rs49280490 SNP Detail

Summary

• ID
  rs49280490
• Variation Type
  SNP
• Alleles
  A/C

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr9:42068739 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        AATTTATAGG TATGACCAAC ATGGGAATTT CACTGTCTGG
  CTTACTTGTT ATGAGTTATA CTTTTTAAAG TGCTAACTTA TATGACAAAT CTAGGAGGCT
  M
  TGTTGGCTAG CACAATTTAT TTTATTGAAG TAAGAGGTGG TGTTTTCCCT AATGCTTTAG
  GCAAGCTCAC TGACCTGTAT AAACCCTTCT AATATTGTT                       
  
  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	129X1/SvJ	A/J	LG/J	SM/J
ss136376450	ENSMUSSNP4106948	ENSEMBL	ENSEMBL_Sanger	f	SNP	A	C
ss322933009	CHEV_9_41965526	CHEVERUD	SCREENING_POP	f	SNP			A	C
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	LG/J	SM/J
rs49280490					SNP	A	C	A	C