rs224185062 SNP Detail

Summary

• ID
  rs224185062
• Variation Type
  SNP
• Alleles
  A/C

• 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
  Chr13:5678495 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              GCCAACAATG CTATTGCTCA
  GTATATCCTT TCTTCCACAC TCTCGTGGTC CCAACCACTT TCCCACTCCA CCCAAACACT
  ACTTCTTTAG CACAGTACTC ACAAAGATAG GAAGTGTTTG TCCTCATCAC TCAGACATCT
  ATTTTTAAAC TTGGGATTTT TCCAAGCCTT CCTACTTCTT TGGTGATAAT ATTCCAAATA
  M
  ATCTGTTCTT TCTTAATGGA ATGTGATTTG GTAAAATTTA AGCAACATGA AATAACCTTG
  ACTAAAAACT AAATGAATTT ACTGTTTTCC AAAATGCACC ATTTCATTAG TTTTAAGCTA
  TTTAGATATC TGAAGTTTTC TTGTGCTTTT ATTTCAGGCT GATTAGCTTT AGCGATGACT
  GTTATTTTTA GTAAAAGAAG                                            
  
  M = A/C
  

  
  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
ss324222376	CHEV_13_5627742	CHEVERUD	SCREENING_POP	f	SNP	C	A
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs224185062					SNP	C	A