rs49078359 SNP Detail

Summary

• ID
  rs49078359
• Variation Type
  SNP
• Alleles
  A/G

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr1:165430836 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        CGGCAGGCAG GACCCAAGGA ATATCTTCCT GCCCACTTTA
  TTAACCGCAA GCGAGAACCA CCGTCTAAAG CATTACTATT GGCCTAGCCT CATGCTGAGA
  R
  CCGTCAATCC CGCTGTATTT AATCACACAC ACTCATGCAA GGGAGCAATA CTCAGCAGAA
  CAGAAGCATT CCAAGCAGTA CCCGAATCAG AGCACGGAG                       
  
  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	A/J	DBA/2J
ss146003129	ENSMUSSNP704618	ENSEMBL	ENSEMBL_Sanger	f	SNP	G	A
SNP Consensus Information
SNP					Consensus Type	A/J	DBA/2J
rs49078359					SNP	G	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr1:165430836 () rs orientation: forward

Symbol	Name	Function Class
Mpzl1	myelin protein zero-like 1	within coordinates
Rr422396	regulatory region 422396	within coordinates
Tssr14771	transcription start site region 14771	1307 bp upstream