rs51690497 SNP Detail

Summary

• ID
  rs51690497
• Variation Type
  SNP
• Alleles
  G

• Created in dbSNP Build
  128
• Last Updated in dbSNP Build
  142
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr1:181654610 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                        ATCTC TCGACTGACA CTCGACATCT
  G
  CCTGTACGTA TGCATGGTTA TTTTC                                      
  
  G = 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	DBA/2J
ss146399225	ENSMUSSNP2789640	ENSEMBL	ENSEMBL_Sanger	f	SNP	G	G
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	DBA/2J
rs51690497					SNP	G	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr1:181654610 () rs orientation: forward

Symbol	Name	Function Class
Lbr	lamin B receptor	Intron
Rr424796	regulatory region 424796	707 bp proximal
Rr424797	regulatory region 424797	1401 bp proximal
Rr424798	regulatory region 424798	1491 bp proximal
Rr424799	regulatory region 424799	1813 bp proximal