rs245889596 SNP Detail

Summary

• ID
  rs245889596
• Variation Type
  SNP
• Alleles
  A/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
  Chr13:58637484 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                    CCTGGAGTT TTGTAGGACA AAGGTCAACT
  GCATTTGTGG CAACAAGGGA AGATTGGAAA GGCTGAAAAG TCAAAATAAT ATATACATTG
  TATAAAGTTC TTCCTAAgtg tgtgtgtgtg tgtgtgtgtg tgtgtgtgtg tgtgtgtgtg
  W
  gagtgtgtgt AGTTTTAGAT GGCAAACTAG GAAGAAAGTT ATTCCTGAGA TGTCCTTTTG
  GAAAGACACT TTCATGTTGA GAGTTCAGAA ATCCAAGTAC TCAAATCACA GTGTCCATCT
  TTGGCTGCAA ACCCACAATT CTTCAGATTA                                 
  
  W = A/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
ss324353801	CHEV_13_58591031	CHEVERUD	SCREENING_POP	f	SNP	T	A
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs245889596					SNP	T	A