rs263625935 SNP Detail

Summary

• ID
  rs263625935
• 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
  Chr13:114658246 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              AGTCTCCAGC CTGTTGTGGG
  AGGAAATATA GGCTTGCAAA GAAAATATGT GCAATAATAA GCTATGACAA CTGTCTACTT
  AACAACATTG TCTTATCTGC ACTTGCTTAT CAGTCATCAC AGAGAAAGTC TCATGGAATT
  TCATCTCTAA TAGAAAATCC ACACCACATT GAAAGTTGCT CCCTCTCCCT CTCTCTCTGC
  R
  TTTTTTCAAG ACAAGGCTTT CCCATGTAAG AGCCATGGCT GTTCTGGAAC TTGCTTGGTA
  GACCACACTG GCCTCATTCA TGTTTTCTTT TTAAGCCTAT TGTCTTGTCC GTAAATGTGA
  CGTTCTACAT CTTTCAGTGG AAACTGTTGC TTATATGATG GCTCTAAAGG TTAATTAGTA
  GTTCAATATT GTTGTTTTAC                                            
  
  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
ss324534039	CHEV_13_115311918	CHEVERUD	SCREENING_POP	f	SNP	G	A
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs263625935					SNP	G	A