rs226876349 SNP Detail

Summary

• ID
  rs226876349
• 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
  Chr4:152448834 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              CTCTGATCCC AGTACTTGGG
  CTGCAGAGAC AGACTGATCT CTGTGAGTTC AAGAGCAGCC TGATCTACAC AGCAAGCTCC
  AGGACAACCC TGGGCCACAC AGAGAGCTCT TGTCTCAAAG CTCTCTCTCT TTCCTCTCTC
  TCATTTGAGA GCACTGGCTG CTCTTGCAGA GGGCCTGGGT TAGGTTCTCA GTACCCACAA
  G
  ACTGCTTACT GCCTCCTGTA ATTCTGGTTC TCGGTGATCA GATACCCTCT CCTGGCTTCT
  GTGGGTACCA GGAACATATA TGGTACACAT ACATGCATGC AAACATGCAT ACATGCATAC
  ATGCATGCAA ACACACATAC ATACATACAT ACATACAAGC ATACACATTT TGTTTTTGAG
  ACAAGGTCTT GCTATGCAGT                                            
  
  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
ss321434339	CHEV_4_151738486	CHEVERUD	SCREENING_POP	f	SNP	G	G
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs226876349					SNP	G	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:152448834 () rs orientation: forward

Symbol	Name	Function Class
Chd5	chromodomain helicase DNA binding protein 5	Intron
Rr605861	regulatory region 605861	903 bp proximal