rs216007755 SNP Detail

Summary

• ID
  rs216007755
• 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
  Chr9:97934215 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TCGATCCGAT GATTTTAATA
  TTCGAGCTCA GAAGGAGAAA ATTGAATGTG ATATTGAATT TCCAGGGAAC TGATCATCTG
  AGTTTGATAT AAAAATGTCT GAGGAACAAC AACAACAACA AAAACAAGAA TAAATCCAAA
  TTAATTACGA GTTTTCAAAG TCTTGATGAC CTAATTTGAC AAAGACAGGA AGGCAAAAGC
  Y
  AAATTGCAGG GCCAGCCCAC CCATGAACAT AGCTGAAGTG CTCCATGTTC CGCTTCCCCT
  CAAAACAGTG ATCGAGCTCA CCAAACAGAG TATTGAAAAT TAGGGCTTGT TTCAGAAATG
  CAAAGTTCAT TTAATTTTAA GAAACAGAGT GATATAATTC ACTGTATTAA CATATTTAAA
  GGAATGAATG AATTATTAAT                                            
  
  Y = C/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
ss323125298	CHEV_9_97952581	CHEVERUD	SCREENING_POP	f	SNP	T	C
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs216007755					SNP	T	C