rs246629583 SNP Detail

Summary

• ID
  rs246629583
• 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
  Chr13:114659164 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              GCCTAGTTGA CCATCAATGG
  GAAGAGTGGC CCTTTGGTAT TGCAAACTTT ATATGCCTCA GTACAGGGGA ATGCTAGGGC
  CAAGAAGTGG GAGTGGGTGG GTAGGGGAGT CGGGGGTAGG GTATAGCGGA ATTTTGGGAT
  AGCATTTGAA ATGTAAATGA AGAAAATACT TAATAAAATA TATTAAAAAA AATCTCAGTG
  Y
  TGTAGTTTAT TAAGAGGAAC TAGAGAGACC AGACTGTGCT AGCGAGACAG GACATGCCCT
  GTTTCTGTGA AGGACTGAGG TTTGTGTATC TTTTAAATGA TAAAACTCAA CTTACTTGAA
  AAGAAAAGAA AAACCCAGTG ATAATTGATT CTCCAAGCAG AAGGAGGGGA GAGATTTGGA
  TTTACTGAGG AGTTCCCCAT                                            
  
  Y = C/T
  

  
  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
ss324534044	CHEV_13_115312836	CHEVERUD	SCREENING_POP	f	SNP	T	C
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs246629583					SNP	T	C