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Resource Name
dbSNP151
RRID:SCR_028814 RRID Copied      
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dbSNP151 (RRID:SCR_028814)
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Resource Information

URL: https://genome.ucsc.edu/cgi-bin/hgTrackUi?db=hg38&g=snp151

Proper Citation: dbSNP151 (RRID:SCR_028814)

Description: Database containing common germline alterations. dbSNP build 151 contains a subset of common germline variants (such as single nucleotide polymorphisms) defined by a minor allele frequency (MAF) of 1% or greater in major population groups.Database is used as a reference for various applications, such as measuring non-synonymous mutations in tumor mutation burden calculations.

Resource Type: data or information resource, database

Keywords: common germline alterations, subset of common germline variants, minor allele frequency,

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dbSNP

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