rs48651006 SNP Detail

Summary

• ID
  rs48651006
• 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
  Chr1:189725195 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        TTTGTTTGGA CTCAGGATCT CTCTCACTAT GCAGCTCAGG
  CTGTCCTGGA ACTCACTATA TAGACCAGGC TGACCTCAAA CTTACCTGGC TCTGTGCCAG
  R
  ATTAAAGGTG TGCACTGCTA TTCCTGAAAA ATAAGGACTT TAAAAAAATT AAAAAGAAGG
  AGAAATGGTA ATACCTGATT TGGCGTACAG TTCCTGTAT                       
  
  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	A/J	DBA/2J
ss146493609	ENSMUSSNP1429155	ENSEMBL	ENSEMBL_Sanger	f	SNP	A	A	G
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J
rs48651006					SNP	A	A	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr1:189725195 () rs orientation: forward

Symbol	Name	Function Class
Gm70453	predicted gene, 70453	482 bp upstream