rs248990599 SNP Detail

Summary

• ID
  rs248990599
• Variation Type
  SNP
• Alleles
  A/G

• 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
  Chr13:58638954 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              ACCATCAAGA AGACAAAGGA
  CAGCCAGTAT CGTCAGTGTG GGGAAAGTGT TAGAGGGAGC AGAAGCTGGT GTAGCCATTT
  TGGAAACCAG CCCAGAGGCT TCTCAAGAAG CTTGGAAGTG CTGTGTGATC CCTCGACGAC
  GCTTCCCCTG AGCTCACACC CCCAAGGCTC CTGCCCATGC CGAGACACTT AACACACCCA
  R
  TGCTCATTGC TGTTCTGTTC ACAACAGCCA GGAAATGCAC ACAGCCCCGG GAAAATAATT
  TAATCCGATC ATTGTCAAAA CATTTCCCGA ATGTATCCCG GTGCACTCCC AGAGGAGTAC
  AGATTCTTCG TCACCTCACA GTGATGTCCT TTGGGTGTCA CCAGGCTTAC GAGCGTACGT
  TTCCGTCACG GATGGGGGTG                                            
  
  R = A/G
  

  
  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
ss324353807	CHEV_13_58592501	CHEVERUD	SCREENING_POP	f	SNP	G	A
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs248990599					SNP	G	A