rs48150535 SNP Detail

Summary

• ID
  rs48150535
• Variation Type
  SNP
• Alleles
  A

• 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
  ChrX:111860479 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              GAATGTGTAA TAGAGATGGT
  AAAGGATTGC GTTTCCGTGT TAAAGGAAAC CTATCCTGTC CAAACCTCAC CCACAAAGGC
  ATTGCAAGTT TCTATCTTTC TGGGGTTTAC CTTTGTCTGA CCTTGGCTCC TTGCTTTCTG
  CTCTATTGGG GACAATGGCA GGTGAGAAGT CGGGTGATTG ATATATGGGA AAAAGCAAAT
  A
  CAAACTGCCC ACACTGGGAT TGTTCTTTGT CAACACACAT AGTTGGCTGT AAATGCAGTA
  TTTCCATTAA CACCATATGT TAGACAATTA ATTGTATCTA TTGGATCAAA GTCTTAGTTT
  CTTCTTACCT ACTGTGGAAG CTAGTGAGCA GAATCACTGT ATTTAGTGGG TCCCATATAA
  AGATGAAACC ATATTTCCTT                                            
  
  A = A
  

  
  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
ss134277752	ENSMUSSNP4474198	ENSEMBL	ENSEMBL_Sanger	f	SNP	A
SNP Consensus Information
SNP					Consensus Type	A/J
rs48150535					SNP	A