rs49986214 SNP Detail

Summary

• ID
  rs49986214
• Variation Type
  SNP
• Alleles
  A/G

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  138
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr14:79151398 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                        ATCTC ATTTGTGATA GAAGAAATGT
  R
  TCTGTGCTTT TGTGCACATT GAAGT                                      
  
  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	LG/J	SM/J
ss139802677	ENSMUSSNP7107982	ENSEMBL	ENSEMBL_Sanger	f	SNP	G	A
ss324676547	CHEV_14_79313765	CHEVERUD	SCREENING_POP	f	SNP			A	G
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	DBA/2J	LG/J	SM/J
rs49986214					SNP	G	A	A	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr14:79151398 () rs orientation: forward

Symbol	Name	Function Class
Rr293691	regulatory region 293691	202 bp proximal
Rr293692	regulatory region 293692	602 bp proximal
Rr369884	regulatory region 369884	335 bp upstream
Vwa8	von Willebrand factor A domain containing 8	within coordinates