rs31244366 SNP Detail

Summary

• ID
  rs31244366
• Variation Type
  SNP
• Alleles
  A/G

• Created in dbSNP Build
  125
• Last Updated in dbSNP Build
  138
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr3:10157318 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                        GTGTG TTTCTAGATT AACAGAGATA
  R
  CAAGACTCAC TCTAACTGTG GACAA                                      
  
  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	129S1/SvImJ	129X1/SvJ	A/J	C57BL/6J	DBA/2J	LG/J	SM/J
ss45513946	mCV25352588	ABI	CRAMUS_MOUSE	f	SNP	A	A	A	G	G
ss134580076	ENSMUSSNP5145148	ENSEMBL	ENSEMBL_Sanger	f	SNP		A	A		G
ss320652925	CHEV_3_10092258	CHEVERUD	SCREENING_POP	f	SNP						A	G
SNP Consensus Information
SNP					Consensus Type	129S1/SvImJ	129X1/SvJ	A/J	C57BL/6J	DBA/2J	LG/J	SM/J
rs31244366					SNP	A	A	A	G	G	A	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:10157318 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Myef2l	myelin expression factor 2 like			Coding-NonSynonymous
				Noncoding-Transcript-Variant
Rr573569	regulatory region 573569			282 bp proximal