rs266208675 SNP Detail

Summary

• ID
  rs266208675
• Variation Type
  SNP
• Alleles
  A/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
  Chr4:104454575 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                    gagtctacc ctatttCACT GAGCCGTTCG
  GCGCTGCACG ATACCTCTAT AAGGGTTATG AGTCCAGAAC ACAGAAATGA ATAGTCACCT
  GGAGCGTGCT GGCATTGGCC TGCTTTAGAC TTGGGAATAC TGTAACTAGG GGGAAAAAAT
  R
  AGAAGCATTC ACAACTGCAC AGACCACACT AGGGAAAAAA GAGGTCTCAG CTTAGTGTAA
  GTTGGTGTGG CCACTCATCA TATATTCTGA GGCAATGTAG GAGCTACAGA AACAATAATC
  TTGAGTGTGA AATATCTTTT ATTTGGCCAT                                 
  
  R = A/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
ss321241243	CHEV_4_104269983	CHEVERUD	SCREENING_POP	f	SNP	G	A
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs266208675					SNP	G	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:104454575 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Dab1	disabled 1			Intron
				Noncoding-Transcript-Variant
Rr596483	regulatory region 596483			138 bp proximal
Rr596484	regulatory region 596484			685 bp proximal