rs108724114 SNP Detail

Summary

• ID
  rs108724114
• Variation Type
  SNP
• Alleles
  G

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

Genome Location and Flanking Sequence

• Location
  Chr9:103232594 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      T CTTCTCCATT TCTTTATCCC TAAGGGAAAA GAAATGTAAT
  CAGTAAATAT TTCTTCTTCA CTAGGGAATT TTGAAAGTAC TCTTCCTCGA ATTTAAAAAG
  G
  AAAAAAAAAA AAAAAAAAAA AAAAAAAGAC CCTAAGGATA ATCCTGGAGA GACAGGAAGA
  GAATACAAAA ATCCTTATCA AACCATTTTA AGGCTTCAAT 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
ss136877195	ENSMUSSNP1672287	ENSEMBL	ENSEMBL_Sanger	f	SNP	G
SNP Consensus Information
SNP					Consensus Type	A/J
rs108724114					SNP	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr9:103232594 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Cdv3	carnitine deficiency-associated gene expressed in ventricle 3			Intron
				mRNA-UTR
D9Mgc22	DNA segment, Chr 9, MRC UK Mouse Genome Centre 22			1910 bp proximal