rs45917628 SNP Detail

Summary

• ID
  rs45917628
• Variation Type
  SNP
• Alleles
  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
  Chr7:40835357 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        ACTGTCCTTC AGAAATCTTG ACCTTGCCTT AAGCTCCAGG
  ACTGGAACAA AGAGAGAATG AAAACATGCT TGTGATGAAA GCTGAGCTGT CAATGCCTTG
  G
  GATGCCTATG AGGGCACTTA AAAAAAAAAC AAGACCCATC ACTTCTCCCT TTAGCACACT
  GTGCCATGCT GAAGGTTCTT CACCTCACTG ATACTGGGA                       
  
  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
ss149014247	ENSMUSSNP5955490	ENSEMBL	ENSEMBL_Sanger	f	SNP	G	G
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J
rs45917628					SNP	G	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr7:40835357 () rs orientation: forward

Symbol	Name	Function Class
Gm28667	predicted gene 28667	within coordinates