rs49366613 SNP Detail

Summary

• ID
  rs49366613
• Variation Type
  SNP
• Alleles
  C

• 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
  Chr12:29192599 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                        TACTT GTGGGAGCCT CAGTTTATCA
  C
  TGCTCCACAA TGTGGGCATT CTGCT                                      
  
  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	129X1/SvJ	A/J	DBA/2J	LG/J	SM/J
ss137517971	ENSMUSSNP5330026	ENSEMBL	ENSEMBL_Sanger	f	SNP	C	C	C
ss323976333	CHEV_12_29827465	CHEVERUD	SCREENING_POP	f	SNP				C	C
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J	LG/J	SM/J
rs49366613					SNP	C	C	C	C	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr12:29192599 () rs orientation: forward

Symbol	Name	Function Class
Gm31333	predicted gene, 31333	within coordinates
Rr464389	regulatory region 464389	661 bp distal
Rr464390	regulatory region 464390	405 bp distal