rs47916760 SNP Detail

Summary

• ID
  rs47916760
• Variation Type
  SNP
• Alleles
  A/G

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  132
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr10:7017172 (GRCm39)
• SNP Orientation to the Genome
  reverse

• SNP Reference Flanking Sequence

                      T TGTGAACATC TCTGCTGATG GTGGAAAACA AGCTGTGGAA
  TTAGCCCCTG CTATTTTTAA TGCTATGCAA AAGCAGGGGA CTAGAGGATG ACCCCACACA
  R
  GGAGGCGCTG AGGAAGTGCC TTCTGGAAAT AGAAATGTAC TTACTGCAAA ACTAAGAGAT
  TTGCTTCTGG TCAAAATGTT CGGTGTCTTA ATTAGTGTTC T                    
  
  R = A/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	A/J	MSM/Ms
ss146641810	ENSMUSSNP764926	ENSEMBL	ENSEMBL_Sanger	f	SNP	A	G
SNP Consensus Information
SNP					Consensus Type	A/J	MSM/Ms
rs47916760					SNP	A	G