rs263325680 SNP Detail

Summary

• ID
  rs263325680
• Variation Type
  SNP
• Alleles
  C/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
  Chr13:25780095 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              ATTTTGTACA TATAGATTGT
  GGAATCCAAG ATGGATATTC AATACTTCAT CATGAAGACA ACAGACCTAA CTTATGGACA
  TCCAAATGGA CAGACTGCTA TGAATAGTCT TTTTTTTTCT ATGCTTTGGT CCAAGCACAA
  ATTCCTTGGG TTTTTAAGAT TTAGTTTTGT TGACATTTTG ATCTTCTGTA TCTGGTGCTA
  Y
  GCTGAATTTG TAAGAAGTCA TCTCTAAACT CAACAAAGAA AAGTTTAACA AGACAGTTCT
  TCTTAGAAGG GTTTCCGTGG CTAATCTCCT AGATATACAT TGATTTCTAT GGTAGAGAGA
  TGTAGGCATT AGGTAACACC AGAAAACTGT GCAGTTTCTA AGACTGTGAT TCCAGAAGTA
  TATTTCCAGT GTATGATTTT                                            
  
  Y = C/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
ss324304530	CHEV_13_25687981	CHEVERUD	SCREENING_POP	f	SNP	T	C
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs263325680					SNP	T	C