rs237967855 SNP Detail

Summary

• ID
  rs237967855
• Variation Type
  SNP
• Alleles
  C/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
  Chr9:97933771 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              CCTGCATCCG TGAAGACAAC
  AAGCACACTG CTAAGCCTGT GATCACGAGG GGCACGTGAT CCCAGGCTGT AGTTAAGTTG
  TCGGGTAATA CTGATGAACA ATGCCCGAAC GTGGCATTAG GGACCCACTT AGAGACGTTT
  TTAAGGGTAA CGATCAGCAA AACTACAACT AACTCTGCAT GGTTCAAGAA AAGATGTAGC
  Y
  ATGTCTGTGT CTCCATGTAT GTAAGGGACA GAAAAAAAAA AAGGGGAGAG GGGGAAAATA
  AAAGAAAATA GTTTCGTGCA AGCGGGAGAA ATAGAACATC AAGTGTCCAT CAAACCAGCC
  TTGACACTTG TCACTTACAG AACTGAGAAG CATAATAGCG ATTTAAATAA AATTTATCAA
  TATAAAAACA CAGTCCCTGA                                            
  
  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
ss323125296	CHEV_9_97952137	CHEVERUD	SCREENING_POP	f	SNP	C	T
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs237967855					SNP	C	T