rs49461452 SNP Detail

Summary

• ID
  rs49461452
• Variation Type
  SNP
• Alleles
  A/T

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

Genome Location and Flanking Sequence

• Location
  Chr9:52853445 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        TGTTGTACTT TGAAAGCAGC AAGCTTAGTG TGTCCTAGGG
  CAGAGCATAT CTGGCCAAGG AAAGGATTCT GGGAAGATCT GTGTCTCTGG CTGTAGGTCT
  W
  TGTGCAGATA ACCCAAAAGA TCTCTCCTTA GAACTATATA GTGTAAATGG TGTGTGTGTG
  TGTGTGTGTG TGTGTATGGT GTAAATGGTG TGTGCGTGTG                      
  
  W = A/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	129S1/SvImJ	CAST/EiJ	DBA/2J	FVB/NJ	KK/HlJ	NZW/LacJ	WSB/EiJ
ss61397871	NES16783024	PERLEGEN	MM_PANEL2	f	SNP	A	A	T	T	T	T	T
SNP Consensus Information
SNP					Consensus Type	129S1/SvImJ	CAST/EiJ	DBA/2J	FVB/NJ	KK/HlJ	NZW/LacJ	WSB/EiJ
rs49461452					SNP	A	A	T	T	T	T	T

Additional submitted assays for this SNP, where the strain of origin for observed alleles is not specified by the submitter

Assay ID	Submitter SNP ID	Submitter Handle	Population	ss orientation	Variation Type	Alleles
ss61397871	NES16783024	PERLEGEN	MM_PANEL	f	SNP	A/T