rs213088203 SNP Detail

Summary

• ID
  rs213088203
• 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
  Chr4:129185196 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                    TTTGATTAT CTTCATCTGA ATGTGAATGA
  TGGAGAAAAG CTATTCAGCA AGATTCGCAA CATTAGTGTT TGGAGTCCAT ACGCATAGAT
  TGTATGTGTG CACACACATA TGATtctgta cacatacaga ctgattctga actctctctg
  Y
  tggtgagaat gacccggaac ctctgattct cctgcctcta cctcctgagt gttgaggtta
  caggaatagg cgcgtactat cTACCACAGC AGGttttatg tggtgctagg gatcaaggcc
  aagacctccg acatgttcca tgagcactct                                 
  
  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
ss321311648	CHEV_4_128968647	CHEVERUD	SCREENING_POP	f	SNP	C	T
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs213088203					SNP	C	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:129185196 () rs orientation: forward

Symbol	Name	Function Class
Sync	syncoilin	Intron