rs46189455 SNP Detail

Summary

• ID
  rs46189455
• Variation Type
  SNP
• Alleles
  A/T

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  132
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr3:65843671 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      A CATGGTGGCT CACAACCATC TGTAATGGGA TCTGATGCCC
  TCTCCTGCTG TGTCTGAAGA CAGCAATGGT GTACTCATAT ACAGAAAATA AATAAATCTT
  W
  AAAAAAAAGA AAGTATCACT TTTGCTGATG CATAATATAC CTTCTGTTAT CATGATCTTC
  AGGGATGTTT TCCTAAAACT CTCAAATCTC TTTCTTCATT G                    
  
  W = A/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	DBA/2J	MSM/Ms
ss135254264	ENSMUSSNP671227	ENSEMBL	ENSEMBL_Sanger	f	SNP	A	A	T
SNP Consensus Information
SNP					Consensus Type	A/J	DBA/2J	MSM/Ms
rs46189455					SNP	A	A	T