rs108897444 SNP Detail

Summary

• ID
  rs108897444
• Variation Type
  SNP
• Alleles
  G

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

Genome Location and Flanking Sequence

• Location
  ChrX:134935835 (GRCm39)
• SNP Orientation to the Genome
  reverse

• SNP Reference Flanking Sequence

                      T TCAGCCTTCC CTAATTCAAT AACAGGGGCC AGCTGTTTCT
  GTCCATTGGG TGGGTGCAAA TATCTGGATC TGACTCTTCC AGCTGCTTGT TGGGTCTTCT
  G
  GAGTGCAGTC ATGCTAGGTC CCTTTTTGTG AGTGCTTTAC AGCCTCAGCA ATAGTGTCAG
  GCCTTGGGAC CTCCCCTTGA GCTGGATCCC ACTTTGAGCC T                    
  
  G = 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
ss145588198	ENSMUSSNP7059810	ENSEMBL	ENSEMBL_Sanger	f	SNP	G	G	G
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J
rs108897444					SNP	G	G	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: ChrX:134935835 () rs orientation: reverse

Symbol	Name	Function Class
Arxes1	adipocyte-related X-chromosome expressed sequence 1	140 bp downstream
Rr693722	regulatory region 693722	1709 bp distal