rs265871555 SNP Detail

Summary

• ID
  rs265871555
• 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
  ChrX:120754012 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              AACCTGATAA ACAGCTTCGG
  TGAAATAGCT GAATATAAAA TTAACTCAAA CAAGTCAATG GCTTTTCTCT ACACAAAGAA
  TAAACAGGCT GAGAAAGAAA TTAGGGAAGC AAAAACCTTT CTCAATAGTC ACAAATATTA
  TAAAATATCT TGGTGTGACT CTAACTAATG AAGTAAAAGG TCTGTATGAT AAGAACTTCA
  Y
  GTCTCTGAAG ATATACATTA AAGAAGATCT TAGAAGATGG AAAGATCTGC CATGCTCATG
  GATTGGCAGG ATCAATATTA TAAAAATGGC TATCTTGCTA AAAGCAATCT ACATATTCAA
  TGCAATACCC ATCAAATTTC CAACTCAGTT CTTCAATGAA TTAGAAAGAG CAATCTGCAA
  ATTTATCTGG AATAACAAAA                                            
  
  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
ss325960943	CHEV_X_118957924	CHEVERUD	SCREENING_POP	f	SNP	C	T
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs265871555					SNP	C	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: ChrX:120754012 () rs orientation: forward

Symbol	Name	Function Class
Rr395603	regulatory region 395603	1698 bp upstream