rs47614356 SNP Detail

Summary

• ID
  rs47614356
• Variation Type
  SNP
• Alleles
  C/G

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  132
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr4:27132999 (GRCm39)
• SNP Orientation to the Genome
  reverse

• SNP Reference Flanking Sequence

                      T GATGGTAAAT TTCTGTGTAA GGGAGTGACT TAGCTTTTAC
  AATCTTGCTG AATTCTAAAC CCTTGATCTT GGTCAAGGAT GCCCTTGGAG TGTTGGAACA
  S
  TGGCGGAAGG CTTTAGCCAT GTCAGAGCAC TTATAGGAAA ATACTGAAAG AGAGCACGTG
  GATCCATACT CTAGACTAGC GTGGTACTGG AACTCGGGAA T                    
  
  S = C/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	MSM/Ms
ss137931952	ENSMUSSNP5422821	ENSEMBL	ENSEMBL_Sanger	r	SNP	G		G	G
ss137932975	ENSMUSSNP4590098	ENSEMBL	ENSEMBL_Sanger	r	SNP	G		C
ss137937200	ENSMUSSNP2721522	ENSEMBL	ENSEMBL_Sanger	r	SNP	G	C	C
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J	MSM/Ms
rs47614356					SNP	C	G	G	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:27132999 () rs orientation: reverse

Symbol	Name	Function Class
Rr376259	regulatory region 376259	within coordinates