rs48122626 SNP Detail

Summary

• ID
  rs48122626
• 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:111861172 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              CAAAATGCAA ATGAGCTATC
  CATGATTCAT TATTCAGTAC CACACTCCAT GAAATGAGGA TAACAATAAG TGCCTACTAC
  TGCACTAGAT TTTTGTTGAG ATAAGTTTTT TTTTCTTAAC TACTGCAAAG TACTCACAAT
  GTCTGGCATG TAACGAATGC TTTAATATAT AATCTATCAC TTTTATTATC TAATATACCG
  R
  TACCATTTAA GAAACAAAAA TACCCTAAGT TTATCTCTTC AAATTTCCAA TTGTCAGTTA
  TAGACCTCTT TTTAGTCTAT CTCATTAGCT TCTGTAAAGG AATTTTAATC CAGCAACATG
  ACTGCTCTGA TCACATCCAA AGCCTTCTAG GTCTGTATGA TTTGGCTGAA ATGCAGACAC
  ATCAGTACCA CACAAATTTA                                            
  
  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	129X1/SvJ	A/J	DBA/2J	LG/J	SM/J
ss134277785	ENSMUSSNP7174912	ENSEMBL	ENSEMBL_Sanger	f	SNP	A	A	G
ss325913364	CHEV_X_110065084	CHEVERUD	SCREENING_POP	f	SNP				A	G
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J	LG/J	SM/J
rs48122626					SNP	A	A	G	A	G