rs46880078 SNP Detail

Summary

• ID
  rs46880078
• Variation Type
  SNP
• Alleles
  C/T

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr4:141446579 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TTAACAATGC GAGTCACCAT
  GCTCAGCACC CCAACAAAAA CCTGAGACAG GTTCTTACCG CGCAGGCTCA GCTGTCCTGA
  GACCTGAAAT GGAGTCCAGG CTGGCCTTGA ACTCTCAGTC TCAAATATCA AACAAAAACA
  ATCAAAACCA AACTAACACT CAATGTGCAA GTTATCCCTG GGTTATGAGG AATAAGTGAG
  Y
  TGTGGCAGTC TTTATCCTTC TCTGTGTTAC AACCTTTCTA GCATAGCTAT TCAGCATTTA
  CCAGAAAGAA AGAAAGAAAG AAAGAAAGAA AGAAAGAAAG AAAGAAAGAA AGAAACCAAA
  AAAACAAAAA ACAGGAAAGA AAAATACATA AGGAAATAAA CACATCAAAA CTAGCCACCA
  CAGAAACTTC CACTTTCCAT                                            
  
  Y = C/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	129X1/SvJ	DBA/2J
ss147742656	ENSMUSSNP6947148	ENSEMBL	ENSEMBL_Sanger	f	SNP	T	C
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	DBA/2J
rs46880078					SNP	T	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:141446579 () rs orientation: forward

Symbol	Name	Function Class
Ddi2	DNA-damage inducible protein 2	Intron
Rr398662	regulatory region 398662	19 bp upstream
Rr603862	regulatory region 603862	826 bp proximal
Rr603863	regulatory region 603863	1454 bp proximal