rs108054953 SNP Detail

Summary

• ID
  rs108054953
• Variation Type
  SNP
• Alleles
  C/T

• Created in dbSNP Build
  132
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr13:56527655 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              GTCCTTGGGG GAGCTGTCAC
  TGCCTGTGAG GTGGGAAGCA GAGGGGGCAG TAAGATAGAT GCTTTCTCTG CCAGCCATTC
  CCACGCCCAC CTGGCTGAGT TCTCTCTGGA GTCAAGGCTA CCTGGAGCCG ATAGGTCTGC
  TCGACATGGC CGGTGAGTTT GCCAACCTAA CCTGGCAGGA CCAATGCTTC TGACCCCTGC
  Y
  CTTTGTGAAA TCAGCGAGAT AAGGTGGTGC TCTCCTGCTG TCCTTTGGCA GTAAGAAGCT
  GGGGGGCTTC ACAACCCCTT GGGTCATCCC CTGCCTCCTC TTTCTCAAAG ATGAGCCCCA
  TCCAGGTCTT CGGCTCCCTC TTAGCTATCC TGCCCACCCA TCTACCCTAC GCCCTGCCAC
  TGCTCATGGC TGTGAGAGAG                                            
  
  Y = C/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	129X1/SvJ	A/J	DBA/2J
ss149044552	ENSMUSSNP7058423	ENSEMBL	ENSEMBL_Sanger	f	SNP	C	T	C
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J
rs108054953					SNP	C	T	C