rs49191126 SNP Detail

Summary

• ID
  rs49191126
• Variation Type
  SNP
• Alleles
  T

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  142
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr2:119495588 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                        CCCAG CTTGAAATGC TCTTCTTCTT
  T
  TTTTTTTAAT AGTTTAATGT ATTTT                                      
  
  T = 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	A/J	DBA/2J
ss147338613	ENSMUSSNP6012451	ENSEMBL	ENSEMBL_Sanger	f	SNP	T	T	T
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J
rs49191126					SNP	T	T	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:119495588 () rs orientation: forward

Symbol	Name	Function Class
Gm75025	predicted gene, 75025	within coordinates
Gm75032	predicted gene, 75032	within coordinates
H3f3c	H3 histone, family 3C	519 bp downstream
Rr563558	regulatory region 563558	1796 bp distal
Rr563559	regulatory region 563559	825 bp proximal
Tssr25826	transcription start site region 25826	1043 bp downstream