rs238968169 SNP Detail

Summary

• ID
  rs238968169
• 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
  Chr9:119184369 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              AATCAATCAA TCGATCAGTG
  TAAAGACAAA AACTGAAATA AACCGGACTC TGCTTTATAT TGGCTGGTCC TGAGATTCTT
  TTCTGTGTTA GAGCCAGGAG TTCCAGTTGG CCGGAGTTGA AGTAACTAAG AGGTGAGGGG
  GAGCTGCCCA GGCTACGGTG GATGTTGGGG TGAAGCTGTG CTTTCTTCCT TGTACCCCTC
  R
  ATAGCACATC TCTACGGACA TGGCGCACAG AAGAGGCCAC CATTTGCACA TCTGAAAAGA
  GCCCTTACTG GGAGCTGACT GTCAGCACTA TATAGCTTTA GACTTTCCAG CTTCCAGAGC
  TGTGAGAAAC TGTTTAGCCC TTGGCATTGG TTTAGCAACA TGAGTGACAC ATAGTAAGGT
  CCTTGGGGGT CCCACTGGCT                                            
  
  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
ss323219004	CHEV_9_119264421	CHEVERUD	SCREENING_POP	f	SNP	A	G
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs238968169					SNP	A	G