rs219929882 SNP Detail

Summary

• ID
  rs219929882
• Variation Type
  SNP
• Alleles
  C/T

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

Genome Location and Flanking Sequence

• Location
  Chr3:109931749 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                    GGTTATAAG GAAATCTTAT CCAGGACTAA
  GAGGGGCACC AACGTTGGCT ACTTGATCAG TATCTCTCTA CCTCCCAGAG AAGCTCATAT
  CCAGTGAAGA GTTGGGTTTT TTTTGTTTGG TGGTTTTTTT TTtttttttt ttttgagaca
  Y
  ggtttctctg tatagccctg gctgtcctgg aactcagaaa tcccctcccg agtgctggga
  ttaaaggcgt gtgccaccac gcccggttTA GGAGTTGATG CAGGAATCTT AACATCTGCT
  GTCCCTCTTG CTTGGGTTCT GGCATGGCTA                                 
  
  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	LG/J	SM/J
ss320871329	CHEV_3_109827351	CHEVERUD	SCREENING_POP	f	SNP	C	T
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs219929882					SNP	C	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:109931749 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Ntng1	netrin G1			Intron
				Noncoding-Transcript-Variant
Rr583457	regulatory region 583457			1213 bp distal