rs264329754 SNP Detail

Summary

• ID
  rs264329754
• Variation Type
  SNP
• Alleles
  C

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

Genome Location and Flanking Sequence

• Location
  Chr2:103913201 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        CACATACACA CCCAATCACA CACCCACATA CACTCACACA
  CCCACACATA CACACACTGA CACACCCACA CACACCCATA CCCACCCACC CACACTCATA
  C
  ACTCACACAC ATTTACCTAC ACACCCACAC ATACACACCC AATCACACAC CCACACACAC
  TCACCCAAAC ACACTCACCC ACACTCACAT ACCCACACA                       
  
  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	LG/J	SM/J
ss320443672	CHEV_2_103923013	CHEVERUD	SCREENING_POP	f	SNP	C	C
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs264329754					SNP	C	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:103913201 () rs orientation: forward

Symbol	Name	Function Class
Cd59b	CD59b antigen	Intron
Rr562021	regulatory region 562021	889 bp distal
Rr562022	regulatory region 562022	within coordinates
Rr562023	regulatory region 562023	1166 bp proximal