rs47838032 SNP Detail

Summary

• ID
  rs47838032
• Variation Type
  SNP
• Alleles
  A/G

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  142
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr1:170785147 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                        CCAAG TGCTGGGATT AAAGGCGTGC
  R
  CCACCATAGC CCATCTAATA TGTCC                                      
  
  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	129X1/SvJ	A/J	DBA/2J	LG/J	SM/J
ss146148838	ENSMUSSNP6207436	ENSEMBL	ENSEMBL_Sanger	f	SNP	A	A	G
ss320114959	CHEV_1_172887709	CHEVERUD	SCREENING_POP	f	SNP				A	A
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J	LG/J	SM/J
rs47838032					SNP	A	A	G	A	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr1:170785147 () rs orientation: forward

Symbol	Name	Function Class
Fcgr2b	Fc receptor, IgG, low affinity IIb	1039 bp downstream
Gm70986	predicted gene, 70986	within coordinates
Rr20517	regulatory region 20517	1254 bp proximal
Rr20518	regulatory region 20518	1854 bp proximal
Tssr14949	transcription start site region 14949	1317 bp downstream