rs263069746 SNP Detail

Summary

• ID
  rs263069746
• 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
  Chr12:17728120 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              ATAGCATCAG AGGCCAGAAG
  AGGGTGTTGG GTCCCCTGGA ACTGGAGTTA CAGATGGTTG TGAGTCCCCA TGTAGTTTAA
  GAATTAAGCC CAGGTCTTTT GGAAGAACAG TCGGTGCTCT TAACCTCTGA TCTGTCTCTC
  CAGCCCCTTA TTTTATTAGT ATGTATGTAT GTATGTATGT ATGTATGTAT TTATTTATTT
  W
  ATATGCATGA ATGTGTATGA GTGTCTGGAA ACTAAAAATA ATTATAGGTG AGTTCTAGAA
  GCTAAACCCA AGTCTTCTGC AAGAGCAACA AGTATTATTA CCCATTGAGC CATCTCTTCA
  GCCCTGTCCC TTAGCCTTAG TTTACTTTTA AGTGTGTGTG TGTGTGTGTG TGTGTGTGTG
  TGTATCTCTG TCTGTATATG                                            
  
  W = A/T
  

  
  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
ss323926870	CHEV_12_17684925	CHEVERUD	SCREENING_POP	f	SNP	T	A
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs263069746					SNP	T	A