rs108715732 SNP Detail

Summary

• ID
  rs108715732
• Variation Type
  SNP
• Alleles
  G

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

Genome Location and Flanking Sequence

• Location
  Chr3:94445982 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              AAATAAAGAT AGCCAAGACC
  TACCAGGCTG AAAAGAGCAA GAAAAAGAAG GAAGATGAAG ATGAGGAGGA GGATGAAGAG
  AATTAGGTAG AAGAGGAAGA GGAGGAAAGA AGACAAGGAT GAAGAAGATG ATGATGATGA
  TGAATAAGTT GGTTCTAGGG CAGTTTTTTT TCTGTCTATA AAGCATTCAA ACCCCCTCCC
  G
  TACATAACTC ATTCCTTTTA AAGACAAAAG TTGAAATGGG AAAAAAAAAA AAAAAGTCAA
  GACCTAGAGA ACAAATGAGT AAGATGGTGG AGTAACTGAT TATAGCAATA ATTACACTGT
  TAATAATTTA ACACTCCAAA TAAAGACTAA CATTACCAAG TTACATGAAG AAACCCAGTT
  AAAAGCTATC TATAAAAAGC                                            
  
  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
ss135505888	ENSMUSSNP1335782	ENSEMBL	ENSEMBL_Sanger	f	SNP	G
SNP Consensus Information
SNP					Consensus Type	DBA/2J
rs108715732					SNP	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:94445982 () rs orientation: forward

Symbol	Name	Function Class
Gm43774	predicted gene 43774	1187 bp upstream
Rr375397	regulatory region 375397	1221 bp downstream
Snx27	sorting nexin family member 27	Intron