rs252007500 SNP Detail

Summary

• ID
  rs252007500
• Variation Type
  SNP
• Alleles
  G

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

Genome Location and Flanking Sequence

• Location
  Chr4:109238714 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                    AGGAGCAAA GGGAAAGGAT GGTTTGTTGA
  AAAGATCATT GATTAGGGAT CTTAAATTCA TATTCTGGTC AGCCCCAGTC TCAGTTTGtg
  aactgcagtg tcacagatgc tcagcaagca ctctctccac tgagcgacat ttccagcccT
  G
  TTGGttttgg atagtgctcc atgtagctta acctggcctc agaccaaatt cctcatattc
  ctacttccta cccacatctc ccaaatgcta gcattaaccc caggcttgat tttgttttcc
  tttgtttggg ggtttgtttg tttggatttt                                 
  
  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	LG/J	SM/J
ss321253917	CHEV_4_109054122	CHEVERUD	SCREENING_POP	f	SNP	G	G
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs252007500					SNP	G	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:109238714 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Eps15	epidermal growth factor receptor pathway substrate 15			Intron
				Noncoding-Transcript-Variant
Rr597307	regulatory region 597307			887 bp proximal