rs46699892 SNP Detail

Summary

• ID
  rs46699892
• Variation Type
  SNP
• Alleles
  G/T

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  132
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr8:94268125 (GRCm39)
• SNP Orientation to the Genome
  reverse

• SNP Reference Flanking Sequence

                      G TAGTAAACTC AGTGCTCCAA GGTATGCTAA TCATAAAACA
  GATAGCCACA TTCCTTCCTC CACCCACCCG CTTCCTGGGT TCAAAGAGTG TTCATTCAAA
  K
  AAAGTCACCC TGACCCACCC TGACCATTGC TGGAACCCAC TATGCAAAGG TGCTATTGCT
  AGGGGCTCTT AGATTGTTAG GGGCTCTTAG AAACTGTCTT G                    
  
  K = G/T
  

  
  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	A/J	DBA/2J
ss139132978	ENSMUSSNP6575562	ENSEMBL	ENSEMBL_Sanger	f	SNP	G	T
SNP Consensus Information
SNP					Consensus Type	A/J	DBA/2J
rs46699892					SNP	G	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr8:94268125 () rs orientation: reverse

Symbol	Name	Function Class
Rr382481	regulatory region 382481	within coordinates