rs33494292 SNP Detail

Summary

• ID
  rs33494292
• Variation Type
  SNP
• Alleles
  G/T

• Created in dbSNP Build
  125
• Last Updated in dbSNP Build
  138
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr2:122270641 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                        AAGAT CATATCAAAT GCAAGAGATC
  K
  GCACTGTGAC TAAAGCCAAT GGGAA                                      
  
  K = G/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	129S1/SvImJ	129X1/SvJ	A/J	C57BL/6J	DBA/2J	LG/J	SM/J
ss45285249	mCV22597798	ABI	CRAMUS_MOUSE	f	SNP	T	T	T	G	T
ss147419452	ENSMUSSNP3793479	ENSEMBL	ENSEMBL_Sanger	f	SNP			T		T
ss320488791	CHEV_2_122265896	CHEVERUD	SCREENING_POP	f	SNP						G	T
SNP Consensus Information
SNP					Consensus Type	129S1/SvImJ	129X1/SvJ	A/J	C57BL/6J	DBA/2J	LG/J	SM/J
rs33494292					SNP	T	T	T	G	T	G	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:122270641 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Rr563981	regulatory region 563981			441 bp proximal
Slc28a2	solute carrier family 28 (sodium-coupled nucleoside transporter), member 2			Intron
				mRNA-UTR
				Noncoding-Transcript-Variant