rs49741222 SNP Detail

Summary

• ID
  rs49741222
• Variation Type
  SNP
• Alleles
  G

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  132
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr2:35448703 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      C CTGGACCCAG GCGACTCCTA CGGTAGGTGA GCCGCGCCAG
  CTAAGTGGCT AAGTGGCAGA GTTTGGGATT TTAGCCCACT GCTCCAGCAG ACTTTGCTTA
  G
  CTTTGGGAAT CAGAGTTGAA ATGGGTCGGG GGAGGCAGGC ATCTGGGTGC CACCTGGTCT
  CTGGGCTTAG GGCAGACATG GGTGCCCTGG GCCTTGGGTC 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	A/J
ss146415308	ENSMUSSNP162213	ENSEMBL	ENSEMBL_Sanger	f	SNP	G
SNP Consensus Information
SNP					Consensus Type	A/J
rs49741222					SNP	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:35448703 () rs orientation: forward

Symbol	Name	Function Class
Dab2ip	disabled 2 interacting protein	Intron
Gm13446	predicted gene 13446	within coordinates
Rr373036	regulatory region 373036	within coordinates
Rr555707	regulatory region 555707	415 bp distal
Rr555708	regulatory region 555708	within coordinates
Rr555709	regulatory region 555709	1 bp proximal
Tssr17474	transcription start site region 17474	204 bp downstream