rs259710035 SNP Detail

Summary

• ID
  rs259710035
• 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
  Chr13:58636384 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              ACTCTCAGCT CCTCCTGCAC
  CATGACTACC TGGATGCTTC CATGTTCCCA CCTTGATGAT AATGGACTGA ACCTCTGAAC
  CTGTAAGCCA GCCCTAATTA AATGTTGCCC TTTATAATTC TTGCCTTGGC CATGGTATCT
  GTTCACAGCA GTAAAACTAA GACAGGAGGT CAATGCCTGG AAAACTACAT CAGTCAGGGC
  Y
  CGGACCGGAG AGACCCATGG GGCTCACAAC AATCCATTCT GCACCTCCAA GGTGAAGTGT
  GATGTTGAGG GCCAGGCAGA AGTGTGCCAG TTCTGAGAGT TCCTGAAGAA TAAATTATTT
  TATATTTAGG TCACAGAGAA ACAGGAAAGA TTTTGGTTCC TTGTTTTTGT TTTGTTTCAA
  GACAGGGTTT CTTTGTGTAG                                            
  
  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
ss324353799	CHEV_13_58589931	CHEVERUD	SCREENING_POP	f	SNP	C	T
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs259710035					SNP	C	T