rs51045467 SNP Detail

Summary

• ID
  rs51045467
• Variation Type
  SNP
• Alleles
  C

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr4:137857519 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        GTTCATGATG CATGTATTCA ACATGCCTTC CTGAAAATAT
  GCTATCTTAT ATCTCAGGAA CTGAGAACCT GGGTCCAGAC TTTTTTTTTT TCTTTTTTTT
  C
  TTTTTTTAAG ATTTATTTAA TGTGTATACA TTGCTGTCTT CAGACATACC AGAAGAGGGC
  ATCAGATCCT TTCACAGATG GTTGTGAGCC ACCATGTGG                       
  
  C = C
  

  
  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
ss147633689	ENSMUSSNP4094871	ENSEMBL	ENSEMBL_Sanger	f	SNP	C
SNP Consensus Information
SNP					Consensus Type	DBA/2J
rs51045467					SNP	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:137857519 () rs orientation: forward

Symbol	Name	Function Class
Eif4g3	eukaryotic translation initiation factor 4 gamma, 3	Intron
Rr602841	regulatory region 602841	121 bp distal
Rr602842	regulatory region 602842	45 bp proximal
Rr602843	regulatory region 602843	1046 bp proximal