rs51951970 SNP Detail

Summary

• ID
  rs51951970
• Variation Type
  SNP
• Alleles
  T

• Created in dbSNP Build
  128
• Last Updated in dbSNP Build
  132
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  ChrX:44397413 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      T TAATTAAATT ATTACAAACT GAATCCAAGA ACACATCAAA
  ATGATCATCC ATCATGATCA AGTAGGCTTC ATCCCAGCGA TGCAGGGATG GTTCAATATA
  T
  GGAAATCCAT CAATGTAATT CATTATATAA ACAAACTCAA AGACAAAAAT CACATGGTCA
  TCTCCTTAGA TGCCAAGAAA GCATTTGACA AAATCCAACA C                    
  
  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
ss145877446	ENSMUSSNP122571	ENSEMBL	ENSEMBL_Sanger	f	SNP	T
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ
rs51951970					SNP	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: ChrX:44397413 () rs orientation: forward

Symbol	Name	Function Class
Rr7424	regulatory region 7424	473 bp proximal