rs47618877 SNP Detail

Summary

• ID
  rs47618877
• Variation Type
  SNP
• Alleles
  G

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr10:8858287 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TGTGAATTTT ATACTATTTA
  AATCACATCT CAGCGATTCT CTCTAAAATG TGATGTTCAA TTCAAGACTT TTTTTTTTTT
  TGCCTACAAT TGGATTAGAA TTTTCTCACT GGAACTATTT GTTATTCTGA GTTATTTATA
  TTTTAAGGAA AAGATTCATT TTTATTCTTT ACTGGTGTGT GTGTGTGTGT GTGTTTGTAT
  G
  CATGTGTATG TGGGTGCCCA TTGAATTCAG AAGAGGGCAC TAGACCCTTG GAGAAGGTAC
  CACAGGCAGC TGTGGGCCAT CCAATGTGGG GACCTCTACA TGAGCAGTTT GTGCTCTTAA
  CCAATGAGGA ACCTCGCCAG CTTCTGCAGA CGTGCACTTA TCTGTCTATT TATATCCCTG
  TTATGTTCAT TTATTCTCAT                                            
  
  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	129X1/SvJ
ss146769166	ENSMUSSNP485342	ENSEMBL	ENSEMBL_Sanger	f	SNP	G
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ
rs47618877					SNP	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr10:8858287 () rs orientation: forward

Symbol	Name	Function Class
Rr223851	regulatory region 223851	314 bp proximal
Rr223852	regulatory region 223852	791 bp proximal