rs261297356 SNP Detail

Summary

• ID
  rs261297356
• 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
  Chr1:132884573 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                    TTTAGAGAA GATACTTTCA ACCCAGTCCA
  ACCTGCCTCT GTCACTGGCC TACTGTAAGG ATCTGTTTCT GTGTCCTCAA CTCAACACAG
  AACTATACAT GTTCTGAAGA CTTCCTACCC CACCAATCCT GAATCTACAG AACTACCATA
  R
  CTTCCTATCC CCTGCTGGCC TCCTGAAGTT AGCGTAACTG AAGTTCAGCG CTGGGAGGCT
  GCCCTCTGGA TCCGAGCCCT CTACTCCATT TGGAAGAAAC GACATCCTGG CTGTTTATGT
  GGTACTGGGA GAGGGAGCAC TGAAGAGAAT                                 
  
  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
ss319978137	CHEV_1_134853412	CHEVERUD	SCREENING_POP	f	SNP	A	G
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs261297356					SNP	A	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr1:132884573 () rs orientation: forward

Symbol	Name	Function Class
Rr19288	regulatory region 19288	1228 bp proximal
Tssr8757	transcription start site region 8757	1215 bp upstream