rs107726630 SNP Detail

Summary

• ID
  rs107726630
• Variation Type
  SNP
• Alleles
  A/G

• Created in dbSNP Build
  132
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr14:79151303 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        GAAATAATGC TAGCATTTGC TTCATGAATG AGTTGTTGCC
  TAGAAGGTTT GAAGGTTTGG GTTCAAGTCC CTAGTGCACA CTCGTGCATA TATCTCACAG
  R
  GTGGGGCATT ATTCTATACT AAGAAGAAGT CCAGAGCATG GGTGGAAAGA AGTGGTCAGA
  CAGTATGTGA TCTCATTTGT GATAGAAGAA ATGTATCTG                       
  
  R = A/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	129X1/SvJ	DBA/2J
ss139802671	ENSMUSSNP2072537	ENSEMBL	ENSEMBL_Sanger	f	SNP	A	G
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	DBA/2J
rs107726630					SNP	A	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr14:79151303 () rs orientation: forward

Symbol	Name	Function Class
Rr293691	regulatory region 293691	297 bp proximal
Rr293692	regulatory region 293692	697 bp proximal
Rr369884	regulatory region 369884	430 bp upstream
Vwa8	von Willebrand factor A domain containing 8	within coordinates