rs212981992 SNP Detail

Summary

• ID
  rs212981992
• 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
  Chr9:97933164 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TACTACATTG CCATATTGAA
  TATAATAAAT ACACTATATA TTTATTAATT CAATTATTAA TAAACTAGTG CTTAGAAAGT
  ATAGCCTAAT TTGTGTATTA GAAAATATTT CTTAATTTAT ATTTAACGGG TTAAGCACTC
  TACATAAAAA GTAAAAAAAA AAAAGTAAAA AATGAAATAC TATAATAGCG CTGTGAACAC
  R
  TAAAGTGAAA GGAATAATGA AAATTACAAG AGAAATCAGT GATAAAAAGG GAACAAAAGA
  TTAATAATAC TGAAGACGGT GCTTTGAAAA TATTGAACTA GGCAAAACTC TGCCACAATT
  AATCTATAAA AAGGGAATAA AAAACACATT AGCACTCCTA GGAATGAAAA AGAAGTACAA
  AACCAAGTGT GCTGAAGATA                                            
  
  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	LG/J	SM/J
ss323125292	CHEV_9_97951530	CHEVERUD	SCREENING_POP	f	SNP	G	A
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs212981992					SNP	G	A