rs47567868 SNP Detail

Summary

• ID
  rs47567868
• Variation Type
  SNP
• Alleles
  C

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

Genome Location and Flanking Sequence

• Location
  Chr2:127928704 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        CGTGATTCTC AGTGGACCTG GTTGGTTTTA TTTAAACTTC
  TCTGACAGTC TCGATTCTTT CAGCAGATTT ATGAGACTTG GCCAAATTCC ATGTCTCCGA
  C
  TTATACTTTT TAATTAAGAC AAAGAATCCC ACACCTTCCT GGTTGGCCCC ATCCTCCCTA
  TCGTCACCAG CGGGAATGCC ATACAAATCA GACCACTTG                       
  
  C = C
  

  
  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	DBA/2J
ss147551037	ENSMUSSNP2607568	ENSEMBL	ENSEMBL_Sanger	f	SNP	C
SNP Consensus Information
SNP					Consensus Type	DBA/2J
rs47567868					SNP	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:127928704 () rs orientation: forward

Symbol	Name	Function Class
Acoxl	acyl-Coenzyme A oxidase-like	Intron
Gm74890	predicted gene, 74890	190 bp upstream
Rr564640	regulatory region 564640	1705 bp distal
Rr564641	regulatory region 564641	164 bp proximal
Rr564642	regulatory region 564642	1060 bp proximal