rs49915224 SNP Detail

Summary

• ID
  rs49915224
• Variation Type
  SNP
• Alleles
  C/T

• 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
  Chr2:147783739 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        TTGGTTCCTA GTAGTTCTTA GACCTGCCCA GACTTCCCTG
  CAGCCCAGAA AAGAGCCTCA CTATCCTTGC TCCTTATTCA CCCATAGACA TACTGGGAAA
  Y
  TCACAGAGGT TGTCACACTG AGCTGATTAG GACCACTTAC CAGGGACTGT AGGGCCCAAC
  TCCGGTGACA CCTGAATGAG TAAGTGCCAG ACAGCCACA                       
  
  Y = C/T
  

  
  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
ss147906880	ENSMUSSNP3246525	ENSEMBL	ENSEMBL_Sanger	f	SNP	C	T
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J
rs49915224					SNP	C	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:147783739 () rs orientation: forward

Symbol	Name	Function Class
Rr566828	regulatory region 566828	722 bp proximal