rs232635039 SNP Detail

Summary

• ID
  rs232635039
• 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
  Chr9:119183166 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              GATGTCCTAG CTTCGAATGT
  GCACAGAAGG AGGCAAGCAG ACCCCAAGGG ATGAACACAG TAAAATCAGA AAGAAGATGA
  ACATTTTAAC TGTCCTAAAC CAAATTTGCT TCTAAAGAGA GTACAAACAC GCGGCAGGCT
  CGTCCCCTTT GGGGAAGACT AACTCCTCCC CCCGTAGAGC TGTTTGCTCC CACCCCACAT
  Y
  CCGTCAAGCA TTTCTCTATC TGCAAACATT AACTCTGCTT TTTAAAAAAC GCAATGTCAG
  CTGCCCTTTT AACAGAGGCT ACTGATTTAA CAGAAGGCAG GTCCAACCCC ACCCTCCAAG
  GAGGACCAGG AGTTGACTGA TGCTTGTCCT GATAGAAACA GTTGGCCAAA ATGCCATCTT
  CCCTCATAAC CACTTCCCAC                                            
  
  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
ss323218990	CHEV_9_119263218	CHEVERUD	SCREENING_POP	f	SNP	C	T
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs232635039					SNP	C	T