rs51092561 SNP Detail

Summary

• ID
  rs51092561
• Variation Type
  SNP
• Alleles
  A/G

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  138
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr13:100006821 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                        ACTAG GAAGACCAAT CAGAAAACAA
  R
  CAACCACAAT GTGACTAACC CTATG                                      
  
  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	129S1/SvImJ	129X1/SvJ	CAST/EiJ	LG/J	NZW/LacJ	PWD/PhJ	SM/J
ss52683306	NES15524600	PERLEGEN	MM_PANEL2	f	SNP	A		A		G	A
ss145079766	ENSMUSSNP2880961	ENSEMBL	ENSEMBL_Sanger	f	SNP		A
ss324505384	CHEV_13_100640268	CHEVERUD	SCREENING_POP	f	SNP				G			A
SNP Consensus Information
SNP					Consensus Type	129S1/SvImJ	129X1/SvJ	CAST/EiJ	LG/J	NZW/LacJ	PWD/PhJ	SM/J
rs51092561					SNP	A	A	A	G	G	A	A

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
ss52683306	NES15524600	PERLEGEN	MM_PANEL	f	SNP	A/G