rs108859515 SNP Detail

Summary

• ID
  rs108859515
• Variation Type
  SNP
• Alleles
  C

• 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
  Chr7:8446486 (GRCm39)
• SNP Orientation to the Genome
  reverse

• SNP Reference Flanking Sequence

                      T TCTTCTTTCG CCCCGTCTAG ATTCCTCTCT TACAGCTCGA
  GTAGCCTTCT CAGTCGAACC GTTCATGTTG CGAGCTGCTG GCGGCCACAA CATAATATCA
  C
  CATTATTGTT TACTATAGTA AATATTTATT CAAATCTCTG TTTGTCTTTA TAATATCCTT
  TCTCATGCCT ATCTTTGTTT TCTGGGAATT TATGGTTTTA C                    
  
  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	129X1/SvJ
ss148269822	ENSMUSSNP5560922	ENSEMBL	ENSEMBL_Sanger	f	SNP	C
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ
rs108859515					SNP	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr7:8446486 () rs orientation: reverse

Symbol	Name	Function Class
Rr380370	regulatory region 380370	within coordinates