rs46665532 SNP Detail

Summary

• ID
  rs46665532
• Variation Type
  SNP
• Alleles
  T

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr9:98769545 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              ATTTCTGAGT TTGAGTCCAG
  CCTGGTCTAC AGAGTGAGTT CCAGGAGAGT CAGGGATACC CAGAGAAACC CTGTCCCAAC
  CCACCCCCAA CCAAATAAGT AAATAAATAA ATAAATAAAT AAATAAAATT TGTTACCGGC
  TTTAAATACC AAGCTTTACC TCCAAGAAAC AAAAGAAGAT TCATTTTCAT AATTTCCATT
  T
  CCATTTTATT TTATAAATAA AGAGAATTTC TTGGTGGGGA TGGGACAAAG AGGTGACAAA
  AACCTGACTC GGGTGGGAAA ATAATGATAC CACAAATAAA GGCAATAAAA ACCAAAGGGA
  CTTCCAAGGA CTGATTCTTT GTCTAAACCA TCAAAACGGC CAAAATTCCC CTGCCACACC
  ACCCTCCGTG CCTCAAGATC                                            
  
  T = 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	DBA/2J
ss136842190	ENSMUSSNP499148	ENSEMBL	ENSEMBL_Sanger	f	SNP	T
SNP Consensus Information
SNP					Consensus Type	DBA/2J
rs46665532					SNP	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr9:98769545 () rs orientation: forward

Symbol	Name	Function Class
Gm33700	predicted gene, 33700	719 bp upstream