rs107926673 SNP Detail

Summary

• ID
  rs107926673
• 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
  Chr6:32666752 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      G CTATACTTAC GGGTACCCTG TTCCCCAGCA GAAGAGTTCT
  GAATTCACGC AGTTGAATCC TTCTCAACAG TCTGTGTTGT GGGAACACTT CATTACCACC
  G
  TTCCCCAGCT GAAGAGTTCT GAATTCACGC AGTTGAGTCC TTCTCAACAG TCTGTTTTGC
  GGGAACCTTT ATGACCGTGA CCCGCAGTTC TGGTTCCGGA A                    
  
  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	DBA/2J
ss133101367	ENSMUSSNP6625207	ENSEMBL	ENSEMBL_Sanger	f	SNP	G
SNP Consensus Information
SNP					Consensus Type	DBA/2J
rs107926673					SNP	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr6:32666752 () rs orientation: forward

Symbol	Name	Function Class
Rr379152	regulatory region 379152	48 bp upstream