rs260202333 SNP Detail

Summary

• ID
  rs260202333
• Variation Type
  SNP
• Alleles
  G

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

Genome Location and Flanking Sequence

• Location
  Chr4:103045336 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                    AGATCCTTA CGTGGAAGCT TAAGACAACT
  TAGGAAAATG ACGGCTGATC TCTGAAAGCT GTGATCAACA CTATTTCATC AGAAGGTCCG
  CTGTGGCTCC CAAGACTGTG GCCAGCCATG GTAGGAAAAT TCTCATACTT TACTTGTAAG
  G
  CCACACAGCA GACAGTAGCA AAAACAACAG TGAACTAACC AATCATTTAC TCCTCCCTTG
  AGCTTAAAAT GAAACCGACA GAAGGTAGGT GTGATGGGAA GCACAGATGG CCATGTGATC
  ACGGGGCATG GGTACCCTTG GCTGACCATG                                 
  
  G = 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	LG/J	SM/J
ss321236084	CHEV_4_102860744	CHEVERUD	SCREENING_POP	f	SNP	G	G
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs260202333					SNP	G	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:103045336 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Rr596372	regulatory region 596372			827 bp proximal
Slc35d1	solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1			Intron
				Noncoding-Transcript-Variant