NM_016335.6(PRODH):c.1292G>A (p.Arg431His)
|
rs2904552
|
0.06735
|
NM_016335.6(PRODH):c.650G>A (p.Arg217His)
|
rs148375080
|
0.00695
|
NM_016335.6(PRODH):c.865T>A (p.Leu289Met)
|
rs137852934
|
0.00464
|
NM_016335.6(PRODH):c.1322T>C (p.Leu441Pro)
|
rs2904551
|
0.00282
|
NM_016335.6(PRODH):c.1217C>T (p.Pro406Leu)
|
rs3970555
|
0.00149
|
NM_016335.6(PRODH):c.1363G>T (p.Ala455Ser)
|
rs1807467
|
0.00112
|
NM_016335.6(PRODH):c.578G>A (p.Gly193Asp)
|
rs199907923
|
0.00029
|
NM_016335.6(PRODH):c.1729C>T (p.Arg577Trp)
|
rs184218784
|
0.00020
|
NM_016335.6(PRODH):c.319A>G (p.Lys107Glu)
|
rs140129512
|
0.00014
|
NM_016335.6(PRODH):c.392G>A (p.Arg131Gln)
|
rs145456430
|
0.00007
|
NM_016335.6(PRODH):c.1093G>A (p.Val365Ile)
|
rs768237039
|
0.00006
|
NM_016335.6(PRODH):c.1295G>A (p.Arg432His)
|
rs143011525
|
0.00006
|
NM_016335.6(PRODH):c.1181C>T (p.Thr394Met)
|
rs777930066
|
0.00005
|
NM_016335.6(PRODH):c.853A>G (p.Ser285Gly)
|
rs199829422
|
0.00005
|
NM_016335.6(PRODH):c.1652A>C (p.Tyr551Ser)
|
rs142346005
|
0.00003
|
NM_016335.6(PRODH):c.338T>A (p.Phe113Tyr)
|
rs372030860
|
0.00003
|
NM_016335.6(PRODH):c.391C>T (p.Arg131Trp)
|
rs753625227
|
0.00003
|
NM_016335.6(PRODH):c.80G>T (p.Arg27Leu)
|
rs1411529753
|
0.00003
|
NM_016335.6(PRODH):c.1174C>T (p.Arg392Cys)
|
rs1336190354
|
0.00002
|
NM_016335.6(PRODH):c.1763G>A (p.Arg588Lys)
|
rs1239323884
|
0.00002
|
NM_016335.6(PRODH):c.1006G>A (p.Ala336Thr)
|
rs1160517835
|
0.00001
|
NM_016335.6(PRODH):c.1294C>T (p.Arg432Cys)
|
rs376682221
|
0.00001
|
NM_016335.6(PRODH):c.131C>G (p.Thr44Arg)
|
rs562183461
|
0.00001
|
NC_000022.10:g.(?_18899287)_(18925066_?)dup
|
|
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NC_000022.10:g.(?_18900668)_(18906024_?)dup
|
|
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NC_000022.10:g.(?_18900668)_(18923820_?)dup
|
|
|
NC_000022.10:g.(?_18900688)_(18904521_?)dup
|
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|
NC_000022.10:g.(?_18900688)_(18923800_?)dup
|
|
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NC_000022.10:g.(?_18906944)_(18923800_?)dup
|
|
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NM_016335.6(PRODH):c.1003A>G (p.Asn335Asp)
|
rs1044791075
|
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NM_016335.6(PRODH):c.1012-3C>T
|
rs371062452
|
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NM_016335.6(PRODH):c.1036T>G (p.Ser346Ala)
|
rs2081951548
|
|
NM_016335.6(PRODH):c.1049A>G (p.Glu350Gly)
|
|
|
NM_016335.6(PRODH):c.106G>A (p.Ala36Thr)
|
|
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NM_016335.6(PRODH):c.1085G>A (p.Arg362Gln)
|
|
|
NM_016335.6(PRODH):c.1091A>G (p.Asp364Gly)
|
rs1057524390
|
|
NM_016335.6(PRODH):c.1133T>A (p.Met378Lys)
|
rs752953633
|
|
NM_016335.6(PRODH):c.1163C>T (p.Pro388Leu)
|
rs147233639
|
|
NM_016335.6(PRODH):c.118G>C (p.Gly40Arg)
|
rs780423887
|
|
NM_016335.6(PRODH):c.1190T>G (p.Met397Arg)
|
|
|
NM_016335.6(PRODH):c.1238A>C (p.Gln413Pro)
|
|
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NM_016335.6(PRODH):c.1251+6C>T
|
|
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NM_016335.6(PRODH):c.1278C>A (p.Asp426Glu)
|
|
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NM_016335.6(PRODH):c.128C>T (p.Ala43Val)
|
|
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NM_016335.6(PRODH):c.1301G>A (p.Gly434Asp)
|
|
|
NM_016335.6(PRODH):c.130_156del (p.Thr44_Ala52del)
|
rs949036081
|
|
NM_016335.6(PRODH):c.1310T>C (p.Phe437Ser)
|
|
|
NM_016335.6(PRODH):c.1328G>A (p.Arg443Gln)
|
|
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NM_016335.6(PRODH):c.1350G>T (p.Glu450Asp)
|
|
|
NM_016335.6(PRODH):c.1362_1363delinsAT (p.Ala455Ser)
|
rs2081943034
|
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NM_016335.6(PRODH):c.1373G>A (p.Gly458Asp)
|
|
|
NM_016335.6(PRODH):c.1390A>C (p.Asn464His)
|
rs2146209436
|
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NM_016335.6(PRODH):c.1397C>A (p.Thr466Lys)
|
rs2870984
|
|
NM_016335.6(PRODH):c.1402G>A (p.Glu468Lys)
|
rs372618210
|
|
NM_016335.6(PRODH):c.1418T>C (p.Met473Thr)
|
rs1555890224
|
|
NM_016335.6(PRODH):c.1427+4C>T
|
|
|
NM_016335.6(PRODH):c.1471G>T (p.Ala491Ser)
|
rs1241975657
|
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NM_016335.6(PRODH):c.1497T>A (p.Asn499Lys)
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|
|
NM_016335.6(PRODH):c.1515_1516inv (p.Ala506Thr)
|
|
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NM_016335.6(PRODH):c.151C>T (p.Pro51Ser)
|
|
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NM_016335.6(PRODH):c.1527-3C>T
|
rs2146205858
|
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NM_016335.6(PRODH):c.152C>T (p.Pro51Leu)
|
|
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NM_016335.6(PRODH):c.1531G>A (p.Glu511Lys)
|
|
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NM_016335.6(PRODH):c.1544T>G (p.Leu515Arg)
|
|
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NM_016335.6(PRODH):c.1558C>T (p.His520Tyr)
|
|
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NM_016335.6(PRODH):c.1576C>T (p.Gln526Ter)
|
rs372187772
|
|
NM_016335.6(PRODH):c.1612C>A (p.Leu538Met)
|
|
|
NM_016335.6(PRODH):c.1633G>A (p.Val545Met)
|
|
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NM_016335.6(PRODH):c.1660G>A (p.Val554Met)
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|
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NM_016335.6(PRODH):c.1748G>T (p.Trp583Leu)
|
|
|
NM_016335.6(PRODH):c.1772G>A (p.Arg591Gln)
|
rs779412444
|
|
NM_016335.6(PRODH):c.1786T>C (p.Phe596Leu)
|
|
|
NM_016335.6(PRODH):c.1791T>G (p.His597Gln)
|
|
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NM_016335.6(PRODH):c.1792C>T (p.Arg598Cys)
|
|
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NM_016335.6(PRODH):c.1793G>A (p.Arg598His)
|
|
|
NM_016335.6(PRODH):c.1803G>A (p.Ter601=)
|
rs1183388799
|
|
NM_016335.6(PRODH):c.187C>T (p.Arg63Cys)
|
|
|
NM_016335.6(PRODH):c.193C>T (p.Arg65Trp)
|
|
|
NM_016335.6(PRODH):c.1A>G (p.Met1Val)
|
rs1036292619
|
|
NM_016335.6(PRODH):c.223C>A (p.Leu75Met)
|
rs1391433654
|
|
NM_016335.6(PRODH):c.22C>T (p.Pro8Ser)
|
rs944412642
|
|
NM_016335.6(PRODH):c.237G>C (p.Leu79Phe)
|
rs2008733
|
|
NM_016335.6(PRODH):c.268G>A (p.Glu90Lys)
|
rs1023813331
|
|
NM_016335.6(PRODH):c.273G>A (p.Gln91=)
|
rs2146223897
|
|
NM_016335.6(PRODH):c.296T>G (p.Leu99Arg)
|
|
|
NM_016335.6(PRODH):c.298C>G (p.Leu100Val)
|
|
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NM_016335.6(PRODH):c.305A>G (p.Gln102Arg)
|
|
|
NM_016335.6(PRODH):c.309G>T (p.Arg103Ser)
|
|
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NM_016335.6(PRODH):c.350T>C (p.Phe117Ser)
|
|
|
NM_016335.6(PRODH):c.358G>A (p.Gly120Arg)
|
rs979499476
|
|
NM_016335.6(PRODH):c.383C>T (p.Pro128Leu)
|
rs2146219914
|
|
NM_016335.6(PRODH):c.418G>A (p.Ala140Thr)
|
|
|
NM_016335.6(PRODH):c.41T>C (p.Ile14Thr)
|
|
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NM_016335.6(PRODH):c.427G>T (p.Asp143Tyr)
|
|
|
NM_016335.6(PRODH):c.482+6G>A
|
rs571651683
|
|
NM_016335.6(PRODH):c.485C>A (p.Ser162Tyr)
|
|
|
NM_016335.6(PRODH):c.531_532delinsTA (p.Asp178Asn)
|
|
|
NM_016335.6(PRODH):c.583A>G (p.Ile195Val)
|
|
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NM_016335.6(PRODH):c.593G>T (p.Arg198Leu)
|
|
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NM_016335.6(PRODH):c.610A>G (p.Asn204Asp)
|
|
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NM_016335.6(PRODH):c.611A>G (p.Asn204Ser)
|
|
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NM_016335.6(PRODH):c.649C>T (p.Arg217Cys)
|
|
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NM_016335.6(PRODH):c.679G>A (p.Asp227Asn)
|
|
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NM_016335.6(PRODH):c.697A>C (p.Ile233Leu)
|
|
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NM_016335.6(PRODH):c.721C>T (p.Pro241Ser)
|
|
|
NM_016335.6(PRODH):c.733C>T (p.Leu245=)
|
|
|
NM_016335.6(PRODH):c.767G>T (p.Cys256Phe)
|
|
|
NM_016335.6(PRODH):c.803C>T (p.Ala268Val)
|
rs375358521
|
|
NM_016335.6(PRODH):c.829C>A (p.Leu277Met)
|
rs143408578
|
|
NM_016335.6(PRODH):c.850-10A>G
|
|
|
NM_016335.6(PRODH):c.880A>G (p.Arg294Gly)
|
rs2081960374
|
|
NM_016335.6(PRODH):c.925T>C (p.Ser309Pro)
|
|
|
NM_016335.6(PRODH):c.929+3G>A
|
|
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NM_016335.6(PRODH):c.92C>T (p.Ala31Val)
|
|
|
NM_016335.6(PRODH):c.933_934inv (p.Met312Val)
|
|
|
NM_016335.6(PRODH):c.934A>G (p.Met312Val)
|
|
|
NM_016335.6(PRODH):c.964G>A (p.Asp322Asn)
|
|
|