rs264371802 SNP Detail

Summary

• ID
  rs264371802
• Variation Type
  SNP
• Alleles
  A/G

• Created in dbSNP Build
  137
• Last Updated in dbSNP Build
  142
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr2:104515190 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                        ACATT GCCAGCTGAG GCATATCCCC
  R
  ACCTCTGCAG CTGTTTTGGT TGGTT                                      
  
  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	LG/J	SM/J
ss320445329	CHEV_2_104525002	CHEVERUD	SCREENING_POP	f	SNP	G	A
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs264371802					SNP	G	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:104515190 () rs orientation: forward

Symbol	Name	Function Class
Cpgi12000	CpG island 12000	475 bp proximal
Rr562107	regulatory region 562107	741 bp proximal
Rr562108	regulatory region 562108	1988 bp proximal
Tcp11l1	t-complex 11 like 1	Intron