rs215384779 SNP Detail

Summary

• ID
  rs215384779
• 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
  Chr13:58639021 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              GGTGTAGCCA TTTTGGAAAC
  CAGCCCAGAG GCTTCTCAAG AAGCTTGGAA GTGCTGTGTG ATCCCTCGAC GACGCTTCCC
  CTGAGCTCAC ACCCCCAAGG CTCCTGCCCA TGCCGAGACA CTTAACACAC CCAGTGCTCA
  TTGCTGTTCT GTTCACAACA GCCAGGAAAT GCACACAGCC CCGGGAAAAT AATTTAATCC
  R
  ATCATTGTCA AAACATTTCC CGAATGTATC CCGGTGCACT CCCAGAGGAG TACAGATTCT
  TCGTCACCTC ACAGTGATGT CCTTTGGGTG TCACCAGGCT TACGAGCGTA CGTTTCCGTC
  ACGGATGGGG GTGGGATTCA TGGGACCCCT CCAACCCTGG AAGGTTAATT ACCATTGCTC
  AATTAAAGAG CAGGCAACCG                                            
  
  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
ss324353808	CHEV_13_58592568	CHEVERUD	SCREENING_POP	f	SNP	G	A
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs215384779					SNP	G	A