rs264150392 SNP Detail

Summary

• ID
  rs264150392
• Variation Type
  SNP
• Alleles
  T

• 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
  Chr4:103044888 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                    GACTTTCTT ATTGTTTGAG TGGAAAGACA
  AAATTAAGCA TAAAGTAAAC AAGGGTATCA GGTATCTTAG AAAGGAATGG GATAGGACCT
  CTCATTGGAT GAAGCGACTG ATATGCATAG TGTGCACAGG GGACAGGAGG GGACAGAGGA
  T
  CCAACCCTCA CTGCTCACAA CCACAAATTA GGAAACAAAC AAGGACACAG TAAAGTATGT
  TAAGCAATCT CTTCCCCACA GAAATGACCG GGAAGTACCA AAAAGCATCA TATTAACTCA
  AAGCTAAGAC TGCAACTCCC AATTTGTATG                                 
  
  T = 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	LG/J	SM/J
ss321236076	CHEV_4_102860296	CHEVERUD	SCREENING_POP	f	SNP	T	T
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs264150392					SNP	T	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:103044888 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Rr596372	regulatory region 596372			1275 bp proximal
Slc35d1	solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1			Intron
				Noncoding-Transcript-Variant