rs235570799 SNP Detail

Summary

• ID
  rs235570799
• Variation Type
  SNP
• Alleles
  A/C

• 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
  Chr9:119182814 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              AAAGTTCTAA TCTGATTATA
  ATCCCAGCAC TTAGGAGGCT AAGGCAGGAA GATCAATCGC TGTGAGTTTG AGGTCTACAT
  AATGCTAGGC TAGTGTGGTC TGAAGAATAA GACATTATCT ACCCCTGAAA GAGGTAGGGA
  GAGATGGCTC AGTGGGTGAT AGTGGGTTAT TTTCCTGTAT GTTTTCCTTT TCCGTGTCAT
  M
  TCAGTCTATA AGTTACAAGT TATAAGCCAT AGAAAGTAGA CGGCAATGTA AATATAATCA
  CCCCGTAACT GTAACCACCA GTTTCTGAGT CCCAGTGATC TTCATGGTAG CACAGGGGTA
  TGTCTTTCCA GACTTTTCCT TCACGTGTGT GGATGTCCTA GCTTCGAATG TGCACAGAAG
  GAGGCAAGCA GACCCCAAGG                                            
  
  M = A/C
  

  
  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
ss323218984	CHEV_9_119262866	CHEVERUD	SCREENING_POP	f	SNP	A	C
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs235570799					SNP	A	C