rs261939437 SNP Detail

Summary

• ID
  rs261939437
• 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
  Chr9:119183134 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              ATGTCTTTCC AGACTTTTCC
  TTCACGTGTG TGGATGTCCT AGCTTCGAAT GTGCACAGAA GGAGGCAAGC AGACCCCAAG
  GGATGAACAC AGTAAAATCA GAAAGAAGAT GAACATTTTA ACTGTCCTAA ACCAAATTTG
  CTTCTAAAGA GAGTACAAAC ACGCGGCAGG CTCGTCCCCT TTGGGGAAGA CTAACTCCTC
  Y
  CCCCGTAGAG CTGTTTGCTC CCACCCCACA TTCCGTCAAG CATTTCTCTA TCTGCAAACA
  TTAACTCTGC TTTTTAAAAA ACGCAATGTC AGCTGCCCTT TTAACAGAGG CTACTGATTT
  AACAGAAGGC AGGTCCAACC CCACCCTCCA AGGAGGACCA GGAGTTGACT GATGCTTGTC
  CTGATAGAAA CAGTTGGCCA                                            
  
  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
ss323218988	CHEV_9_119263186	CHEVERUD	SCREENING_POP	f	SNP	T	C
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs261939437					SNP	T	C