rs46069758 SNP Detail

Summary

• ID
  rs46069758
• Variation Type
  SNP
• Alleles
  C

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  132
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr3:143868917 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      G ATTGCTAAAG GATAAACTAA TATATTAAGG CTGCACATGT
  GTCTTGACAG TCTGTCAAAC AGACAATGCT CACTTTTTAA AGATGTTTGG CTTGCAAAAT
  C
  CCAGTTTCCA CACTGAAATA CTAATTAGCA ATCAGATGGG TAAGAACCCC TATTTTGAGA
  CAGTTCTTCA TGTGTTAAAG TTGCATCCTG CTAGTATTAC C                    
  
  C = C
  

  
  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
ss136029067	ENSMUSSNP4272230	ENSEMBL	ENSEMBL_Sanger	f	SNP	C
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ
rs46069758					SNP	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:143868917 () rs orientation: forward

Symbol	Name	Function Class
Gm34162	predicted gene, 34162	within coordinates
Rr586589	regulatory region 586589	1509 bp distal
Rr586590	regulatory region 586590	699 bp proximal
Rr586591	regulatory region 586591	1583 bp proximal