rs107952095 SNP Detail

Summary

• ID
  rs107952095
• Variation Type
  SNP
• Alleles
  G

• Created in dbSNP Build
  132
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr1:185867171 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        CCCTTCAGCT CCTTGGGTGC TTTCTCTAGC TTCTCCATTG
  GGAGCCCTAT GTTCCATCCT ATAGATGACT GTGAGCATCC ACTTCTGTAT TTGCCAGGCA
  G
  TGGCATAGCC TCATATGAGA CAGCTATATC AGGGTCCCTT CAGCAAAATC TTGCTGGCAT
  ATGCAATAGT GTCTGGGTTT GGTGGCTGAG CAGGGTGGG                       
  
  G = G
  

  
  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
ss146452363	ENSMUSSNP5665489	ENSEMBL	ENSEMBL_Sanger	f	SNP	G
SNP Consensus Information
SNP					Consensus Type	DBA/2J
rs107952095					SNP	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr1:185867171 () rs orientation: forward

Symbol	Name	Function Class
Rr425453	regulatory region 425453	1779 bp proximal