rs108631478 SNP Detail

Summary

• ID
  rs108631478
• Variation Type
  SNP
• Alleles
  A/G

• Created in dbSNP Build
  132
• Last Updated in dbSNP Build
  142
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr1:181655151 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                        TGTAT GTGTGTATAT GTATATGTAT
  R
  TGTATGTGTA TGTGTATGTG TATGT                                      
  
  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	129X1/SvJ	A/J	DBA/2J
ss146399229	ENSMUSSNP1346129	ENSEMBL	ENSEMBL_Sanger	f	SNP	G	A	G
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J
rs108631478					SNP	G	A	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr1:181655151 () rs orientation: forward

Symbol	Name	Function Class
Lbr	lamin B receptor	Intron
Rr424796	regulatory region 424796	166 bp proximal
Rr424797	regulatory region 424797	860 bp proximal
Rr424798	regulatory region 424798	950 bp proximal
Rr424799	regulatory region 424799	1272 bp proximal