rs234756438 SNP Detail

Summary

• ID
  rs234756438
• Variation Type
  SNP
• Alleles
  A/T

• 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
  Chr12:17730132 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              CTTATGCCCA TTTAACCAGT
  GTCTCAGGAT ACAGAATGTC TCCATCATGC CCCAAATTTC CTAGCATCCT TTGCAGTCAG
  TCATTCACTA CTCCCAACAC ACTTATCAGC CCTAGATAAC AACCATCAGC CTACTTCCTG
  TCTTACAGAG TCATTTCAAC CTGAGCTACT TTTAATATAT CTTATATTAT TTTATTATGC
  W
  TATATACACA TGTATATATA TACATATACA ATATACATAT GTACATATAA ACAACATATG
  TGCATATACA TTATATATAT GCATTATATG TACATATATA CACATATACA TATATACGTA
  TGTATAGGTG TGTATACATA TGAGTATGGA TGCCTGCAGA GTCCAGAAGA GAAGATCAGA
  TCTCTGGAAG CTGGAGTTAT                                            
  
  W = A/T
  

  
  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
ss323926900	CHEV_12_17686937	CHEVERUD	SCREENING_POP	f	SNP	A	T
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs234756438					SNP	A	T