rs49069434 SNP Detail

Summary

• ID
  rs49069434
• Variation Type
  SNP
• Alleles
  A/G

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  132
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr1:75555831 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      G CTGCCATGGG TCACAGTAGA CAGACTTAGC TCTGTACCAT
  GTATTGGCTA TGTACTTAGT TCAGCCTGTT TCCATACACC GTGTAATCAC AGCGTGGCTC
  R
  GTTTCAGCCT CAATGCCATC CTGGCTTTTT TAGAGTGTCT AGGAGTAGCT CTGTTCCGCA
  TCCCCATTTA AGCCAGCAGG GCACTGTCAG AAACTGATTC T                    
  
  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	A/J	DBA/2J
ss144696874	ENSMUSSNP828164	ENSEMBL	ENSEMBL_Sanger	f	SNP	A	G
SNP Consensus Information
SNP					Consensus Type	A/J	DBA/2J
rs49069434					SNP	A	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr1:75555831 () rs orientation: forward

Symbol	Name	Function Class
Gm69448	predicted gene, 69448	818 bp upstream