rs262635661 SNP Detail

Summary

• ID
  rs262635661
• Variation Type
  SNP
• Alleles
  A/G

• 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
  Chr8:13334799 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              CGTAACACCA CAGAGTGCTG
  CAAGTCAAGA CACTGTAGAC ATACTCCTGA AGTCAGGATG ACGCCTGGGT CTGAGCCATA
  TAACTCCTAA AGTCACCCTC CACCCCCAGT GTATGACAAC TTAGCTTCAC TTACTGCAAA
  GAGCCTACGT CATAGACACA AGTACATCAG GCACTCACCG ACTTTTTGAA TGACCTCTAT
  R
  TTAGAGAGTG GGCAGAGGTG GAGACAGGGA AATAATCAGA CCCCTCCGAT ATATTAAAAC
  TGGCTTATCT ATATAGGATA CCCCCACCAA CTGCAGACCT CAGGAGAGTA CCAACATGTG
  CAGCAGTGTA TTACACACAG GAGGAGCCAG GAGCTGGCAC CACAGTCACA TGGTCTGATG
  TTAGCCTTTA CAGATTAAAC                                            
  
  R = A/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
ss322505797	CHEV_8_13284799	CHEVERUD	SCREENING_POP	f	SNP	G	A
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs262635661					SNP	G	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr8:13334799 () rs orientation: forward

Symbol	Name	Function Class
9530085L11Rik	RIKEN cDNA 9530085L11 gene	553 bp downstream
Dcun1d2	defective in cullin neddylation 1 domain containing 2	within coordinates
Gm25014	predicted gene, 25014	1585 bp upstream
Rr659902	regulatory region 659902	1382 bp distal