rs234989612 SNP Detail

Summary

• ID
  rs234989612
• Variation Type
  SNP
• Alleles
  A/G

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

Genome Location and Flanking Sequence

• Location
  Chr9:97934692 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              CGGATGTTTC CTTACCCTCA
  CATGATAACT AGACATTACA ATGATAACTA GATTTTACCA TATAGGTATG TACACATACC
  TCTATGTGTG TCTTCGGCAC AAATACATGG CATGTATTAT TCATTTCTGA TTATTAATCT
  TTTACTAAGT ACCATTTTGA ATTGTGGAGT GTTCTAGGTT GTTCTTGTGT GACTGAGACT
  R
  AGGAAAAGAT GCTCTTCTCT GCATTTAAAC TCAGCCTCAT GCTGAGGACT CGATTAATAA
  GCAGGACTCA GAAAAAGAGA AGAGAAAGGA GTAAGGATAG GAAGAAGTGG AAGCAAGAAA
  GGATTGCTTG CAGATTCTAT GACGCACATG CATGTAGAAA CTATCTGAAG ACAGGTGTTA
  GGACCAGGAA GAGCTCGAGT                                            
  
  R = A/G
  

  
  Note: Sequence in lower case indicates low-complexity or repetitive sequence

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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	LG/J	SM/J
ss323125299	CHEV_9_97953058	CHEVERUD	SCREENING_POP	f	SNP	A	G
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs234989612					SNP	A	G