rs47679574 SNP Detail

Summary

• ID
  rs47679574
• Variation Type
  SNP
• Alleles
  C

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  132
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr4:43512269 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      G GGACCTCGTG ATTCTCGGCT ACAACTGAAC TTCCGAGCCA
  CGCAACCCTT GAATGGGCGA ACGATTGAGG CTTCCTTCCC TGCTGCAGAG GATAGCAGCC
  C
  TGAGCCAGGT GCCCAGTTAT CTGATAGCCC ACGTTGACAT ATCCCCAGTC AGGGGTCCTG
  CCTCTTCCTG TGTCTTCATT TGTACCAGCC TGTCCCAGGT A                    
  
  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
ss146240466	ENSMUSSNP1006864	ENSEMBL	ENSEMBL_Sanger	f	SNP	C
SNP Consensus Information
SNP					Consensus Type	A/J
rs47679574					SNP	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:43512269 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Car9	carbonic anhydrase 9			Coding-NonSynonymous
				Intron
				Noncoding-Transcript-Variant
				Noncoding-Transcript-Variant
Rr591017	regulatory region 591017			1213 bp distal