rs261374331 SNP Detail

Summary

• ID
  rs261374331
• 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
  Chr9:119184259 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              CGTATGATCC GAGTTTGATC
  CCCAGAATTC CCATGGTAGA AGGGAGACCC TATTTCTTCA CATTGTTTGG CAGCTACACA
  CATGACACCA TGCACACCAT ATCAATGATC AATCAATCAA TCGATCAGTG TAAAGACAAA
  AACTGAAATA AACCGGACTC TGCTTTATAT TGGCTGGTCC TGAGATTCTT TTCTGTGTTA
  R
  AGCCAGGAGT TCCAGTTGGC CGGAGTTGAA GTAACTAAGA GGTGAGGGGG AGCTGCCCAG
  GCTACGGTGG ATGTTGGGGT GAAGCTGTGC TTTCTTCCTT GTACCCCTCG ATAGCACATC
  TCTACGGACA TGGCGCACAG AAGAGGCCAC CATTTGCACA TCTGAAAAGA GCCCTTACTG
  GGAGCTGACT GTCAGCACTA                                            
  
  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
ss323219000	CHEV_9_119264311	CHEVERUD	SCREENING_POP	f	SNP	A	G
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs261374331					SNP	A	G