rs250036024 SNP Detail

Summary

• ID
  rs250036024
• Variation Type
  SNP
• Alleles
  C/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
  Chr3:10155946 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                    taacagcag caaaattaca gtcataaaat
  accaatgaaa ataattttat ggttgggttc actacatcat gaggaactat ataaaagggt
  cccagcattg ggaagggcga gaaccaccgT CTTAGAGTAA GATGCTGAGA GCTGACAGTT
  Y
  TAAGGTGAAT GGCTCAACAG CTTAGGAAGC TGTTCTCGTG GAGTTGTGAT AGCTAAAGCA
  CATTTTTTAC TCAATGCAAT TAATATTTAG CATTTGAAGT GTACAATTTT CAGTATATGC
  TAATTTTTAT TCTCAACTCT TAAACCGTGC                                 
  
  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	LG/J	SM/J
ss320652922	CHEV_3_10090886	CHEVERUD	SCREENING_POP	f	SNP	T	C
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs250036024					SNP	T	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:10155946 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Gm37308	predicted gene, 37308			931 bp upstream
Myef2l	myelin expression factor 2 like			Intron
				Noncoding-Transcript-Variant
Rr573569	regulatory region 573569			1654 bp proximal