rs263921170 SNP Detail

Summary

• ID
  rs263921170
• 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
  Chr4:152448776 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              CCCAAGAGAC ACACACACAA
  GAATATACTC AGCATGGGGT GGGCATGGCG GTGCATACCT CTGATCCCAG TACTTGGGCT
  GCAGAGACAG ACTGATCTCT GTGAGTTCAA GAGCAGCCTG ATCTACACAG CAAGCTCCAG
  GACAACCCTG GGCCACACAG AGAGCTCTTG TCTCAAAGCT CTCTCTCTTT CCTCTCTCTC
  T
  TTTGAGAGCA CTGGCTGCTC TTGCAGAGGG CCTGGGTTAG GTTCTCAGTA CCCACAACAC
  TGCTTACTGC CTCCTGTAAT TCTGGTTCTC GGTGATCAGA TACCCTCTCC TGGCTTCTGT
  GGGTACCAGG AACATATATG GTACACATAC ATGCATGCAA ACATGCATAC ATGCATACAT
  GCATGCAAAC ACACATACAT                                            
  
  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
ss321434338	CHEV_4_151738428	CHEVERUD	SCREENING_POP	f	SNP	T	T
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs263921170					SNP	T	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:152448776 () rs orientation: forward

Symbol	Name	Function Class
Chd5	chromodomain helicase DNA binding protein 5	Intron
Rr605861	regulatory region 605861	961 bp proximal