rs52119391 SNP Detail

Summary

• ID
  rs52119391
• Variation Type
  SNP
• Alleles
  G

• Created in dbSNP Build
  128
• Last Updated in dbSNP Build
  132
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr2:180851093 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      G AGGATAGGGA GGAAAGAGGA AAGGAGGGAA GCAGGGAGGG
  AGGGAAAGAA GAAGGAAGAG AGGGAGGGAA GAATGAAGGA AAAAAGGGGG AAGGGAAGGA
  G
  GGAAGGAAGG GAGGAAGGGA GGGTACTTAA TAACTAGCAT GTCTATATGA AAGGCTGCTA
  GTGTGGGAAT CAACTGCCCC AAGGCCTGGG ACAGATGAGC A                    
  
  G = 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	129X1/SvJ	A/J
ss148398749	ENSMUSSNP316464	ENSEMBL	ENSEMBL_Sanger	f	SNP	G	G
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J
rs52119391					SNP	G	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:180851093 () rs orientation: forward

Symbol	Name	Function Class
Gm40033	predicted gene, 40033	within coordinates
Srms	src-related kinase lacking C-terminal regulatory tyrosine and N-terminal myristylation sites	within coordinates