rs47499637 SNP Detail

Summary

• ID
  rs47499637
• Variation Type
  SNP
• Alleles
  C

• 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
  Chr12:114634404 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              ATATGATCAG CCCAGAGTGG
  TACTATTATA AGGTGTGGTC CTGTTGGAAT AGGTGTCTCA CAAAGTGTGT GGGATATAAA
  ACTCTTAGCT GCTTGGAAGC CATTATTCTG TTAGTATCCT TCAGATGAAA ATGTAGAACA
  CTCATCTTGG CTTGCACTAT GCCTGCATGG ATGCTGTCAT GCTCTCTTGC TTTGATGACA
  C
  AGGATTGAAA TTTTATACTT GTAAATCAGC CCCAATTAAA TGTTTTCCTT CATAATCTTT
  CATCTGTCAT GGTCTCTGTT CACAGCAGTA AAACCCTAAC TATGACATAT GTAAGCCTAT
  TAGGTGTAAA TTCAAGAGCG CAGTATGTTT TCCTGGACAG CACTCTTATT TCTAACCTTT
  AACTCAGAGT TTTCCATTCC                                            
  
  C = C
  

  
  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
ss138795051	ENSMUSSNP2834510	ENSEMBL	ENSEMBL_Sanger	f	SNP	C
SNP Consensus Information
SNP					Consensus Type	A/J
rs47499637					SNP	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr12:114634404 () rs orientation: forward

Symbol	Name	Function Class
Gm46322	predicted gene, 46322	439 bp upstream
Igh	immunoglobulin heavy chain complex	within coordinates
Ighv1-17-1	immunoglobulin heavy variable V1-17-1	1184 bp downstream