rs48421027 SNP Detail

Summary

• ID
  rs48421027
• 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:111860364 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              CAAAATAAAA ATCATATTCA
  ATGCATTTTA AAGTTTTCTT CATAATTTTA TACCTCTACT CTTGATATCT TTGTCTTTGT
  TTGATATTTG ACTACTAAAA GTTATTTTTA TTTAAGAATG TGTAATAGAG ATGGTAAAGG
  ATTGCGTTTC CGTGTTAAAG GAAACCTATC CTGTCCAAAC CTCACCCACA AAGGCATTGC
  R
  AGTTTCTATC TTTCTGGGGT TTACCTTTGT CTGACCTTGG CTCCTTGCTT TCTGCTCTAT
  TGGGGACAAT GGCAGGTGAG AAGTCGGGTG ATTGATATAT GGGAAAAAGC AAATGCAAAC
  TGCCCACACT GGGATTGTTC TTTGTCAACA CACATAGTTG GCTGTAAATG CAGTATTTCC
  ATTAACACCA TATGTTAGAC                                            
  
  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	A/J	LG/J	SM/J
ss134277737	ENSMUSSNP407321	ENSEMBL	ENSEMBL_Sanger	f	SNP	G
ss325913352	CHEV_X_110064276	CHEVERUD	SCREENING_POP	f	SNP		G	A
SNP Consensus Information
SNP					Consensus Type	A/J	LG/J	SM/J
rs48421027					SNP	G	G	A