rs29755886 SNP Detail

Summary

• ID
  rs29755886
• Variation Type
  SNP
• Alleles
  C/T

• Created in dbSNP Build
  125
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr17:84413336 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        CCATGAGGGT ATGTCTCCCT CACAGGATAG GGCCTGTGTC
  CTTATGCCCA GAGTCTTAGT CTGTGTCCAA CACACAGCAG AACCTACATG AGAAAGAACA
  Y
  AGGTATCTGA AGACTAGAGC TGAACTCTAA GACATTATGG TCCCCCAAAA AAATTGCCGT
  GGAGCTCATA ACACAGATAG TTCTTGGCTT AGGAATTTT                       
  
  Y = C/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	MOLF/EiJ	WSB/EiJ
ss48383782	NES12277781	PERLEGEN	MM_PANEL2	f	SNP	C	T
SNP Consensus Information
SNP					Consensus Type	MOLF/EiJ	WSB/EiJ
rs29755886					SNP	C	T

Additional submitted assays for this SNP, where the strain of origin for observed alleles is not specified by the submitter

Assay ID	Submitter SNP ID	Submitter Handle	Population	ss orientation	Variation Type	Alleles
ss48383782	NES12277781	PERLEGEN	MM_PANEL	f	SNP	C/T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr17:84413336 () rs orientation: forward

Symbol	Name	Function Class
Rr531986	regulatory region 531986	1251 bp distal
Tssr149629	transcription start site region 149629	495 bp downstream