rs46768342 SNP Detail

Summary

• ID
  rs46768342
• 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
  Chr6:7829322 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TTTGCTGTTG TTCACTCCAT
  GGGTTTGGAG AGTTGTGTAG TGACACATAC ATGCATTATA GTATCATAAA GAATAGATTC
  TGTTCCAAAT CTCCTATATC CCTGCTTCCT ATTCATGCCA CCTTCCTTTC CAACTCCCAG
  CGACCTTTGG TCACTCTGGA TAGTCTTTTC TTTTCTAGAA AATCAGCTGG TTGTAATCAT
  R
  CAGCACATAG TCTTTTGAGA TGTTTTTTTT TTTTTTTTTT TTTTTTTTTT TCTTAGTAGC
  ATGCCTGGAA GACTCCATTG TATCTTTTAG TATCTTGGCA TTTTTTTTTT TTTTTTTACT
  GTTGAATAGC ATTTGTACTG ATACTGATAT CATTTCTCTG ACCAATTACC CAACAGGAAC
  AACCTAAGAA AGGAAAGGTT                                            
  
  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
ss132955681	ENSMUSSNP5004912	ENSEMBL	ENSEMBL_Sanger	f	SNP	A	G
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J
rs46768342					SNP	A	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr6:7829322 () rs orientation: forward

Symbol	Name	Function Class
Rr626323	regulatory region 626323	1526 bp proximal