rs50802095 SNP Detail

Summary

• ID
  rs50802095
• Variation Type
  SNP
• Alleles
  G/T

• 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
  Chr3:123600893 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              AGGCTCATAT ATTTTAATGC
  TTAGTCTTCA GGGAGTGGCA CTAGTTGAGA GGGATCAGGA GGTGTGGCCA TACTGGAGGA
  AATCTGTCAC TGGGGGTGGG CTTTGAGGTT TTGGAAACTC AAGTCAGGCC CCGTGTCTTA
  CCCTTCCTCC TGCCTGTAGA TCCAGATGTA GAACTCGGCT ACTTCTTTAG CACCATTTCT
  K
  CCTGTCTGTT GCCATTCTTT CCAGCAGGAT GAGAAGGACT AAACCTCTTA ACCTATAAGC
  CATCCCCAAA TAAATGTTTT CTTTTATGAG CTGCCATTGT TATTATGTCT CTTCACAGCA
  ACAGTATACT GGCTAAGGCA TAGTTTTACT AATTTTTACT TTAGTAAGTA ATATTAGACT
  TTCATTAATT GAGTCATAAA                                            
  
  K = G/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	129X1/SvJ	A/J	DBA/2J	LG/J	SM/J
ss135773716	ENSMUSSNP7188576	ENSEMBL	ENSEMBL_Sanger	f	SNP	G	G	T
ss320923137	CHEV_3_123510162	CHEVERUD	SCREENING_POP	f	SNP				T	G
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J	LG/J	SM/J
rs50802095					SNP	G	G	T	T	G