rs213447112 SNP Detail

Summary

• ID
  rs213447112
• 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
  Chr13:114660238 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                    ACGATGTGG AGAATCTGGG GCAATCATGA
  GGGGGTATTT GCTGTTCTTT ATCTCCTTGC TTCCAGAACC TCTAGCTTAG GGAGGTATTT
  TTTCTCACAT TCTCCAGAGT TCAAAGAGTT TATGGGACAA CAGAAACCTA ATATTTGTTC
  Y
  CGTCTTTCCA TTATATACCA CACCAGAACA CACTTTTTTT TTCTTCACAC AACAGTTAAT
  TAGATTTCCC GGAAGCGGAA GAGCCATTTG CTTTTCGATG GCTTTACTAT CAGTCTGCAA
  ACCCAGAACC TTTCCAATGG TTTAATACAA                                 
  
  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
ss324534048	CHEV_13_115313910	CHEVERUD	SCREENING_POP	f	SNP	C	T
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs213447112					SNP	C	T