NM_006070.6(TFG):c.1006C>T (p.Pro336Ser)
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rs371681149 |
NM_006070.6(TFG):c.1014T>G (p.Asn338Lys)
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rs1553704923 |
NM_006070.6(TFG):c.1030G>A (p.Ala344Thr)
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rs1576389587 |
NM_006070.6(TFG):c.1036C>T (p.Gln346Ter)
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rs1576389617 |
NM_006070.6(TFG):c.1048G>A (p.Ala350Thr)
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rs543542721 |
NM_006070.6(TFG):c.1060C>G (p.Pro354Ala)
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rs111356679 |
NM_006070.6(TFG):c.1070A>G (p.Tyr357Cys)
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rs1375662436 |
NM_006070.6(TFG):c.1087T>G (p.Phe363Val)
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NM_006070.6(TFG):c.1090A>C (p.Thr364Pro)
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rs6772054 |
NM_006070.6(TFG):c.1094C>T (p.Ser365Leu)
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rs1288104441 |
NM_006070.6(TFG):c.1116C>T (p.Thr372=)
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rs1576389880 |
NM_006070.6(TFG):c.1123C>G (p.Pro375Ala)
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rs1234073129 |
NM_006070.6(TFG):c.1133C>T (p.Pro378Leu)
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NM_006070.6(TFG):c.1145C>T (p.Ala382Val)
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rs138185005 |
NM_006070.6(TFG):c.1146G>A (p.Ala382=)
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rs761808737 |
NM_006070.6(TFG):c.1153C>T (p.Arg385Cys)
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NM_006070.6(TFG):c.1154G>A (p.Arg385His)
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NM_006070.6(TFG):c.1157C>T (p.Pro386Leu)
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rs766049461 |
NM_006070.6(TFG):c.1165G>C (p.Gly389Arg)
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rs1576390105 |
NM_006070.6(TFG):c.1172G>T (p.Gly391Val)
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NM_006070.6(TFG):c.1199G>A (p.Arg400Gln)
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rs963151000 |
NM_006070.6(TFG):c.1199G>C (p.Arg400Pro)
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NM_006070.6(TFG):c.185-10T>A
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rs79631225 |
NM_006070.6(TFG):c.185-9A>T
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rs778438842 |
NM_006070.6(TFG):c.196A>G (p.Ile66Val)
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NM_006070.6(TFG):c.237G>T (p.Gln79His)
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rs1173009495 |
NM_006070.6(TFG):c.256C>G (p.Leu86Val)
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NM_006070.6(TFG):c.258G>T (p.Leu86=)
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rs150620449 |
NM_006070.6(TFG):c.268G>A (p.Val90Ile)
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NM_006070.6(TFG):c.286C>T (p.Pro96Ser)
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NM_006070.6(TFG):c.290T>A (p.Leu97His)
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rs1576366321 |
NM_006070.6(TFG):c.302A>G (p.Gln101Arg)
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rs1576366326 |
NM_006070.6(TFG):c.309A>G (p.Lys103=)
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rs369508900 |
NM_006070.6(TFG):c.310T>C (p.Tyr104His)
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rs775608477 |
NM_006070.6(TFG):c.316C>T (p.Arg106Cys)
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rs587777175 |
NM_006070.6(TFG):c.391C>T (p.Pro131Ser)
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rs770053266 |
NM_006070.6(TFG):c.395C>A (p.Ser132Tyr)
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NM_006070.6(TFG):c.409G>C (p.Glu137Gln)
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NM_006070.6(TFG):c.415+7C>G
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rs149927288 |
NM_006070.6(TFG):c.416-9T>C
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rs115896544 |
NM_006070.6(TFG):c.457T>G (p.Ser153Ala)
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rs140466338 |
NM_006070.6(TFG):c.458C>T (p.Ser153Phe)
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rs775354552 |
NM_006070.6(TFG):c.464A>G (p.Lys155Arg)
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NM_006070.6(TFG):c.467A>G (p.Gln156Arg)
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NM_006070.6(TFG):c.482T>C (p.Met161Thr)
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rs766899074 |
NM_006070.6(TFG):c.483G>A (p.Met161Ile)
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rs750964585 |
NM_006070.6(TFG):c.484G>A (p.Ala162Thr)
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NM_006070.6(TFG):c.544A>C (p.Met182Leu)
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NM_006070.6(TFG):c.545T>C (p.Met182Thr)
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rs199724547 |
NM_006070.6(TFG):c.552G>A (p.Ala184=)
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rs35648279 |
NM_006070.6(TFG):c.567T>A (p.Asp189Glu)
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NM_006070.6(TFG):c.57G>A (p.Glu19=)
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rs1576353054 |
NM_006070.6(TFG):c.594T>G (p.Ala198=)
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rs12562 |
NM_006070.6(TFG):c.608G>A (p.Arg203His)
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NM_006070.6(TFG):c.621C>T (p.Pro207=)
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rs141786985 |
NM_006070.6(TFG):c.663C>A (p.Gly221=)
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rs140669729 |
NM_006070.6(TFG):c.663C>T (p.Gly221=)
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rs140669729 |
NM_006070.6(TFG):c.664G>A (p.Val222Ile)
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NM_006070.6(TFG):c.672A>C (p.Pro224=)
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rs141412018 |
NM_006070.6(TFG):c.68G>A (p.Arg23Gln)
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rs774808090 |
NM_006070.6(TFG):c.716T>C (p.Ile239Thr)
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rs146004809 |
NM_006070.6(TFG):c.722-8G>T
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rs41272979 |
NM_006070.6(TFG):c.740A>G (p.Tyr247Cys)
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rs1559723912 |
NM_006070.6(TFG):c.741C>T (p.Tyr247=)
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rs1576379547 |
NM_006070.6(TFG):c.743A>G (p.Gln248Arg)
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rs1576379554 |
NM_006070.6(TFG):c.754G>A (p.Gly252Ser)
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rs561904697 |
NM_006070.6(TFG):c.771G>A (p.Gln257=)
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rs374006808 |
NM_006070.6(TFG):c.774G>A (p.Pro258=)
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rs1367793822 |
NM_006070.6(TFG):c.792G>T (p.Gln264His)
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rs1576379647 |
NM_006070.6(TFG):c.806G>T (p.Gly269Val)
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rs587777789 |
NM_006070.6(TFG):c.826T>C (p.Tyr276His)
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rs1559726842 |
NM_006070.6(TFG):c.852A>C (p.Gln284His)
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rs1559726965 |
NM_006070.6(TFG):c.854C>T (p.Pro285Leu)
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rs207482230 |
NM_006070.6(TFG):c.870A>G (p.Gly290=)
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NM_006070.6(TFG):c.882A>C (p.Gln294His)
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rs751393611 |
NM_006070.6(TFG):c.898C>A (p.Pro300Thr)
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NM_006070.6(TFG):c.898C>T (p.Pro300Ser)
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rs1210008384 |
NM_006070.6(TFG):c.908C>T (p.Ala303Val)
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rs1576389064 |
NM_006070.6(TFG):c.943C>T (p.Pro315Ser)
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rs1553704852 |
NM_006070.6(TFG):c.944C>T (p.Pro315Leu)
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rs753375115 |
NM_006070.6(TFG):c.945G>A (p.Pro315=)
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rs61736338 |
NM_006070.6(TFG):c.976G>T (p.Ala326Ser)
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NM_006070.6(TFG):c.97T>C (p.Tyr33His)
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NM_006070.6(TFG):c.980A>G (p.Gln327Arg)
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rs1431898500 |
NM_006070.6(TFG):c.988A>G (p.Thr330Ala)
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rs145835282 |
NM_006070.6(TFG):c.98A>G (p.Tyr33Cys)
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rs763523148 |
Single allele
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