rs52319882 SNP Detail

Summary

• ID
  rs52319882
• Variation Type
  SNP
• Alleles
  T

• Created in dbSNP Build
  128
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr2:153793373 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TTATCCATCT ATCAATCTAC
  CCATCCTCCT CCAATACTCT GGGACAGTTT GAGGATTTGA GATGTGGCAG TATGAACCAT
  ACATTTCACA GCTTCTCATA AACATGAGCT ATTTAAAACA AAACAACACA ACAGCAACAA
  CAACAACAAC AAAAACAACA ACAACATCAC TACCCAAAAC ATGGGAATCT GTAATTCTTC
  T
  AAGAAAAAAG TGTCCACTTA GGTTCAGGGC AGCTAGCATT CTTGCAGAGT TATAACATGT
  GACCAGGGCC CTGCCTTGAT AGTGCAACCA TGCAGGAGGC AATGACTTTG CTTGATCTGC
  TGCATTGGTT CCATGGTCTC TCTCTCTCTC TCTCTCTCTC TCTCTCTCTC TCTCTCTCTC
  TCTCTTTCTC CCCCATCCCT                                            
  
  T = T
  

  
  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	A/J
ss148011151	ENSMUSSNP5114648	ENSEMBL	ENSEMBL_Sanger	f	SNP	T
SNP Consensus Information
SNP					Consensus Type	A/J
rs52319882					SNP	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:153793373 () rs orientation: forward

Symbol	Name	Function Class
Bpifb4	BPI fold containing family B, member 4	Intron
Rr567759	regulatory region 567759	1411 bp proximal
Rr567760	regulatory region 567760	1619 bp proximal