rs47626695 SNP Detail

Summary

• ID
  rs47626695
• Variation Type
  SNP
• Alleles
  C/T

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  ChrX:111861617 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              CAATAATGTA TAACTGAGGG
  GAAGACAAAG TGAAGAATCT GAGAAAATTT TCACAGAATG AGGCAGAGAT AGAATATGCC
  CAACTCTCAG GAGAAAAGCT ATTTAAGTGC AGTGCAGGGA GAGAGTTCAG TTTGTCAATG
  AGTTGGCAAA AAGTCAGTTG GGAGTTAATG TAGTGCTTTG CAGTGGAGTT GAGTTGACTT
  Y
  CTTCATGAGT TCACACAGTT CAGTGCAGGT AGGAAACAGT TGAAGCCAAA GACTAAAAAG
  CCAGAAGATT AGGACAAATT GACATTTGAG GCCAAGCAGA GCAATTCAGT GGAAAGCTGA
  GAGAAGCCAG ATTGAATGAA TTAGCTTGGA GAGGAGTTTG AGCCAGAACA GCTGAGTTGA
  ACCAGCTAGT CCCAGTTCAG                                            
  
  Y = C/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
ss325913371	CHEV_X_110065529	CHEVERUD	SCREENING_POP	f	SNP	T	C
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs47626695					SNP	T	C