rs45668882 SNP Detail

Summary

• ID
  rs45668882
• Variation Type
  SNP
• Alleles
  A/G

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr3:29121259 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        GGGCCACCAA CTCTCATGAG TGCTGCAGCC AGTTAGGGGC
  AAGGCCAGGT TTCCCACTCT TATGACCTCT GTTCCAGCTC CCTGGCCTGC TGCAGGCAGA
  R
  GGGGGAAAGA GTGGGGAGGG AATTTCTCCT TTGCCCAAAC ATCCCATGAC ATACCAGGGA
  CACGGACAGC TTTCCTGTGC CCACACCATT AAGAGCTGC                       
  
  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	129X1/SvJ	A/J	DBA/2J
ss134720633	ENSMUSSNP2594449	ENSEMBL	ENSEMBL_Sanger	f	SNP	G	G	A
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J
rs45668882					SNP	G	G	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:29121259 () rs orientation: forward

Symbol	Name	Function Class
Rr574657	regulatory region 574657	1503 bp proximal