rs45677916 SNP Detail

Summary

• ID
  rs45677916
• 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
  Chr2:32863199 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

             GCTCTGAGGA GGGCTTGGTT GGCAAGAACA TTCTCTCTTC TACCTGGGCT
  Y
  ACCTGACCTT GTTTCTGAGC CCATATGGCT AAGTCCCTTT CTGATCTCCC           
  
  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	A/J	DBA/2J	MSM/Ms
ss146405037	ENSMUSSNP3555473	ENSEMBL	ENSEMBL_Sanger	f	SNP	C	C	T
SNP Consensus Information
SNP					Consensus Type	A/J	DBA/2J	MSM/Ms
rs45677916					SNP	C	C	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:32863199 () rs orientation: forward

Symbol	Name	Function Class
Rr555133	regulatory region 555133	1622 bp distal
Slc2a8	solute carrier family 2, (facilitated glucose transporter), member 8	within coordinates