rs47481130 SNP Detail

Summary

• ID
  rs47481130
• 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
  

Genome Location and Flanking Sequence

• Location
  Chr17:31058663 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      T GAAGTTGTTG CCTCAAACCA GCCTAGGCAT TCAACGACTT
  TCTCCCACCT CTTCAAAAGA AGTCTGTATA TTTGTTCTCT CCCCGTTTTG TTACAGATAG
  C
  GTTGTTTTGT TACAGATAAT CAATTCATAT GGGCAAAAAG TGTCTTCAGG CTAACAGCAA
  TGGAGGTTGG GCAGCAAATA CATTTGCTTC CTGTGGCTAG G                    
  
  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	DBA/2J
ss145450285	ENSMUSSNP5162302	ENSEMBL	ENSEMBL_Sanger	f	SNP	C
SNP Consensus Information
SNP					Consensus Type	DBA/2J
rs47481130					SNP	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr17:31058663 () rs orientation: forward

Symbol	Name	Function Class
Dnah8	dynein, axonemal, heavy chain 8	within coordinates
Gm50252	predicted gene, 50252	within coordinates
Rr330577	regulatory region 330577	1538 bp proximal
Rr334763	regulatory region 334763	within coordinates