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Gene polymorphism

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446:(GWAS). There have been a number of studies looking into various polymorphisms of asthma-associated genes and how those polymorphisms interact with the carrier's environment. One example is the gene CD14, which is known to have a polymorphism that is associated with increased amounts of CD14 protein as well as reduced levels of IgE serum. A study was conducted on 624 children looking at their IgE serum levels as it related to the polymorphism in CD14. The study found that IgE serum levels differed in children with the C allele in the CD14/-260 gene based on the type of allergens they regularly exposed to. Children who were in regular contact with house pets showed higher serum levels of IgE while children who were regularly exposed to stable animals showed lower serum levels of IgE. Continued research into gene-environment interactions may lead to more specialized treatment plans based on an individual's surroundings. 402:. Asp312Asn and Lys751Gln are the two common polymorphisms of XPD that result in a change in a single amino acid. This variation in Asn and Gln alleles has been related to individuals having a reduced DNA repair efficiency. Several studies have been conducted to see if this diminished capacity to repair DNA is related to an increased risk of lung cancer. These studies examined the XPD gene in lung cancer patients of varying age, gender, race, and 424:
is becoming increasingly important to understand the specific mutations involved in the individual's cancer, such as needed to select specific molecular targets such as mutations in various receptors, but also understanding the polymorphisms they inherited which play important roles in diagnosis,
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Gene polymorphisms can occur in any region of the genome. The majority of polymorphisms are silent, meaning they do not alter the function or expression of a gene. Some polymorphisms are visible. For example, in dogs the E locus can have any of five different alleles, known as E, E, E, E, and e.
406:. The studies provided mixed results, from concluding individuals who are homozygous for the Asn allele or homozygous for the Gln allele had an increased risk of developing lung cancer, to finding no statistical significance between smokers who have either allele polymorphism and their 1424:
Misra, R Rita; Ratnasinghe, Duminda; Tangrea, Joseph A; Virtamo, Jarmo; Andersen, Mark R; Barrett, Michael; Taylor, Philip R; Albanes, Demetrius (2003). "Polymorphisms in the DNA repair genes XPD, XRCC1, XRCC3, and APE/ref-1, and the risk of lung cancer amongmale smokers in Finland".
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Asthma is an inflammatory disease of the lungs and more than 100 loci have been identified as contributing to the development and severity of the condition. By using the traditional linkage analysis, these asthma correlated genes were able to be identified in small quantities using
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A polymorphic variant of a gene can lead to the abnormal expression or to the production of an abnormal form of the protein; this abnormality may cause or be associated with disease. For example, a polymorphic variant of the gene encoding the enzyme
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Baldini, M.; Lohman, I. C.; Halonen, M.; Erickson, R. P.; Holt, P. G.; Martinez, F. D. (May 1999). "A Polymorphism* in the 5' flanking region of the CD14 gene is associated with circulating soluble CD14 levels and with total serum immunoglobulin E".
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rather than polymorphisms. However, since polymorphisms may occur at low allele frequency, this is not a reliable way to tell new mutations from polymorphisms. A mutation is a change to an inherited genetic sequence.
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at the gene's nucleotide 8590 position encodes a CYP4A11 protein that substitutes phenylalanine with serine at the protein's amino acid position 434. This variant protein has reduced enzyme activity in metabolizing
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Eder, Waltraud; Klimecki, Walt; Yu, Lizhi; von Mutius, Erika; Riedler, Josef; Braun-Fahrländer, Charlotte; Nowak, Dennis; Martinez, Fernando D.; Allergy And Endotoxin Alex Study Team (September 2005).
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within a population. In addition to having more than one allele at a specific locus, each allele must also occur in the population at a rate of at least 1% to generally be considered polymorphic.
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Bodmer, J. G.; Marsh, S. G. E.; Albert, E. D.; Bodmer, W. F.; Bontrop, R. E.; Dupont, B.; Erlich, H. A.; Hansen, J. A.; Mach, B. (1999-04-01). "Nomenclature for factors of the HLA system, 1998".
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nearly all mutations are not passed on to subsequent generations. A mutation may, or may not, be passed on to off-spring (e.g. if is a mutation that happens in some replicating cells
178:, which can be subsequently passed on to future generations, and it is very helpful to be clear when discussing mutations whether it is a somatic mutation or germline mutation. 38: 319:
Many different human disease result from polymorphisms. Polymorphisms also play significant role as risk factors for development of disease. Finally, polymorphisms in
236:(i.e. silent or resulting in some change in function or change in fitness). Polymorphisms are also classified based on whether the change is in the sequence of the 363: 310:
are repeats of 1-6 base pairs of DNA sequence. Microsatellites are commonly used as a molecular markers especially for identifying the relationship between alleles
1269:"Polymorphisms in XPD Gene Could Predict Clinical Outcome of Platinum-Based Chemotherapy for Non-Small Cell Lung Cancer Patients: A Meta-Analysis of 24 Studies" 501: 414: 398:. XPD works by cutting and removing segments of DNA that have been damaged due to things such as cigarette smoking and inhalation of other environmental 330:, proteins involved in drug transport (whether into the body, into protected areas of the body like the brain, or secreted out) as well as in specific 164: 279:
are a single nucleotide changes that happen in the genome in a particular location. The single nucleotide polymorphism is the most common form of
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sequence is repeated (both of these are common in parts of DNA that don't directly code for a protein, as are SNPs, but can have major effects on
1462:"ITPA, TPMT, and NUDT15 Genetic Polymorphisms Predict 6-Mercaptopurine Toxicity in Middle Eastern Children With Acute Lymphoblastic Leukemia" 811:"Discovery and verification of functional single nucleotide polymorphisms in regulatory genomic regions: Current and developing technologies" 550: 1151: 1014:
Mills RE, Pittard WS, Mullaney JM, Farooq U, Creasy TH, Mahurkar AA, Kemeza DM, Strassler DS, Ponting CP, Webber C, Devine SE (2011).
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can they spread into a population. Polymorphisms are classified based on what happens at the level of the individual mutation in the
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Moradveisi, Borhan; Muwakkit, Samar; Zamani, Fatemeh; Ghaderi, Ebrahim; Mohammadi, Ebrahim; Zgheib, Nathalie K. (2019-08-27).
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Qin, Qin; Zhang, Chi; Yang, Xi; Zhu, Hongcheng; Yang, Baixia; Cai, Jing; Cheng, Hongyan; Ma, Jianxin; Lu, Jing (2013-11-15).
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of human MHC class I and II genes, and it has been estimated that there are 200 variants at the HLA-B HLA-DRB1 loci alone.
90:. A study has shown that humans bearing this variant in one or both of their CYP4A11 genes have an increased incidence of 1112: 809:
Chorley, Brian N.; Wang, Xuting; Campbell, Michelle R.; Pittman, Gary S.; Noureddine, Maher A.; Bell, Douglas A. (2008).
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proteins alter the effect of various drugs. This is a rapidly evolving area of drug safety research. Resources such as
109:(MHC) are in fact the most polymorphic genes known. MHC molecules are involved in the immune system and interact with 512: 410:. Research continues to be conducted to determine the relationship between XPD polymorphisms and lung cancer risk. 106: 256:
to amplify the sequence of a gene. Once amplified, polymorphisms and mutations in the sequence can be detected by
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A rule of thumb that is sometimes used is to classify genetic variants that occur below 1% allele frequency as
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can also cause polymorphism by inserting themselves in new locations. For example, repetitive elements of the
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of the gene, which can occur at sites that are typically upstream and adjacent to the gene, but not always.
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Liang, Gang; Xing, Deyin; Miao, Xiaoping; Tan, Wen; Yu, Chunyuan; Lu, Wenfu; Lin, Dongxin (2003-07-10).
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where toxicity largely depends on polymorphisms in multiple different genes involved in its metabolism.
407: 1220:"The XPD variant alleles are associated with increased aromatic DNA adduct level and lung cancer risk" 253: 205: 61:
Varying combinations of these alleles contribute to the pigmentation and patterns seen in dog coats.
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Polymorphisms can be identified in the laboratory using a variety of methods. Many methods employ
1621:"Opposite effects of CD 14/-260 on serum IgE levels in children raised in different environments" 99: 1377:"Sequence variations in the DNA repair gene XPD and risk of lung cancer in a Chinese population" 462: 220:. All genetic polymorphisms start out as a mutation, but only if they are germline and are not 926:
Sadee, W; Wang, D; Papp, AC; Pinsonneault, JK; Smith, RM; Moyer, RA; Johnson, AD (March 2011).
347: 558: 387: 367: 331: 1280: 293: 209: 8: 145: 121: 1284: 1016:"Natural genetic variation caused by small insertions and deletions in the human genome" 1549: 1520: 1496: 1461: 1311: 1268: 1089: 1064: 1040: 1015: 960: 927: 900: 867: 843: 810: 783: 748: 724: 689: 608: 583: 1438: 1169: 1650: 1642: 1598: 1590: 1554: 1501: 1483: 1442: 1406: 1398: 1357: 1316: 1298: 1249: 1241: 1094: 1045: 1000: 965: 947: 905: 887: 848: 830: 788: 770: 729: 711: 656: 648: 644: 613: 421: 280: 160: 1632: 1582: 1544: 1534: 1491: 1473: 1434: 1388: 1347: 1306: 1288: 1231: 1084: 1076: 1035: 1027: 955: 939: 895: 879: 838: 822: 778: 760: 719: 701: 640: 603: 595: 463:"Genetic polymorphism - Biology-Online Dictionary | Biology-Online Dictionary" 430: 375: 216:). Polymorphisms which result in a change in fitness are the grist for the mill of 149: 79: 54: 1293: 928:"Pharmacogenomics of the RNA World: Structural RNA Polymorphisms in Drug Therapy" 747:
Karki, Roshan; Pandya, Deep; Elston, Robert C.; Ferlini, Cristiano (2015-07-15).
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Karki, Roshan; Pandya, Deep; Elston, Robert C.; Ferlini, Cristiano (2015-07-15).
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Occurrence in an interbreeding population of two or more discontinuous genotypes
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mutations there isn't a change in fitness, and the pressures responsible for
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Polymorphisms have been discovered in multiple XPD exons. XPD refers to "
297: 260:, either directly or after screening for variation with a method such as 229: 1539: 749:"Defining "mutation" and "polymorphism" in the era of personal genomics" 690:"Defining "mutation" and "polymorphism" in the era of personal genomics" 192:
equilibrium have no impact on the accumulation of silent polymorphisms
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A polymorphism can be any sequence difference. Examples include:
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For example, a mutation may occur in a skin cell as a result of
1521:"Genetic polymorphisms and associated susceptibility to asthma" 1459: 417: 110: 95: 50: 1423: 1336:"ERCC2 /XPD gene polymorphisms and lung cancer: a HuGE review" 584:"20-HETE and blood pressure regulation: clinical implications" 167:
which is not properly repaired before the skin cell undergoes
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This is quite distinct from a mutation which occurs during
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American Journal of Respiratory Cell and Molecular Biology
1065:"Small insertions and deletions (INDELs) in human genomes" 1062: 1013: 808: 925: 582:
Wu CC, Gupta T, Garcia V, Ding Y, Schwartzman ML (2014).
1618: 746: 687: 675:"Genetic Polymorphism and How It Lasts over Generations" 364:
International Nucleotide Sequence Database Collaboration
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Research, Center for Drug Evaluation and (2024-02-02).
630: 1518: 1152:"Table of Pharmacogenomic Biomarkers in Drug Labeling" 1113:"Difference Between Minisatellite and Microsatellite" 1063:
Mullaney JM, Mills RE, Pittard WS, Devine SE (2010).
1201:, National Center for Biotechnology Information (US) 551:"E-Locus (Recessive Yellow, Melanistic Mask Allele)" 141:
In unicellular organisms, there isn't a distinction.
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consist of insertions or deletions of bases in DNA.
1001:"What are single nucleotide polymorphisms (SNPs)?" 502:"Technologic Issues in GWAS and Follow-up Studies" 128:Differences between gene polymorphism and mutation 581: 156:, none of the off-spring will bear the mutation. 1665: 1374: 481:National Human Genome Research Institute (NHGRI) 262:single strand conformation polymorphism analysis 144:In multi-cellular organisms which replicate via 41:Genes which control hair colour are polymorphic. 1333: 1266: 425:prognosis, and treatment, such as treatment of 1625:The Journal of Allergy and Clinical Immunology 577: 575: 356:Kyoto Encyclopedia of Genes and Genomes (KEGG) 1512: 1327: 304:families cause polymorphisms in human genome. 1056: 1007: 1519:March ME, Sleiman PM, Hakonarson H (2013). 1195:"GenBank: The Nucleotide Sequence Database" 572: 232:), and what effect the mutation has on the 204:of one or more nucleotides, changes in the 49:is said to be polymorphic if more than one 804: 802: 1636: 1548: 1538: 1526:International Journal of General Medicine 1495: 1477: 1392: 1351: 1310: 1292: 1235: 1088: 1039: 959: 899: 842: 782: 764: 723: 705: 607: 287:Small-scale insertions/deletions (Indels) 1192: 1149: 921: 919: 872:Journal of Psychiatry & Neuroscience 314: 292:Polymorphic repetitive elements. Active 36: 799: 499: 120:Some polymorphism may be maintained by 113:. There are more than 32,000 different 105:Most notably, the genes coding for the 14: 1666: 986:Genetics, Mutations, and Polymorphisms 932:Clinical Pharmacology and Therapeutics 865: 277:Single nucleotide polymorphisms (SNPs) 1614: 1612: 916: 982: 240:protein or in the regulation of the 1217: 24: 1609: 633:European Journal of Immunogenetics 25: 1690: 866:Albert, Paul R. (November 2011). 681: 477:"Genetic Testing Report-Glossary" 247: 82:to the blood pressure-regulating 1340:American Journal of Epidemiology 645:10.1046/j.1365-2370.1999.00159.x 228:(or RNA sequence in the case of 198:variation in a single nucleotide 196:. Most often, a polymorphism is 107:major histocompatibility complex 1565: 1453: 1417: 1381:International Journal of Cancer 1368: 1260: 1211: 1186: 1162: 1143: 1119: 1105: 993: 976: 859: 740: 500:Chanock, Stephen (2017-05-22). 444:genome-wide association studies 88:20-hydroxyeicosatetraenoic acid 1334:Benhamou S, Sarasin A (2005). 1193:Mizrachi, Ilene (2007-08-22), 667: 624: 543: 529: 493: 469: 455: 390:group D" and is involved in a 381: 218:evolution by natural selection 13: 1: 1439:10.1016/s0304-3835(02)00638-9 449: 408:susceptibility to lung cancer 1294:10.1371/journal.pone.0079864 600:10.1097/CRD.0b013e3182961659 7: 827:10.1016/j.mrrev.2008.05.001 10: 1695: 1638:10.1016/j.jaci.2005.05.003 537:"Dog Coat Colour Genetics" 362:, and other parts of the 29: 1466:Frontiers in Pharmacology 1218:Hou, S.-M. (2002-04-01). 766:10.1186/s12920-015-0115-z 707:10.1186/s12920-015-0115-z 436: 1587:10.1165/ajrcmb.20.5.3494 1479:10.3389/fphar.2019.00916 1069:Human Molecular Genetics 267: 30:For other concepts, see 1237:10.1093/carcin/23.4.599 1170:"Genomics and Medicine" 1127:"Polygenic Risk Scores" 366:have become crucial in 200:(SNP), but also can be 100:coronary artery disease 1679:Polymorphism (biology) 394:mechanism used during 348:DNA Data Bank of Japan 42: 1032:10.1101/gr.115907.110 944:10.1038/clpt.2010.314 555:www.animalgenetics.us 388:xeroderma pigmentosum 368:Personalized medicine 332:cell surface receptor 315:Clinical significance 294:transposable elements 202:insertion or deletion 53:occupies that gene's 40: 18:Genetic polymorphisms 989:. Landes Bioscience. 983:Bull, Laura (2013). 753:BMC Medical Genomics 694:BMC Medical Genomics 588:Cardiology in Review 415:Peronalized medicine 413:As a cornerstone of 1540:10.2147/IJGM.S28156 1285:2013PLoSO...879864Q 146:sexual reproduction 122:balancing selection 1353:10.1093/aje/kwi018 1199:The NCBI Handbook 1081:10.1093/hmg/ddq400 884:10.1503/jpn.110137 43: 1394:10.1002/ijc.11136 815:Mutation Research 465:. September 2020. 422:Sequence analysis 281:genetic variation 161:ultraviolet light 150:that are not part 16:(Redirected from 1686: 1659: 1658: 1640: 1616: 1607: 1606: 1569: 1563: 1562: 1552: 1542: 1516: 1510: 1509: 1499: 1481: 1457: 1451: 1450: 1421: 1415: 1414: 1396: 1372: 1366: 1365: 1355: 1331: 1325: 1324: 1314: 1296: 1264: 1258: 1257: 1239: 1215: 1209: 1208: 1207: 1206: 1190: 1184: 1183: 1181: 1180: 1166: 1160: 1159: 1147: 1141: 1140: 1138: 1137: 1123: 1117: 1116: 1109: 1103: 1102: 1092: 1060: 1054: 1053: 1043: 1011: 1005: 1004: 997: 991: 990: 980: 974: 973: 963: 923: 914: 913: 903: 863: 857: 856: 846: 821:(1–2): 147–157. 806: 797: 796: 786: 768: 744: 738: 737: 727: 709: 685: 679: 678: 671: 665: 664: 628: 622: 621: 611: 579: 570: 569: 567: 566: 557:. Archived from 547: 541: 540: 533: 527: 526: 524: 523: 517: 511:. Archived from 506: 497: 491: 490: 488: 487: 473: 467: 466: 459: 431:6-mercaptopurine 376:pharmacogenomics 80:arachidonic acid 21: 1694: 1693: 1689: 1688: 1687: 1685: 1684: 1683: 1664: 1663: 1662: 1617: 1610: 1570: 1566: 1517: 1513: 1458: 1454: 1422: 1418: 1373: 1369: 1332: 1328: 1265: 1261: 1216: 1212: 1204: 1202: 1191: 1187: 1178: 1176: 1168: 1167: 1163: 1148: 1144: 1135: 1133: 1125: 1124: 1120: 1111: 1110: 1106: 1061: 1057: 1020:Genome Research 1012: 1008: 999: 998: 994: 981: 977: 924: 917: 864: 860: 807: 800: 745: 741: 686: 682: 673: 672: 668: 639:(2–3): 81–116. 629: 625: 580: 573: 564: 562: 549: 548: 544: 535: 534: 530: 521: 519: 515: 504: 498: 494: 485: 483: 475: 474: 470: 461: 460: 456: 452: 439: 396:DNA replication 384: 325:cytochrome p450 321:drug metabolism 317: 308:Microsatellites 270: 250: 214:gene expression 206:number of times 184:In the case of 163:resulting in a 130: 35: 28: 23: 22: 15: 12: 11: 5: 1692: 1682: 1681: 1676: 1661: 1660: 1631:(3): 601–607. 1608: 1581:(5): 976–983. 1564: 1511: 1452: 1433:(2): 171–178. 1427:Cancer Letters 1416: 1387:(5): 669–673. 1367: 1326: 1279:(11): e79864. 1259: 1230:(4): 599–603. 1224:Carcinogenesis 1210: 1185: 1174:www.genome.gov 1161: 1142: 1131:www.genome.gov 1118: 1104: 1075:(R2): R131–6. 1055: 1006: 992: 975: 938:(3): 355–365. 915: 878:(6): 363–365. 858: 798: 739: 680: 666: 623: 571: 542: 528: 492: 468: 453: 451: 448: 438: 435: 383: 380: 372:bioinformatics 316: 313: 312: 311: 305: 290: 284: 269: 266: 258:DNA sequencing 249: 248:Identification 246: 190:Hardy-Weinberg 182: 181: 180: 179: 172: 165:thiamine dimer 142: 129: 126: 26: 9: 6: 4: 3: 2: 1691: 1680: 1677: 1675: 1672: 1671: 1669: 1656: 1652: 1648: 1644: 1639: 1634: 1630: 1626: 1622: 1615: 1613: 1604: 1600: 1596: 1592: 1588: 1584: 1580: 1576: 1568: 1560: 1556: 1551: 1546: 1541: 1536: 1532: 1528: 1527: 1522: 1515: 1507: 1503: 1498: 1493: 1489: 1485: 1480: 1475: 1471: 1467: 1463: 1456: 1448: 1444: 1440: 1436: 1432: 1428: 1420: 1412: 1408: 1404: 1400: 1395: 1390: 1386: 1382: 1378: 1371: 1363: 1359: 1354: 1349: 1345: 1341: 1337: 1330: 1322: 1318: 1313: 1308: 1304: 1300: 1295: 1290: 1286: 1282: 1278: 1274: 1270: 1263: 1255: 1251: 1247: 1243: 1238: 1233: 1229: 1225: 1221: 1214: 1200: 1196: 1189: 1175: 1171: 1165: 1157: 1153: 1146: 1132: 1128: 1122: 1114: 1108: 1100: 1096: 1091: 1086: 1082: 1078: 1074: 1070: 1066: 1059: 1051: 1047: 1042: 1037: 1033: 1029: 1025: 1021: 1017: 1010: 1002: 996: 988: 987: 979: 971: 967: 962: 957: 953: 949: 945: 941: 937: 933: 929: 922: 920: 911: 907: 902: 897: 893: 889: 885: 881: 877: 873: 869: 862: 854: 850: 845: 840: 836: 832: 828: 824: 820: 816: 812: 805: 803: 794: 790: 785: 780: 776: 772: 767: 762: 758: 754: 750: 743: 735: 731: 726: 721: 717: 713: 708: 703: 699: 695: 691: 684: 676: 670: 662: 658: 654: 650: 646: 642: 638: 634: 627: 619: 615: 610: 605: 601: 597: 593: 589: 585: 578: 576: 561:on 2017-10-30 560: 556: 552: 546: 538: 532: 518:on 2018-08-22 514: 510: 503: 496: 482: 478: 472: 464: 458: 454: 447: 445: 434: 432: 428: 423: 419: 416: 411: 409: 405: 401: 397: 393: 389: 379: 377: 373: 369: 365: 361: 357: 353: 349: 345: 341: 337: 333: 329: 326: 322: 309: 306: 303: 299: 295: 291: 288: 285: 282: 278: 275: 274: 273: 265: 263: 259: 255: 245: 243: 239: 235: 231: 227: 223: 219: 215: 211: 207: 203: 199: 195: 191: 187: 177: 173: 170: 166: 162: 158: 157: 155: 151: 147: 143: 140: 139: 138: 135: 125: 123: 118: 116: 112: 108: 103: 101: 97: 93: 89: 85: 81: 76: 72: 68: 62: 58: 56: 52: 48: 39: 33: 19: 1628: 1624: 1578: 1574: 1567: 1530: 1524: 1514: 1469: 1465: 1455: 1430: 1426: 1419: 1384: 1380: 1370: 1343: 1339: 1329: 1276: 1272: 1262: 1227: 1223: 1213: 1203:, retrieved 1198: 1188: 1177:. Retrieved 1173: 1164: 1155: 1145: 1134:. Retrieved 1130: 1121: 1107: 1072: 1068: 1058: 1026:(6): 830–9. 1023: 1019: 1009: 995: 985: 978: 935: 931: 875: 871: 861: 818: 814: 756: 752: 742: 697: 693: 683: 669: 636: 632: 626: 591: 587: 563:. Retrieved 559:the original 554: 545: 531: 520:. Retrieved 513:the original 508: 495: 484:. Retrieved 480: 471: 457: 440: 412: 385: 318: 271: 251: 226:DNA sequence 183: 171:and divides. 131: 119: 104: 92:hypertension 63: 59: 44: 32:Polymorphism 1346:(1): 1–14. 594:(1): 1–12. 400:carcinogens 382:Lung cancer 230:RNA viruses 208:a short or 94:, ischemic 69:, in which 1668:Categories 1533:: 253–65. 1205:2024-02-17 1179:2024-02-17 1136:2024-02-17 565:2017-11-08 522:2017-11-30 509:Genome.gov 486:2017-11-08 450:References 404:pack-years 392:DNA repair 328:isoenzymes 242:expression 84:eicosanoid 1647:0091-6749 1595:1044-1549 1488:1663-9812 1403:1097-0215 1303:1932-6203 1246:0143-3334 952:0009-9236 892:1180-4882 835:0027-5107 775:1755-8794 716:1755-8794 653:1365-2370 238:resulting 234:phenotype 194:over time 134:mutations 73:replaces 71:thymidine 1655:16159630 1603:10226067 1559:23637549 1506:31507415 1447:12618330 1411:12740916 1362:15615908 1321:24260311 1273:PLOS ONE 1254:11960912 1099:20858594 1050:21460062 970:21289622 910:22011561 853:18565787 793:26173390 734:26173390 661:10331156 618:23584425 427:leukemia 352:DrugBank 154:germline 75:cytosine 1550:3636804 1497:6718715 1472:: 916. 1312:3829883 1281:Bibcode 1090:2953750 1041:3106316 961:3251919 901:3201989 844:2676583 784:4502642 725:4502642 609:4292790 418:cancers 360:GenBank 344:Ensembl 323:, esp. 176:meiosis 169:mitosis 152:of the 115:alleles 111:T-cells 67:CYP4A11 1653:  1645:  1601:  1593:  1557:  1547:  1504:  1494:  1486:  1445:  1409:  1401:  1360:  1319:  1309:  1301:  1252:  1244:  1097:  1087:  1048:  1038:  968:  958:  950:  908:  898:  890:  851:  841:  833:  791:  781:  773:  759:: 37. 732:  722:  714:  700:: 37. 659:  651:  616:  606:  437:Asthma 374:, and 336:HapMap 222:lethal 210:longer 186:silent 98:, and 96:stroke 51:allele 1674:Genes 516:(PDF) 505:(PDF) 429:with 340:DbSNP 302:LINE1 268:Types 55:locus 1651:PMID 1643:ISSN 1599:PMID 1591:ISSN 1555:PMID 1502:PMID 1484:ISSN 1443:PMID 1407:PMID 1399:ISSN 1358:PMID 1317:PMID 1299:ISSN 1250:PMID 1242:ISSN 1095:PMID 1046:PMID 966:PMID 948:ISSN 906:PMID 888:ISSN 849:PMID 831:ISSN 789:PMID 771:ISSN 730:PMID 712:ISSN 657:PMID 649:ISSN 614:PMID 300:and 47:gene 1633:doi 1629:116 1583:doi 1545:PMC 1535:doi 1492:PMC 1474:doi 1435:doi 1431:191 1389:doi 1385:105 1348:doi 1344:161 1307:PMC 1289:doi 1232:doi 1156:FDA 1085:PMC 1077:doi 1036:PMC 1028:doi 956:PMC 940:doi 896:PMC 880:doi 839:PMC 823:doi 819:659 779:PMC 761:doi 720:PMC 702:doi 641:doi 604:PMC 596:doi 298:Alu 254:PCR 1670:: 1649:. 1641:. 1627:. 1623:. 1611:^ 1597:. 1589:. 1579:20 1577:. 1553:. 1543:. 1529:. 1523:. 1500:. 1490:. 1482:. 1470:10 1468:. 1464:. 1441:. 1429:. 1405:. 1397:. 1383:. 1379:. 1356:. 1342:. 1338:. 1315:. 1305:. 1297:. 1287:. 1275:. 1271:. 1248:. 1240:. 1228:23 1226:. 1222:. 1197:, 1172:. 1154:. 1129:. 1093:. 1083:. 1073:19 1071:. 1067:. 1044:. 1034:. 1024:21 1022:. 1018:. 964:. 954:. 946:. 936:89 934:. 930:. 918:^ 904:. 894:. 886:. 876:36 874:. 870:. 847:. 837:. 829:. 817:. 813:. 801:^ 787:. 777:. 769:. 755:. 751:. 728:. 718:. 710:. 696:. 692:. 655:. 647:. 637:26 635:. 612:. 602:. 592:22 590:. 586:. 574:^ 553:. 507:. 479:. 420:, 378:. 370:, 358:, 354:, 350:, 346:, 338:, 264:. 124:. 102:. 86:, 45:A 1657:. 1635:: 1605:. 1585:: 1561:. 1537:: 1531:6 1508:. 1476:: 1449:. 1437:: 1413:. 1391:: 1364:. 1350:: 1323:. 1291:: 1283:: 1277:8 1256:. 1234:: 1182:. 1158:. 1139:. 1115:. 1101:. 1079:: 1052:. 1030:: 1003:. 972:. 942:: 912:. 882:: 855:. 825:: 795:. 763:: 757:8 736:. 704:: 698:8 677:. 663:. 643:: 620:. 598:: 568:. 539:. 525:. 489:. 342:, 283:. 34:. 20:)

Index

Genetic polymorphisms
Polymorphism

gene
allele
locus
CYP4A11
thymidine
cytosine
arachidonic acid
eicosanoid
20-hydroxyeicosatetraenoic acid
hypertension
stroke
coronary artery disease
major histocompatibility complex
T-cells
alleles
balancing selection
mutations
sexual reproduction
that are not part
germline
ultraviolet light
thiamine dimer
mitosis
meiosis
silent
Hardy-Weinberg
over time

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