rs223912080 SNP Detail

Summary

• ID
  rs223912080
• Variation Type
  SNP
• Alleles
  G/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
  Chr12:17729686 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              GCCTAGGGTG CATTTTCTTG
  ATTGATTGAT GCCTGACTGA TTGATTGATT GATGACTGGG TGATTGGTGT GGGAGGGCCA
  AGCCACCCCT AGGCATGGGG CCACCATTAG GCTGGTGATC CTGGAAGCTC TAAGAAAGCA
  AGCTGAGCAA ACCATGAAGG GCCAGCCAGT AAGAAACACT CTTCCGCCGC CTCTTCTTCA
  K
  TTTCTGTTTC AAGGTTCCTG TCCTATTTGA GTTCATGTCC TGACTTCCCT CACTGATGGA
  CCATGATGTG GAAGTGAAGC CAAAACAAAC TCTTCCTCTT CAAGTTGCTG TTGGTCACGG
  TGTTTCATCA CAGCAACAGA AACCCTGACT AAGACATGCT GCAAGGAACT TGCCCATGGA
  GCCATCTCTC CAACCTTGAA                                            
  
  K = G/T
  

  
  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
ss323926891	CHEV_12_17686491	CHEVERUD	SCREENING_POP	f	SNP	T	G
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs223912080					SNP	T	G