rs46897698 SNP Detail

Summary

• ID
  rs46897698
• Variation Type
  SNP
• Alleles
  A

• 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
  Chr6:139436967 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      T ATTAAAATAT ATAGCATATA TAAATATGTG CATGACAGTC
  ATGTGAAAAT ACTTGTGGCA CATATGAAAT ATGTGTGTAA TACATGGAAA AGCATACATA
  A
  CATATAGAAA GATATGGATG AAATAAAGAT ACAGGTGATG ATCATGTGAA ATATCCATGT
  ACATATGAAA ATATGCACAA TACACCTATT AAAACGTACA T                    
  
  A = A
  

  
  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
ss133916358	ENSMUSSNP1825090	ENSEMBL	ENSEMBL_Sanger	f	SNP	A
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ
rs46897698					SNP	A