rs108879318 SNP Detail

Summary

• ID
  rs108879318
• 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
  Chr4:147167739 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      T TGGAACCAAA CCAGGATGAC AAGAACAAAC ATGCCAAACA
  GGATGGAGAC AAAAAAAGCC CATGAGGCTT CAACACTGAG TGCTACAGTC AACTGGATAC
  G
  ATTTATATAC AGTTTAGGGG GTGATTCAGG ATTCGATAAC AGGTGAGTTG CAAGTTGGGG
  AGGTTGTCTT TTCCAGGCAA GAGCACCCCA AATGCTAGTC 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
ss147934657	ENSMUSSNP3547882	ENSEMBL	ENSEMBL_Sanger	f	SNP	G	G
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J
rs108879318					SNP	G	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:147167739 () rs orientation: forward

Symbol	Name	Function Class
Rr604464	regulatory region 604464	962 bp proximal