rs262972295 SNP Detail

Summary

• ID
  rs262972295
• Variation Type
  SNP
• Alleles
  A/T

• 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
  Chr9:97931410 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              CTATTGGAAC CTGCTGAAGT
  CTGCCCTCCA GGATATAAGG AAAGGCTACA ATCAGAGTGT TATGAAGTCT TAGAACTCAG
  AAGGTTCTAG GGGAAACTGC TGGCTGATAA TGAAGCCATA GGTTGGAAAG ACTGTTCCCT
  GTGGTTCAAG GCCAACGCAT GAGCTGGAAA TTGGATGGAG ATGCTATCAC TTGCTAAAAA
  W
  TTTTAGGAGC CCACTGAATT CACTGTAAAG GGAGACACTG AAGATGTAAC TGCCAAGAAA
  GTAGAGTCTT AAAAGTAACA TTTCAATAGG AGAATACAAA AAGAAAGGAA ATAAATAGAG
  TCTTCCCCCA GCAAAGAAAG AAAGTGACAG ACAACCTAGA GAACAGAGAA CTGGAACGGA
  AAACGGAGTT AGCATCTAGA                                            
  
  W = A/T
  

  
  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
ss323125286	CHEV_9_97949776	CHEVERUD	SCREENING_POP	f	SNP	T	A
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs262972295					SNP	T	A