rs237186417 SNP Detail

Summary

• ID
  rs237186417
• Variation Type
  SNP
• Alleles
  C

• 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
  Chr4:103044603 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                    ACCTCCCCA CTTCCTCCCC TTCTTGAGCT
  GTGACTGTCA CGTTCTTAGA CCCTGGACTC TCCTCCGTGA GCCTGTGAGA CAAAACTGAG
  GTTCAAGGCC Aggcctgggg tgcagctcag tgctagagca cttgcctggc atgtgcagac
  C
  cctggatttg atctgtagca TAAGGGTGGG TATAAAACGC ATTAAACCAA CCTTAAAACT
  GTCTCTGTAA TGAAATGCCC TTTGGGAGGG GATTCAGAAA TAATCAGCAC TTTCTAATGT
  TGGTCACATA GAGCAGACTT TCTTATTGTT                                 
  
  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	LG/J	SM/J
ss321236072	CHEV_4_102860011	CHEVERUD	SCREENING_POP	f	SNP	C	C
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs237186417					SNP	C	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:103044603 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Rr596372	regulatory region 596372			1560 bp proximal
Slc35d1	solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1			Intron
				Noncoding-Transcript-Variant