rs51006118 SNP Detail

Summary

• ID
  rs51006118
• Variation Type
  SNP
• Alleles
  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:74801825 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        GGGAGCCCCC AGTCCCTCCT TGGCTGCCAG GAAAAGAGCG
  GGTCGGCCGC CATGTTCAGA GAGGCGCAGG GATGTGCAGG CGGAAACCTC AAACCAATTC
  T
  GCTTGATGGC AGTAAAACAC CGCGAATGGC AACTGCCAGG CTGCTGGGCG CTCTCCCTCT
  GCCCTTCTAG AGGCAAAAAA CGCCAACCTG CAACCACCA                       
  
  T = T
  

  
  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	DBA/2J
ss134210184	ENSMUSSNP6346403	ENSEMBL	ENSEMBL_Sanger	f	SNP	T
SNP Consensus Information
SNP					Consensus Type	DBA/2J
rs51006118					SNP	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: ChrX:74801825 () rs orientation: forward

Symbol	Name	Function Class
4933407K13Rik	RIKEN cDNA 4933407K13 gene	within coordinates
Gm61855	predicted gene, 61855	1841 bp upstream
Rr4698	regulatory region 4698	176 bp proximal
Rr4699	regulatory region 4699	976 bp proximal
Rr8776	regulatory region 8776	24 bp distal
Rr8777	regulatory region 8777	775 bp proximal