rs50695990 SNP Detail

Summary

• ID
  rs50695990
• Variation Type
  SNP
• Alleles
  A/G

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  138
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr7:34933955 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                        GGATT CCGGGAGGAA AAATCAGCAT
  R
  CTTTGCAGTG CTCAGCGAAG CCAAG                                      
  
  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	129X1/SvJ	DBA/2J
ss148805418	ENSMUSSNP348468	ENSEMBL	ENSEMBL_Sanger	f	SNP	A	G
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	DBA/2J
rs50695990					SNP	A	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr7:34933955 () rs orientation: forward

Symbol	Name	Function Class
Cpgi18864	CpG island 18864	29 bp proximal
Gm38989	predicted gene, 38989	within coordinates
Gm73040	predicted gene, 73040	819 bp upstream
n-TTagt9	nuclear encoded tRNA threonine 9 (anticodon AGT)	240 bp downstream
Rr645337	regulatory region 645337	1145 bp distal
Rr645338	regulatory region 645338	within coordinates
Rr645339	regulatory region 645339	101 bp proximal
Rr645340	regulatory region 645340	163 bp proximal
Rr645341	regulatory region 645341	830 bp proximal