rs257788306 SNP Detail

Summary

• ID
  rs257788306
• Variation Type
  SNP
• Alleles
  C/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
  Chr9:119183978 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              ACAATACTGG GATTTATAGC
  CTTGTCCCTG CTAGGCAAGT GCTCTATGGC TGAGCTGCTC TCCCAGCCTG CATTTTATAT
  TCAGATGGAC CACTAAACTG CTCAGGCTGG GCTTGAACTC ACTACAGATG TGGGTACTGG
  GAATCAAACC CAGCTCTCCT GCAAGACCAG TATGTGCTCG TAGCCACAGG GCCATCTCTC
  S
  AGCCCCTCTT CTGTGCAGCC TTTCTCTCAG CCTTTGTGCC ATCAAGATGG CTCAGTGGGT
  AAGGACCCTG GCTGGCAAGC CGTATGATCC GAGTTTGATC CCCAGAATTC CCATGGTAGA
  AGGGAGACCC TATTTCTTCA CATTGTTTGG CAGCTACACA CATGACACCA TGCACACCAT
  ATCAATGATC AATCAATCAA                                            
  
  S = C/G
  

  
  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
ss323218997	CHEV_9_119264030	CHEVERUD	SCREENING_POP	f	SNP	C	G
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs257788306					SNP	C	G