rs47816765 SNP Detail

Summary

• ID
  rs47816765
• 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
  Chr2:144075978 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        TTCTAAATAT TTGTCCTTAA ACACACAGAT AGGTGTAGTC
  CTTATCCTTT GTTAAGGAAA CTTCTCTTTG CAACAGACAT AACCATTATA GAAAATCACA
  R
  CCAATAAAAA TGCCGAGTTA TAGCCGGGCG TGGTGGCGCA CGCCTTTAAC CCCAGCACTT
  GGGAGGCAGA GGCAGGCAGA TTTCTGAGTT GGAGGCCAG                       
  
  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	A/J	DBA/2J
ss147788151	ENSMUSSNP1560241	ENSEMBL	ENSEMBL_Sanger	f	SNP	A	G	A
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J
rs47816765					SNP	A	G	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:144075978 () rs orientation: forward

Symbol	Name	Function Class
Gm75267	predicted gene, 75267	within coordinates
Rr397360	regulatory region 397360	208 bp downstream
Rr566413	regulatory region 566413	194 bp distal