The Single Nucleotide Polymorphism Database (dbSNP) is a free public archive for genetic variation within and across different species developed and hosted...
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Single-nucleotide polymorphism (redirect from SNP mutation)
United States National Library of Medicine. 2014. NCBI dbSNP build 142 for human. "[DBSNP-announce] DBSNP Human Build 142 (GRCh38 and GRCh37.p13)". Archived...
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Type=String,Description="Ancestral Allele"> ##INFO=<ID=DB,Number=0,Type=Flag,Description="dbSNP membership, build 129"> ##INFO=<ID=H2,Number=0,Type=Flag...
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annotation (SNP annotation) is the process of predicting the effect or function of an individual SNP using SNP annotation tools. In SNP annotation the...
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mutation at position 342 (dbSNP: rs28929474), while PiS is caused by a glutamic acid to valine mutation at position 264 (dbSNP: rs17580). Other rarer forms...
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(SNPs) in public databases such as dbSNP. More common recessive phenotypes would be more likely to have disease-causing variants reported in dbSNP. For...
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0090. PMC 3125548. PMID 21348634. dbSNP Data Statistics. National Center for Biotechnology Information (US). 2005. "dbSNP Summary". Tarvo, Alex. "Tutorial...
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known as genomic selection. Crop-specific arrays find use in agriculture. "dbSNP Summary". www.ncbi.nlm.nih.gov. Retrieved 4 October 2017. The 1000 Genomes...
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population. 1. Introduce the reference of a SNP of interest, as an example: rs429358, in a database (dbSNP or other). 2. Find MAF/MinorAlleleCount link...
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inactive as of May 2024 (link) CS1 maint: location missing publisher (link) "DBSNP Home Page". National Center for Biotechnology Information, U.S. National...
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; Sirotkin, Karl; Ward, Minghong; Sherry, Stephen T. (1 January 2000). "dbSNP: a database of single nucleotide polymorphisms". Nucleic Acids Research...
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Inheritance in Man, the Molecular Modeling Database (3D protein structures), dbSNP (a database of single-nucleotide polymorphisms), the Reference Sequence...
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are documented in specific databases. The variants could be obtained from dbSNP, 1000 Genomes Project, or user-supplied list. Additional information could...
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Ensembl project integrates HapMap data with other genetic information from dbSNP. PLINK – whole genome association analysis toolset, which can calculate...
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doi:10.1182/blood-2017-08-803080. PMID 29438961. "rs397514502 RefSNP Report - dbSNP - NCBI". www.ncbi.nlm.nih.gov. Duk, Maria; Reinhold, Bruce B; Reinhold...
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gastrocardiac symptoms Stomatal resistance (rs), of leaves rs, prefix of a DbSNP record ID number e.g. rs206437 Respiratory syncytial virus, a species of...
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of base-pairs than the SNPs and indels. As of 2017[update], the Single Nucleotide Polymorphism Database (dbSNP), which lists SNP and other variants, listed...
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Factor V Leiden (category SNPs on chromosome 1)
referred to as F5. Mutation of this gene—a single nucleotide polymorphism (SNP) is located in exon 10. As a missense substitution of amino acid R to amino...
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1371/journal.pone.0042752. PMC 3418284. PMID 22912732. "rs16891982 RefSNP Report - dbSNP - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2022-10-02. Adhikari, Kaustubh...
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doi:10.1038/gim.2012.165. PMID 23288205. S2CID 12461781. "rs1801133". dbSNP. National Library of Medicine. Retrieved 26 April 2023. Schneider JA, Rees...
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ISSN 0036-8075. PMC 2884988. PMID 19679812. "rs121912617 RefSNP Report - dbSNP - NCBI". dbSNP. "rs121912617 - SNPedia". www.snpedia.com. Retrieved 2022-10-14...
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entered on 16 August 2014 into the SNP database dbSNP at the National Center for Biotechnology Information as reference SNP cluster report rs767290651. R-Z18...
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sequences, the sequence multi-alignment of the HuRef assembly, Ensembl and dbSNP annotations, HuRef variants, and the underlying variant evidence and functional...
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Chemistry, Vol. 243, No. 5, Issue of March 10, pages 980–991. "rs33948057". dbSNP. National Center for Biotechnology Information. Retrieved 7 February 2014...
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rapidly evolving area of drug safety research. Resources such as HapMap, DbSNP,Ensembl, DNA Data Bank of Japan, DrugBank, Kyoto Encyclopedia of Genes and...
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Rs1801133 (category SNPs on chromosome 1)
C677T or rs1801133 is a genetic variation—a single nucleotide polymorphism (SNP)—in the MTHFR gene. Among Americans the frequency of T-homozygosity ranges...
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of 2017[update], the Single Nucleotide Polymorphism Database (dbSNP), which lists SNP and other variants, listed a total of 324 million variants found...
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5-HTTLPR (category SNPs on chromosome 17)
In connection with the region are two single nucleotide polymorphisms (SNP): rs25531 and rs25532. One study published in 2000 found 14 allelic variants...
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International HapMap Project (redirect from SNP Consortium)
were submitted to the public dbSNP database. As a result, by August 2006, the database included more than ten million SNPs, and more than 40% of them were...
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genomes. The use of a reference single nucleotide polymorphism (SNP) map, such as dbSNP, can be used to further improve the number of variants for storage...
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