rs47621426 SNP Detail

Summary

• ID
  rs47621426
• Variation Type
  SNP
• Alleles
  G

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

Genome Location and Flanking Sequence

• Location
  Chr10:38784029 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      C TTGATGCAGG TCCCCAAACA ACTGGAGCAG GGGTTGTCTG
  TGAATTTGTT GTCTGCCTAT GGAACCCGTT CCCTTAACTA GGCTGCCTTG TGCTGCCTCA
  G
  GGGGAGAGAT GTACCTAGTC CTGCAGGGAG GCCATTTTTA AGAACACAGA ATTACAAACT
  GAGTCTGCAA CACAGCCCTT CCTTTCTAGA ACTCGGATAT T                    
  
  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	A/J
ss147062613	ENSMUSSNP1462757	ENSEMBL	ENSEMBL_Sanger	f	SNP	G
SNP Consensus Information
SNP					Consensus Type	A/J
rs47621426					SNP	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr10:38784029 () rs orientation: forward

Symbol	Name	Function Class
Gm66419	predicted gene, 66419	within coordinates
Rr429908	regulatory region 429908	within coordinates