rs231092257 SNP Detail

Summary

• ID
  rs231092257
• Variation Type
  SNP
• Alleles
  C

• 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
  Chr10:111274974 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TGAACTACAG TTCATTGTTT
  CTTTCAGAGT TAATGCTATG AATGGAGAAA CTGCAGGGAT CTTTAGATGG TGGCACAGGA
  ATTGTGCGGT ACTTGTTTTT AGTGCTGTAG GAAACCAGGC AGGTTGGTTT GAGGTAGACG
  TGTTTAGTGC AAGTGCCACA GTTAAAGGAG ACTCATATTA AATGATACTG TTTACTCATT
  C
  TGGAATTCTA GCCAGGCTGC TTGTCATTGG CATTACTGAT CGTCTCAATT ACACTTTAGA
  TCATTACTGG CATAACTGTG AACTTCATCC AAGCAGATTC TCAAGTCCAT AACATAGAGT
  TGAAAGTTCT CCAGCTCTTC ATGGATTCAT TTAGTTAACA GTATATGTGC AAATTAAGTT
  TCCCTGTATT CAAAGAGCCA                                            
  
  C = C
  

  
  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
ss323473593	CHEV_10_110876169	CHEVERUD	SCREENING_POP	f	SNP	C	C
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs231092257					SNP	C	C