rs46544743 SNP Detail

Summary

• ID
  rs46544743
• Variation Type
  SNP
• Alleles
  C/T

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr3:65843637 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TTTTCCTGGA AACACACCTT
  CAATTTGTTT TTTGCAAATT AAAGAGTATC ACTTTTGGGG GCTGGAGAGA TGGCTCAGTG
  GTTAAGAGCA CTGACTGCTC TTCCGAAGGT CCTGAGTTCA AATCCCAGCA ACCACATGGT
  GGCTCACAAC CATCTGTAAT GGGATCTGAT GCCCTCTCCT GCTGTGTCTG AAGACAGCAA
  Y
  GGTGTACTCA TATACAGAAA ATAAATAAAT CTTAAAAAAA AAGAAAGTAT CACTTTTGCT
  GATGCATAAT ATACCTTCTG TTATCATGAT CTTCAGGGAT GTTTTCCTAA AACTCTCAAA
  TCTCTTTCTT CATTGCACTA AAAATACTTG CATAGGTGGA ACTCACGACT TTTGGCAAAC
  GGTGAATTCA ACATCTTCTC                                            
  
  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	MSM/Ms
ss135254261	ENSMUSSNP646795	ENSEMBL	ENSEMBL_Sanger	f	SNP	T	T	T	C
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J	MSM/Ms
rs46544743					SNP	T	T	T	C