)
|
rs775588477
|
0.00069
|
NM_001291867.2(NHS):c.4436G>A (p.Ser1479Asn)
|
rs145200841
|
0.00056
|
NM_001291867.2(NHS):c.4666T>A (p.Ser1556Thr)
|
rs2071848
|
0.00055
|
NM_001291867.2(NHS):c.666C>T (p.Cys222=)
|
rs138104885
|
0.00055
|
NM_001291867.2(NHS):c.3374C>T (p.Ser1125Leu)
|
rs145005596
|
0.00053
|
NM_001291867.2(NHS):c.1596G>A (p.Glu532=)
|
rs146437542
|
0.00044
|
NM_001291867.2(NHS):c.258A>G (p.Gly86=)
|
rs1026332275
|
0.00038
|
NM_001291867.2(NHS):c.3785C>T (p.Thr1262Met)
|
rs141013518
|
0.00037
|
NM_001291867.2(NHS):c.1603G>A (p.Val535Met)
|
rs367856134
|
0.00028
|
NM_001291867.2(NHS):c.1748G>A (p.Arg583His)
|
rs143289369
|
0.00028
|
NM_001291867.2(NHS):c.513C>T (p.Leu171=)
|
rs398124610
|
0.00028
|
NM_001291867.2(NHS):c.322G>A (p.Glu108Lys)
|
rs773995388
|
0.00026
|
NM_001291867.2(NHS):c.3959T>C (p.Val1320Ala)
|
rs368703052
|
0.00026
|
NM_001291867.2(NHS):c.1919C>T (p.Thr640Met)
|
rs372391693
|
0.00019
|
NM_001291867.2(NHS):c.4051G>A (p.Asp1351Asn)
|
rs148418212
|
0.00019
|
NM_001291867.2(NHS):c.3310C>T (p.His1104Tyr)
|
rs201263814
|
0.00016
|
NM_001291867.2(NHS):c.1143C>T (p.Cys381=)
|
rs727504042
|
0.00012
|
NM_001291867.2(NHS):c.1228C>G (p.Gln410Glu)
|
rs375878222
|
0.00012
|
NM_001291867.2(NHS):c.2119G>T (p.Ala707Ser)
|
rs184275083
|
0.00012
|
NM_001291867.2(NHS):c.1760T>C (p.Met587Thr)
|
rs187739639
|
0.00011
|
NM_001291867.2(NHS):c.2905G>A (p.Ala969Thr)
|
rs762685365
|
0.00009
|
NM_001291867.2(NHS):c.766C>G (p.Leu256Val)
|
rs200598087
|
0.00009
|
NM_001291867.2(NHS):c.4082C>T (p.Ser1361Leu)
|
rs766379688
|
0.00008
|
NM_001291867.2(NHS):c.1175G>A (p.Arg392Gln)
|
rs372969054
|
0.00007
|
NM_001291867.2(NHS):c.2204G>A (p.Arg735His)
|
rs193921046
|
0.00006
|
NM_001291867.2(NHS):c.618G>A (p.Pro206=)
|
rs200952266
|
0.00005
|
NM_001291867.2(NHS):c.2663T>C (p.Met888Thr)
|
rs200321491
|
0.00004
|
NM_001291867.2(NHS):c.2791G>T (p.Asp931Tyr)
|
rs192848792
|
0.00004
|
NM_001291867.2(NHS):c.2047G>A (p.Val683Met)
|
rs587780403
|
0.00003
|
NM_001291867.2(NHS):c.2732A>G (p.Glu911Gly)
|
rs189687959
|
0.00003
|
NM_001291867.2(NHS):c.1929G>A (p.Ser643=)
|
rs143564715
|
0.00002
|
NM_001291867.2(NHS):c.2683G>A (p.Ala895Thr)
|
rs770236873
|
0.00002
|
NM_001291867.2(NHS):c.3141C>T (p.Pro1047=)
|
rs777688578
|
0.00002
|
NM_001291867.2(NHS):c.4043G>A (p.Arg1348His)
|
rs141525588
|
0.00002
|
NM_001291867.2(NHS):c.4153G>A (p.Ala1385Thr)
|
rs1192248368
|
0.00002
|
NM_001291867.2(NHS):c.612C>T (p.Arg204=)
|
rs777799752
|
0.00001
|
NM_001291867.2(NHS):c.*3008T>A
|
|
|
NM_001291867.2(NHS):c.1089T>C (p.Ile363=)
|
|
|
NM_001291867.2(NHS):c.1326C>T (p.Ser442=)
|
|
|
NM_001291867.2(NHS):c.1386G>A (p.Arg462=)
|
|
|
NM_001291867.2(NHS):c.1443C>G (p.Gly481=)
|
|
|
NM_001291867.2(NHS):c.1471G>A (p.Asp491Asn)
|
|
|
NM_001291867.2(NHS):c.1486C>A (p.Pro496Thr)
|
|
|
NM_001291867.2(NHS):c.1501C>T (p.Arg501Cys)
|
rs770144581
|
|
NM_001291867.2(NHS):c.1514G>A (p.Arg505Gln)
|
|
|
NM_001291867.2(NHS):c.1645C>T (p.Pro549Ser)
|
|
|
NM_001291867.2(NHS):c.1710C>T (p.His570=)
|
|
|
NM_001291867.2(NHS):c.1796A>G (p.Asn599Ser)
|
|
|
NM_001291867.2(NHS):c.1806G>A (p.Thr602=)
|
|
|
NM_001291867.2(NHS):c.1925C>A (p.Pro642His)
|
|
|
NM_001291867.2(NHS):c.1995G>A (p.Ser665=)
|
|
|
NM_001291867.2(NHS):c.207GCC[3] (p.Pro73del)
|
rs10590816
|
|
NM_001291867.2(NHS):c.2096C>T (p.Ala699Val)
|
|
|
NM_001291867.2(NHS):c.2225G>A (p.Arg742His)
|
|
|
NM_001291867.2(NHS):c.2261C>T (p.Thr754Ile)
|
|
|
NM_001291867.2(NHS):c.2448G>A (p.Gly816=)
|
|
|
NM_001291867.2(NHS):c.2592C>T (p.Asn864=)
|
|
|
NM_001291867.2(NHS):c.2682C>T (p.Phe894=)
|
|
|
NM_001291867.2(NHS):c.2688C>T (p.Asn896=)
|
|
|
NM_001291867.2(NHS):c.2720C>T (p.Pro907Leu)
|
|
|
NM_001291867.2(NHS):c.2749C>A (p.Gln917Lys)
|
|
|
NM_001291867.2(NHS):c.2762G>A (p.Gly921Asp)
|
|
|
NM_001291867.2(NHS):c.2789C>T (p.Ser930Leu)
|
|
|
NM_001291867.2(NHS):c.2880T>C (p.Tyr960=)
|
|
|
NM_001291867.2(NHS):c.2910G>A (p.Thr970=)
|
|
|
NM_001291867.2(NHS):c.2932A>G (p.Ile978Val)
|
|
|
NM_001291867.2(NHS):c.3049G>A (p.Gly1017Ser)
|
|
|
NM_001291867.2(NHS):c.3057A>G (p.Ala1019=)
|
rs751373846
|
|
NM_001291867.2(NHS):c.310_345del (p.Pro104_Ala115del)
|
rs797045741
|
|
NM_001291867.2(NHS):c.3132A>G (p.Pro1044=)
|
|
|
NM_001291867.2(NHS):c.3215C>T (p.Thr1072Ile)
|
|
|
NM_001291867.2(NHS):c.3666T>C (p.Thr1222=)
|
|
|
NM_001291867.2(NHS):c.3687C>T (p.Cys1229=)
|
|
|
NM_001291867.2(NHS):c.3828G>C (p.Arg1276Ser)
|
|
|
NM_001291867.2(NHS):c.3890A>G (p.Asp1297Gly)
|
|
|
NM_001291867.2(NHS):c.4030T>C (p.Phe1344Leu)
|
|
|
NM_001291867.2(NHS):c.4128G>C (p.Gln1376His)
|
|
|
NM_001291867.2(NHS):c.4167T>C (p.Ser1389=)
|
rs767452227
|
|
NM_001291867.2(NHS):c.4222+18T>C
|
|
|
NM_001291867.2(NHS):c.4314T>C (p.Pro1438=)
|
|
|
NM_001291867.2(NHS):c.4380T>C (p.Asp1460=)
|
|
|
NM_001291867.2(NHS):c.4428_4430dup (p.Ser1480dup)
|
rs398124609
|
|
NM_001291867.2(NHS):c.4536A>G (p.Thr1512=)
|
|
|
NM_001291867.2(NHS):c.4676G>C (p.Ser1559Thr)
|
|
|
NM_001291867.2(NHS):c.4858C>T (p.Arg1620Trp)
|
|
|
NM_001291867.2(NHS):c.565+17T>C
|
|
|
NM_001291867.2(NHS):c.566-10dup
|
rs5901624
|
|
NM_001291867.2(NHS):c.566-12C>T
|
|
|
NM_001291867.2(NHS):c.566-13_566-12insG
|
|
|
NM_001291867.2(NHS):c.667G>A (p.Val223Met)
|
|
|
NM_001291867.2(NHS):c.687C>T (p.His229=)
|
|
|
NM_001291867.2(NHS):c.819G>A (p.Arg273=)
|
|
|
NM_001291867.2(NHS):c.851C>T (p.Thr284Met)
|
|
|
NM_001291867.2(NHS):c.950T>C (p.Met317Thr)
|
|
|