rs237625178 SNP Detail

Summary

• ID
  rs237625178
• Variation Type
  SNP
• Alleles
  T

• 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
  Chr4:141446322 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TGGAAAAGCA AAGCAAACCA
  AACCAAAGCA GAATTTTTTG GTATCTGAAA GAGCTTCCAT TTACTGGGGA TTGGGGAGCT
  AAACTGTTTT CTCTTTTGAC AAGTGCTGGG GATCTAATGC ATAGCAGGCA AGCACTCTCT
  CTACCAGAGC TACCCCTAAC CCAGTACATC TTATTTTTCT GAAACAAGGT TTCCTATACA
  T
  ACCAGGCTAG CCTAGATCTT CCAGCTCCAC CTCAGCCTGC CTCTCAAGTG CTGGGATTAA
  CAATGCGAGT CACCATGCTC AGCACCCCAA CAAAAACCTG AGACAGGTTC TTACCGCGCA
  GGCTCAGCTG TCCTGAGACC TGAAATGGAG TCCAGGCTGG CCTTGAACTC TCAGTCTCAA
  ATATCAAACA AAAACAATCA                                            
  
  T = 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	LG/J	SM/J
ss321389259	CHEV_4_141274926	CHEVERUD	SCREENING_POP	f	SNP	T	T
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs237625178					SNP	T	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:141446322 () rs orientation: forward

Symbol	Name	Function Class
Ddi2	DNA-damage inducible protein 2	Intron
Rr398662	regulatory region 398662	276 bp upstream
Rr603862	regulatory region 603862	1083 bp proximal
Rr603863	regulatory region 603863	1711 bp proximal