rs47846913 SNP Detail

Summary

• ID
  rs47846913
• 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 | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr2:153065838 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                        TTGCC CATCAGGACC AAATGCACCC
  R
  CTTCATCTTA GGTGTCACAC CTCAG                                      
  
  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
ss147988176	ENSMUSSNP305569	ENSEMBL	ENSEMBL_Sanger	f	SNP	G	A	A
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J
rs47846913					SNP	G	A	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:153065838 () rs orientation: forward

Symbol	Name	Function Class
Rr567581	regulatory region 567581	1905 bp distal
Rr567582	regulatory region 567582	1538 bp distal
Rr567583	regulatory region 567583	1513 bp proximal
Tspyl3	TSPY-like 3	mRNA-UTR
Tssr26887	transcription start site region 26887	1115 bp downstream
Tssr26888	transcription start site region 26888	1459 bp downstream
Tssr26889	transcription start site region 26889	1478 bp downstream