rs46710764 SNP Detail

Summary

• ID
  rs46710764
• Variation Type
  SNP
• Alleles
  C/G

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  138
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr2:120872105 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                        AATAG TCTAGAGGGC TGAGAGAGGG
  S
  AAGTTGACCA ATAAGAGACA TCTAG                                      
  
  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	129X1/SvJ	A/J	LG/J	SM/J
ss147377009	ENSMUSSNP2718274	ENSEMBL	ENSEMBL_Sanger	f	SNP	C	C
ss320481403	CHEV_2_120867360	CHEVERUD	SCREENING_POP	f	SNP			G	C
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	LG/J	SM/J
rs46710764					SNP	C	C	G	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:120872105 () rs orientation: forward

Symbol	Name	Function Class
Rr563767	regulatory region 563767	242 bp distal
Rr563768	regulatory region 563768	331 bp distal