rs224651002 SNP Detail

Summary

• ID
  rs224651002
• Variation Type
  SNP
• Alleles
  G/T

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

Genome Location and Flanking Sequence

• Location
  Chr8:13334443 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              ATCTTAAAAA CACGGTGTTC
  ACTGAAATAA CCAGACACAA AGGCCATACA GTATAGAAAA TGCTATATGC TATGTGTGGA
  ATATGCAAAT TCGTAGGTTA GTAGCTACCA GGGGCTGAGG GGGAGGGAGG AACTTGGAAA
  TGCTTATGGG TACATGGTTT TCTTTGAGGT GATGAAATGT TTTGGAACTA GATGGGGTGG
  K
  GTGCACAGTA CTGGGACCAC ACTAATCACT ATAAACTTGT ACCCTAAAAG AAAACTTCAG
  GATAGCAAGC AAGAACCTCC AGGTCTACCC ACCGGATAGG TCTCTGGAGC AGCCACACTA
  TTATTATTAT TATTATTATT ATTATTATTG ACAAGCGTAA CACCACAGAG TGCTGCAAGT
  CAAGACACTG TAGACATACT                                            
  
  K = G/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
ss322505789	CHEV_8_13284443	CHEVERUD	SCREENING_POP	f	SNP	T	G
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs224651002					SNP	T	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr8:13334443 () rs orientation: forward

Symbol	Name	Function Class
9530085L11Rik	RIKEN cDNA 9530085L11 gene	909 bp downstream
Dcun1d2	defective in cullin neddylation 1 domain containing 2	within coordinates
Gm25014	predicted gene, 25014	1229 bp upstream
Rr659902	regulatory region 659902	1026 bp distal