rs221502756 SNP Detail

Summary

• ID
  rs221502756
• Variation Type
  SNP
• Alleles
  C/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
  Chr4:141445973 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              AATATCATTA ATACAACTCC
  ACCCTTAAGC ATGACATCAA ATGTCTTCTA GTATCGCAGA GTGTGGTGGC TCACACACTT
  TTTTTATTTT TGTTTGTGTT TTTTTGAGAC AGGGTTTCTC TGTGTAGCCC TGGCTGTCCT
  GGAACTCACT CTGTAGACCA GGCTGGCCTC GAACTCAGAA ATCCGCCTGC CCCTACCTCC
  S
  GAGTGCTGGG ACTAAAGGTG TGCGCCACCA CGCCCGGCTT GGCTCACACT CTTAACCCCA
  GCAATCGGGA GGCAGATCTC TGGGAGTTCG AGGCCAGCCT GGTCTGCAGA GTTCCAGGAC
  AGCCAGGGCT ACACAGAGAA ACCCTGTCTG GAAAAGCAAA GCAAACCAAA CCAAAGCAGA
  ATTTTTTGGT ATCTGAAAGA                                            
  
  S = C/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
ss321389258	CHEV_4_141274577	CHEVERUD	SCREENING_POP	f	SNP	G	C
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs221502756					SNP	G	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:141445973 () rs orientation: forward

Symbol	Name	Function Class
Ddi2	DNA-damage inducible protein 2	Intron
Rr398662	regulatory region 398662	625 bp upstream
Rr603862	regulatory region 603862	1432 bp proximal