rs264647033 SNP Detail

Summary

• ID
  rs264647033
• Variation Type
  SNP
• Alleles
  A/G

• Created in dbSNP Build
  137
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr13:114658973 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                    gaacaaagg gcccccaatg gatgagctag
  agaaagtacc caaggagcta aaggggtctg caaccctata ggtggaacaa caatatgaac
  taaccagtac ccccagagct gtgtctctag ctgcatatgt agcagaagat ggcctagttg
  R
  ccatcaatgg gaagagtggc cctttggtat tgcaaacttt atatgcctca gtacagggga
  atgctagggc caagaagtgg gagtgggtgg gtaggggagt cgggggtagg gtatagcgga
  attttgggat agcatttgaa atgtaaatga                                 
  
  R = A/G
  

  
  Note: Sequence in lower case indicates low-complexity or repetitive sequence

  ---

SNP Assays
and
SNP Consensus

Strain alleles of submitted assays, and consensus values for this SNP

Assay ID	Submitter SNP ID	Submitter Handle	Population	ss orientation	Variation Type	LG/J	SM/J
ss324534042	CHEV_13_115312645	CHEVERUD	SCREENING_POP	f	SNP	G	A
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs264647033					SNP	G	A