rs108535431 SNP Detail

Summary

• ID
  rs108535431
• Variation Type
  SNP
• Alleles
  C

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

Genome Location and Flanking Sequence

• Location
  Chr3:77899711 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      T GATTTGCATT TCCCTGATGA CTAAGGATGT TGAACATTTC
  TTTAGGTGCT TCTCAGCAAT TCGGTATTCC TCAGCTGAGA ATTCTTTGTT TTGCTCTGTA
  C
  CCCATTTTTA ATAGGGTTAT TTCGTTCTCT GAAGTCTACC TTCTTGAGTT CTTTGTTATA
  TATTGGATAT TAGCCCTCTA TCAGATGTAA GGTTGGTAAA 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	A/J
ss137792692	ENSMUSSNP6208572	ENSEMBL	ENSEMBL_Sanger	f	SNP	C
SNP Consensus Information
SNP					Consensus Type	A/J
rs108535431					SNP	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:77899711 () rs orientation: forward

Symbol	Name	Function Class
Gm64396	predicted gene, 64396	within coordinates
Rr578410	regulatory region 578410	1190 bp proximal