rs107668535 SNP Detail

Summary

• ID
  rs107668535
• 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
  Chr1:85321338 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      T AAGAGTTGCT TTAGTCATGG TGTCTCTTCA CAGCAATAAA
  ACCCCAACAG AAGAATCATC TGAGAAAAGA ACTTCTTCAG CTGTGTATTC TAGGTTGGGG
  G
  CATTATAGTT AGACCCAGCC ACTGTGGCTT CCTGGGTATG AGAGCAGAGA AAGTAAGAGG
  AGCATGAACA TGCACTTGTT AATGCATTGC TCTCTGCAGG C                    
  
  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
ss144854871	ENSMUSSNP1809034	ENSEMBL	ENSEMBL_Sanger	f	SNP	G
SNP Consensus Information
SNP					Consensus Type	DBA/2J
rs107668535					SNP	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr1:85321338 () rs orientation: forward

Symbol	Name	Function Class
Gm7281	predicted gene 7281	1531 bp upstream
Gm16025	predicted gene 16025	1002 bp downstream
Rr414358	regulatory region 414358	1197 bp distal