rs45726146 SNP Detail

Summary

• ID
  rs45726146
• Variation Type
  SNP
• Alleles
  C/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
  Chr1:165429646 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        AAAAAAAACG GCAGAAAACA GAACCATAGG TCTGCAGACA
  ACCAACAGCT GACAATCTCC TCCCACTTTG GAAATCCCTG CATCCTTCTC AACCAATCAG
  Y
  ATGCAGCTGA GGGGAGGGGC GACCCTGCGA TTGTGTCTGT GTGGGGAGAC ACTATCTTTT
  CTCGGGCCAT CCACCCTGCT TCTGGATAAA TGTTCAGAG                       
  
  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	129X1/SvJ	DBA/2J
ss146003096	ENSMUSSNP1372452	ENSEMBL	ENSEMBL_Sanger	f	SNP	C	T
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	DBA/2J
rs45726146					SNP	C	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr1:165429646 () rs orientation: forward

Symbol	Name	Function Class
Mpzl1	myelin protein zero-like 1	within coordinates
Rr422396	regulatory region 422396	1094 bp proximal
Tssr14771	transcription start site region 14771	117 bp upstream