rs264948408 SNP Detail

Summary

• ID
  rs264948408
• 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
  Chr9:119181938 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              GGGATTACAG GCTCGTGCCT
  CCACCCCTCC TGAAGCCTAT TATTATTATT ATATTATTAT AAATTATTAT TTTGTTTTGT
  TTTTGAGACA GGGTTTCTCT GTGTAATAGA GCCCAGCTAT CCTGAATCTT GCTTTGTAGA
  CCAGGCTGGC CTAGAACTCA CAGAGATATC CCAAGTGCTA GAATTAAAGG CATGTGCCAC
  Y
  GTGCCTGACA AAACCAGTAA TTATTAAATA GAGGATAAAT TTAAGCCAGG CACTGGTATA
  TGCCTGTAAG CCCAACACCT GCAAAGGGAA GTGGAGGCAG GAGAGTTCAT TCTCTTGAGA
  ACGTAGGAGT TTGAGGCAAG CCTGAGTTTC AAGAGATTCT CTGGAAGACA CCTAGGAAAC
  ACACATACAC ACTGGGATTC                                            
  
  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
ss323218977	CHEV_9_119261990	CHEVERUD	SCREENING_POP	f	SNP	C	T
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs264948408					SNP	C	T