rs239578470 SNP Detail

Summary

• ID
  rs239578470
• Variation Type
  SNP
• Alleles
  A/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
  Chr9:78755300 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                    GCACCGTGT TTGGGCAAAT CTTGAGATAT
  TAGTTTAGTG CAATATTAAG AAACTTTAAA AAGCAGTAAT ATGGATATAC CTTTTCATAT
  TTAATTTCTG CTCAGCATAG AAATGTCCCA ACATGTTAAC AAAACAGACG GAAGGCTGTG
  W
  CTGCTTTTTA CTTTGATCTT GGAGGCCATA TGTGCATCTG TGTGTGGACA CAGCCTGTGA
  GCTGTGGGTG ACTGTGAAGC ACGGTTCTCA ATGATGGCTT CTGTGTGACA GAATTAGAGA
  TTTTTCAAGG TACTTAGTCA TGCTTTGCAT                                 
  
  W = A/T
  

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

  ---

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
ss323017422	CHEV_9_78695825	CHEVERUD	SCREENING_POP	f	SNP	T	A
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs239578470					SNP	T	A