rs107713115 SNP Detail

Summary

• ID
  rs107713115
• Variation Type
  SNP
• Alleles
  A/G

• Created in dbSNP Build
  132
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr9:97931667 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              GAAAGTAGAG TCTTAAAAGT
  AACATTTCAA TAGGAGAATA CAAAAAGAAA GGAAATAAAT AGAGTCTTCC CCCAGCAAAG
  AAAGAAAGTG ACAGACAACC TAGAGAACAG AGAACTGGAA CGGAAAACGG AGTTAGCATC
  TAGAGCATAT AACAGCAGGA AAAATAAATA CCAAATCAGC TGATTGCTAT GTAGGCAAAT
  R
  AACTGAACAA ATCATTCTCA AAGTAAGAGA AACAACCAGC CAATTAATAT AGGAAGAAAA
  GTTCCTCACC CAGCACCCTC GGAGAAATGC AAATTGAAAC CTAGGTTTCA TCCCAGTCTG
  AGTGGTTAGC ATCACGCCAA CAAATGGCAA ATGCTATTGA AGATTCGGGG TGAAAGTAAC
  CACATACACT GTTGAGCCAA                                            
  
  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	129X1/SvJ	A/J	DBA/2J	LG/J	MSM/Ms	SM/J
ss136836175	ENSMUSSNP2045283	ENSEMBL	ENSEMBL_Sanger	f	SNP	G	G	G		A
ss323125288	CHEV_9_97950033	CHEVERUD	SCREENING_POP	f	SNP				A		G
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J	LG/J	MSM/Ms	SM/J
rs107713115					SNP	G	G	G	A	A	G