rs47670919 SNP Detail

Summary

• ID
  rs47670919
• Variation Type
  SNP
• Alleles
  C/T

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  138
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr2:147217146 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                        TGTCA GTGGCTCCAC CAGGTTGGTG
  Y
  GCCCCTACCC CACTCCCCCC CTGGC                                      
  
  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	A/J
ss147887050	ENSMUSSNP1689737	ENSEMBL	ENSEMBL_Sanger	f	SNP	T	C
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J
rs47670919					SNP	T	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:147217146 () rs orientation: forward

Symbol	Name	Function Class
Cpgi12389	CpG island 12389	1329 bp distal
Pax1	paired box 1	174 bp downstream
Rr39113	regulatory region 39113	1855 bp proximal
Tssr20631	transcription start site region 20631	1363 bp downstream
Tssr20632	transcription start site region 20632	1307 bp downstream
Tssr20633	transcription start site region 20633	1271 bp downstream
Tssr20634	transcription start site region 20634	1178 bp downstream
Tssr20635	transcription start site region 20635	302 bp upstream