rs51484259 SNP Detail

Summary

• ID
  rs51484259
• Variation Type
  SNP
• Alleles
  T

• Created in dbSNP Build
  128
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  ChrX:111860466 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TATTTTTATT TAAGAATGTG
  TAATAGAGAT GGTAAAGGAT TGCGTTTCCG TGTTAAAGGA AACCTATCCT GTCCAAACCT
  CACCCACAAA GGCATTGCAA GTTTCTATCT TTCTGGGGTT TACCTTTGTC TGACCTTGGC
  TCCTTGCTTT CTGCTCTATT GGGGACAATG GCAGGTGAGA AGTCGGGTGA TTGATATATG
  T
  GAAAAAGCAA ATGCAAACTG CCCACACTGG GATTGTTCTT TGTCAACACA CATAGTTGGC
  TGTAAATGCA GTATTTCCAT TAACACCATA TGTTAGACAA TTAATTGTAT CTATTGGATC
  AAAGTCTTAG TTTCTTCTTA CCTACTGTGG AAGCTAGTGA GCAGAATCAC TGTATTTAGT
  GGGTCCCATA TAAAGATGAA                                            
  
  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	129X1/SvJ	A/J
ss134277746	ENSMUSSNP5621194	ENSEMBL	ENSEMBL_Sanger	f	SNP	T	T
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J
rs51484259					SNP	T	T