rs108925220 SNP Detail

Summary

• ID
  rs108925220
• Variation Type
  SNP
• Alleles
  A/C

• Created in dbSNP Build
  132
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr2:167226326 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        TGCAATCCAC ATCAGGCCAC AAGTTATAAG TTTTTTTTTC
  CCCCGTTTTT CCAGACAGGG TCTCTCTGTA TAGCCCTGGC TGTCCTGGAC TTTGCTCTGT
  M
  GAGCAGGCTG GCCTCTCTCT GCATCCCCAG TGCTAGGATT GAAGGTGGGT GCTACTACAG
  CCTGGCTCAC AATAAGATTG AAAACGAGCA CCATTGTCA                       
  
  M = A/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	129X1/SvJ	A/J	DBA/2J
ss148262651	ENSMUSSNP3848313	ENSEMBL	ENSEMBL_Sanger	f	SNP	A	A	C
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J
rs108925220					SNP	A	A	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:167226326 () rs orientation: forward

Symbol	Name	Function Class
Rr397506	regulatory region 397506	389 bp downstream
Tssr21804	transcription start site region 21804	333 bp downstream
Tssr21805	transcription start site region 21805	310 bp downstream
Tssr27773	transcription start site region 27773	834 bp upstream