rs108147932 SNP Detail

Summary

• ID
  rs108147932
• Variation Type
  SNP
• Alleles
  C/G

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

Genome Location and Flanking Sequence

• Location
  Chr4:106966448 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      T GTGTCTGTGT CTGTGTCTGT GTCTGTGTCT GTGTCTGTGT
  CTGTGTCTGT GTCTGTGTCT GTGTCTGTCT GTGTCTGTGT CTGTCTGTGT CTGTGTGTGT
  S
  TGTGTCTGTG TCTGTGTCTG TGTCTGTGTC TGTGTCTGTG TCTGTGTCTG TGTCTGTGTC
  TGTGTGTGCT GTGCAGAGTA GGCCATCAGT AGCTGTGTTT A                    
  
  S = C/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	A/J	DBA/2J
ss147175528	ENSMUSSNP4630097	ENSEMBL	ENSEMBL_Sanger	f	SNP	C	G
SNP Consensus Information
SNP					Consensus Type	A/J	DBA/2J
rs108147932					SNP	C	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:106966448 () rs orientation: forward

Symbol	Name	Function Class
Cdcp2	CUB domain containing protein 2	Intron
Rr596924	regulatory region 596924	305 bp distal
Rr596925	regulatory region 596925	within coordinates