rs46567436 SNP Detail

Summary

• ID
  rs46567436
• Variation Type
  SNP
• Alleles
  C

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  142
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr10:3186858 (GRCm39)
• SNP Orientation to the Genome
  reverse

• SNP Reference Flanking Sequence

                                        GCAGC TGAGTTCCTT CCTGCCCCAC
  C
  CTGCAAAGCA CTGAGACTTG AGATA                                      
  
  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	129X1/SvJ	A/J	LG/J	SM/J
ss146753864	ENSMUSSNP1660710	ENSEMBL	ENSEMBL_Sanger	f	SNP	C	C
ss323243695	CHEV_10_7109683	CHEVERUD	SCREENING_POP	f	SNP			C	C
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	LG/J	SM/J
rs46567436					SNP	C	C	C	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr10:3186858 () rs orientation: reverse

Symbol	Name	Function Class
Gm6667	predicted gene 6667	1825 bp upstream
Rr230143	regulatory region 230143	1582 bp proximal