rs213784892 SNP Detail

Summary

• ID
  rs213784892
• 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
  

Genome Location and Flanking Sequence

• Location
  Chr2:101296361 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                    TTTTAGCAC TTTACTTTTT CTTACAATTG
  AGGTGGCAAA AATTGCTGAG TCTTTGACAC TGGGAAAATT TTTATGAAGT AAGCACTTTA
  CTGTTTCAAG AGTAAATTTG Ggctgggcat ggtggtgcac acctttaatc ccagaagagg
  Y
  gggtagatgt caaaatgtca aaaccagcct gtacaaagaa agttcaagac tagccagagc
  tgttacaaaa gaaaacctca aaaaaataaT AAAAATAAAA ATGAGAAACa cagacagaca
  gacagataga tagacaggca gGAAAAGGAA                                 
  
  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
ss320428384	CHEV_2_101306173	CHEVERUD	SCREENING_POP	f	SNP	T	C
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs213784892					SNP	T	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:101296361 () rs orientation: forward

Symbol	Name	Function Class
Rr561501	regulatory region 561501	1192 bp distal