rs224268899 SNP Detail

Summary

• ID
  rs224268899
• 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
  Chr9:97933355 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TGTGAACACA TAAAGTGAAA
  GGAATAATGA AAATTACAAG AGAAATCAGT GATAAAAAGG GAACAAAAGA TTAATAATAC
  TGAAGACGGT GCTTTGAAAA TATTGAACTA GGCAAAACTC TGCCACAATT AATCTATAAA
  AAGGGAATAA AAAACACATT AGCACTCCTA GGAATGAAAA AGAAGTACAA AACCAAGTGT
  R
  CTGAAGATAA TTAAAAGATA ATAAGCGGAT TTTATGAATA ATGTATGCTA ATAAAATTTT
  AAACTCTGAT GAAACAAATA AATCCTAAGA AAACTGAAGA TCACCGTCAG ATGTTGAAAT
  TATTTAACGT ATTTGGCAAG CCTGGAAATC ATTCTGGTGT AAAGGAAAGT GACGAGAAAT
  GGCAAGCACA GCAGACAACA                                            
  
  R = A/G
  

  
  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
ss323125293	CHEV_9_97951721	CHEVERUD	SCREENING_POP	f	SNP	A	G
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs224268899					SNP	A	G