rs222579818 SNP Detail

Summary

• ID
  rs222579818
• 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
  Chr12:17729159 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              ACACAAGACA TAAAAGACTG
  GGTCCCTGTC ACCTAGAGGT GACATTTTAA TCTTAGGTTT CCTACCTTTG GGCTACTGCT
  TTTTTGTTTC TTTGTTTTTT TCTTTCTTTT TCATTAAAAT TAACTTACTC AAATTATAAC
  AAACACTGTA AATAGCCCAT TAGTGTATGA CTTTCTGCAT GTATGTGTGT GTGCACAAGT
  R
  CATGTAAAAC CTAAAAGGTC AGCTACATTG TTGTTCTTCC TCAATTGCCA TGCACCTTGT
  TGAGATGGGA TCTCTTACCA GTAGGCCTGG AGCTCACCAA TCATGTGACT GGCTGGCTGA
  CCAGCAAGCC CCGGACATGG ACCTCCCTAG CCCTGGGGTA AGAGACACGC ACTACCATGC
  CTTGCTTTTT ATGCAGGTTC                                            
  
  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
ss323926885	CHEV_12_17685964	CHEVERUD	SCREENING_POP	f	SNP	A	G
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs222579818					SNP	A	G