rs213798218 SNP Detail

Summary

• ID
  rs213798218
• 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
  Chr13:25779744 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              CCTTTTTATA GACATAAGTA
  ACATTGCCAA ATTGTTTTTA TTTTGTTCCT ATGCTAGTGG GCCAATACTT TTCTCTATTT
  CGGGGGGGGG GGGTAATGGT ATAGTTATAT GATGTTTGGA GAAAAATCCA CAATATAACA
  CATGTTATAC ATGTCATGAG ACTAAATGTA TAGTAATATG TGGATAAGGT AGCTTACAAT
  R
  AAATTTACAG CAATAGTCTA TAATTTCATA GTGATTTCAT ATTGGCTCAC CCTTTGTCTA
  CAATCTGTGA ACATATTCCT TACCCTTTTC TGAGCATAGT TGACAGAATT AACAATATTG
  TAAAGGTCAC TTAGATTAGC ATAGGTATGT ATTTTGTACA TATAGATTGT GGAATCCAAG
  ATGGATATTC AATACTTCAT                                            
  
  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
ss324304525	CHEV_13_25687630	CHEVERUD	SCREENING_POP	f	SNP	G	A
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs213798218					SNP	G	A