rs262677628 SNP Detail

Summary

• ID
  rs262677628
• 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
  Chr11:101242300 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        TACCTAGTGC ATCTTCCCTG ATCCTCATCA AGGAAGTAGC
  CAGCGTCAAA GTTGCTTAGC ACCTCACATG CGCCTATCCA ACGCTCCCCC GAGCCTCCAT
  R
  AATGGACATG GCTCAGCCTT ACACACAGCT CAGCTCCTCC CAGGCTTCTG CTCAACCTGT
  GTGTGAGTCA CTGAAAGTCA CTGGAGGATT GTGGTGCCT                       
  
  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
ss323832861	CHEV_11_101212788	CHEVERUD	SCREENING_POP	f	SNP	G	A
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs262677628					SNP	G	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr11:101242300 () rs orientation: forward

Symbol	Name	Function Class
Gm11618	predicted gene 11618	762 bp upstream
Gm11619	predicted gene 11619	1835 bp downstream
Gm55747	predicted gene, 55747	1868 bp downstream
Gm74449	predicted gene, 74449	1750 bp downstream
Rr247835	regulatory region 247835	within coordinates