rs226661163 SNP Detail

Summary

• ID
  rs226661163
• 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
  

Genome Location and Flanking Sequence

• Location
  Chr13:114659465 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                    TCCAAGCAG AAGGAGGGGA GAGATTTGGA
  TTTACTGAGG AGTTCCCCAT GAACGTATGT GGGTAGAAAA GTAGATAGTC TCTTTTCCTT
  TAACACAGAG TTCCGGTGAG AAAGGACTGG GAGAGATAAA TATGCCGGGT GGGATTATCA
  R
  TCAGCTCAGA ACAAAGTTAC ACAAGGCTTC TCCCTCCTGA CTGCTTCTCA ACTGGAGGGG
  AGGATGTCAG AAACGTGACA AGCCACACAA TACTAGTTTG TAAAGGATGT GATATCAGTC
  AGTGGTAATA TTTCCTATAA AAATATCAAT                                 
  
  R = A/G
  

  
  Note: Sequence in lower case indicates low-complexity or repetitive sequence

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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
ss324534046	CHEV_13_115313137	CHEVERUD	SCREENING_POP	f	SNP	G	A
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs226661163					SNP	G	A