rs108929472 SNP Detail

Summary

• ID
  rs108929472
• Variation Type
  SNP
• Alleles
  C

• Created in dbSNP Build
  132
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr3:21726525 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        CTTGCATAGC TTGCTACAAG AAAGCCCAAG ACAGGTCAGT
  TTCTCTGCCG AAGAACTGCA TGGCTTGTAA AAGGTACATC TAACCCAAAC AATCACTACC
  C
  CCCCCCCACC CCCCCACCCC CCCACCCCCC CGTCTTTCCC TTAGACTCCA GGGTCTTCTT
  CAGGTTGGTA GACCTCTGAT CATTCAGTGT CTTCATTGC                       
  
  C = C
  

  
  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	DBA/2J
ss134683824	ENSMUSSNP6348482	ENSEMBL	ENSEMBL_Sanger	f	SNP	C
SNP Consensus Information
SNP					Consensus Type	DBA/2J
rs108929472					SNP	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:21726525 () rs orientation: forward

Symbol	Name	Function Class
Rr374653	regulatory region 374653	within coordinates
Rr574145	regulatory region 574145	within coordinates