rs107754682 SNP Detail

Summary

• ID
  rs107754682
• Variation Type
  SNP
• Alleles
  C

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

Genome Location and Flanking Sequence

• Location
  ChrX:44397471 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      C AAGTAGGCTT CATTCCAGCG ATGCAGGGAT GGTTTAATAT
  ATGGAAATCC ATCAATGTAA TCCACTATAT AAACAAACTC AAAGACAAAA ATCACATGAT
  C
  ATCTTGTTAG ATGCTGAGAA AGCATTGGAC AACATTCAAC ACTCATGATA AAAGTTTTGG
  AGAGATCAGG AATTCAAGGC TCATACCTAA ACCTAATCAA A                    
  
  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
ss134407072	ENSMUSSNP1133785	ENSEMBL	ENSEMBL_Sanger	f	SNP	C
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ
rs107754682					SNP	C