rs49037164 SNP Detail

Summary

• ID
  rs49037164
• Variation Type
  SNP
• Alleles
  G/T

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr2:21797932 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        TATTAAGTTT TTACTCGGCC TTGAGCATTT TATTTGGTAC
  TTTTCAAGGT AACCAAAGCA GAGAGTCATT TCCTCATAAT ATTTTTTTAA AAACTTTTTA
  K
  TGGTTCTTTA TGAATTTCAC ATCGTGTACC CCAATTCTAC TCATCTCATC CCACCCATAC
  ATACATACAT ACTTCCCCCT TGCAGCCTTC CCACAACAG                       
  
  K = G/T
  

  
  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
ss146353874	ENSMUSSNP4774749	ENSEMBL	ENSEMBL_Sanger	f	SNP	G	T
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	DBA/2J
rs49037164					SNP	G	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:21797932 () rs orientation: forward

Symbol	Name	Function Class
Gm24886	predicted gene, 24886	1812 bp downstream
Gm39766	predicted gene, 39766	1980 bp downstream
Gpr158	G protein-coupled receptor 158	within coordinates
Rr41903	regulatory region 41903	1669 bp proximal
Rr372895	regulatory region 372895	within coordinates