rs48104758 SNP Detail

Summary

• ID
  rs48104758
• 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
  ChrX:111860705 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TTTGTCAACA CACATAGTTG
  GCTGTAAATG CAGTATTTCC ATTAACACCA TATGTTAGAC AATTAATTGT ATCTATTGGA
  TCAAAGTCTT AGTTTCTTCT TACCTACTGT GGAAGCTAGT GAGCAGAATC ACTGTATTTA
  GTGGGTCCCA TATAAAGATG AAACCATATT TCCTTCACCA ACTTCATTTT TAAAAAAATG
  R
  TGCCCTGACC TTCAAAAAAA GGCTTACTTT CACCCACTTC AGCAAAGACT AGCTTGTAAA
  CCAAGACATT GGCTCATTAC TATATATAAT GATAGCTACA CTTCACAAAT AGAGCACAAT
  CATTTATCGA TCCAACCCAC TCTCTCCTTG CTGGCAAATC AAAACATGAT CAGAAGTTTG
  TTTGGCAAGT TCAGACAAAA                                            
  
  R = A/G
  

  
  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	LG/J	SM/J
ss134277754	ENSMUSSNP1924687	ENSEMBL	ENSEMBL_Sanger	f	SNP	A
ss325913354	CHEV_X_110064617	CHEVERUD	SCREENING_POP	f	SNP		A	G
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	LG/J	SM/J
rs48104758					SNP	A	A	G