rs239115778 SNP Detail

Summary

• ID
  rs239115778
• 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
  Chr13:5676277 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TTGCAGAGAG AATCTTTTCT
  GATGATGACT GAGCAAGTCA GTGCTCTATG AGTATAGCAG AATGTTGTTA GGAGTTCTTT
  TATGGCTATA TTCTCTTTTT AATTATTTAT TTTATTTATT TCCATTTCAA ATGTTGCTTC
  CCTCCTGGTC CCTGCTCCCA GAGTTATGCA GCACATCCCC CTTCATCTTT GCCACTGAGA
  K
  AGTGATCTTC CCCCCATCCC CATATCCACC TTCTTTGGTG CTTTTCTTTA TCAGAACAGA
  CTATGCCGGG GCCTAGTAAA CACAGAAGTA GATGCTCACA GTCAGCTATT GAATGGATCA
  CAGGGCTCCC AATGGAGGAG CTAGAGAAAG AACCCAAGGA GCTAAAGGGA TCTGCAACCC
  TCTAGGTGGA ACAACATTAT                                            
  
  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
ss324222368	CHEV_13_5625524	CHEVERUD	SCREENING_POP	f	SNP	T	G
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs239115778					SNP	T	G