rs48535178 SNP Detail

Summary

• ID
  rs48535178
• Variation Type
  SNP
• Alleles
  A/G

• 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
  Chr13:58636106 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              CCTCTACAGT CATGAGGAGG
  GGAGGGCATT CCAAACAGAG GATGCTGCCA TCCAGTACTC CTGGATCCAA AAGATCTGGG
  AGGAAGGGAG TTGGGAGCAG GCAAGGTGGA TGGGGACTGT GAAGGTTTGT ATATGCTCAG
  CTCAGGAAGT GGCACTTAGG AGGTGTAGTC TTATTGGAGT GTGTGTGGCC TTGTTGGAGT
  R
  GGTGTGGACT TTAAGACCCT CATCCTAGCT GCCTGGAAGT GAGTCTTCTA CTAGTGGCCT
  TCAGATGAAG ATGTAGAACT CTCAGCTCCT CCTGCACCAT GACTACCTGG ATGCTTCCAT
  GTTCCCACCT TGATGATAAT GGACTGAACC TCTGAACCTG TAAGCCAGCC CTAATTAAAT
  GTTGCCCTTT ATAATTCTTG                                            
  
  R = A/G
  

  
  Note: Sequence in lower case indicates low-complexity or repetitive sequence

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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	MSM/Ms
ss149066696	ENSMUSSNP384550	ENSEMBL	ENSEMBL_Sanger	f	SNP	G	G	A
SNP Consensus Information
SNP					Consensus Type	A/J	DBA/2J	MSM/Ms
rs48535178					SNP	G	G	A