rs49192863 SNP Detail

Summary

• ID
  rs49192863
• 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
  Chr2:153419939 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        GTTTTTTGGA GAGTCGGTTG GATGGTGTTT GGGGGGTGGG
  GGTGGGGGGC AAACATGTGA AGGAACGTTT CGCTGAAGCA GATACAGGAG AGAGGATGTT
  Y
  TGCTAAAGCA AGCACATGAA AGGATATGTG ACGAAGGATT CTTTGCTAAC AACACACATG
  CATTGGTCTG CCTTACGTTG TGTAGTTGAG CTGCATTGG                       
  
  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	DBA/2J
ss147997144	ENSMUSSNP577094	ENSEMBL	ENSEMBL_Sanger	f	SNP	C	T
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	DBA/2J
rs49192863					SNP	C	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:153419939 () rs orientation: forward

Symbol	Name	Function Class
Rr567686	regulatory region 567686	1526 bp distal
Rr567687	regulatory region 567687	455 bp distal
Rr567688	regulatory region 567688	293 bp distal