rs48373250 SNP Detail

Summary

• ID
  rs48373250
• 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
  ChrX:111860815 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              GGAAGCTAGT GAGCAGAATC
  ACTGTATTTA GTGGGTCCCA TATAAAGATG AAACCATATT TCCTTCACCA ACTTCATTTT
  TAAAAAAATG GTGCCCTGAC CTTCAAAAAA AGGCTTACTT TCACCCACTT CAGCAAAGAC
  TAGCTTGTAA ACCAAGACAT TGGCTCATTA CTATATATAA TGATAGCTAC ACTTCACAAA
  Y
  AGAGCACAAT CATTTATCGA TCCAACCCAC TCTCTCCTTG CTGGCAAATC AAAACATGAT
  CAGAAGTTTG TTTGGCAAGT TCAGACAAAA TAGAATGATC TGTGTGATTT GGCTGACTAG
  TAATCTCAAA AGCTGTGTCT ACACTTTGCC AGATCACAAA ATGCAAATGA GCTATCCATG
  ATTCATTATT CAGTACCACA                                            
  
  Y = C/T
  

  
  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	129X1/SvJ	LG/J	SM/J
ss134277761	ENSMUSSNP5923409	ENSEMBL	ENSEMBL_Sanger	f	SNP	C
ss325913356	CHEV_X_110064727	CHEVERUD	SCREENING_POP	f	SNP		C	T
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	LG/J	SM/J
rs48373250					SNP	C	C	T