rs46921997 SNP Detail

Summary

• ID
  rs46921997
• Variation Type
  SNP
• Alleles
  T

• 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
  Chr12:114633800 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      T ATCCCATTAT TAGTGAGTGA ACACAATGTG TGCTCTTTTG
  TGACTTGGTT ACCTCACTCA GGATACTTTC AAGTTCCATC CATTTGCCTG TGAAATTCAT
  T
  AAGGCATTTT TTTTAAATAG GGGAATAGTA TTTCATTTTG TAAATATACC ACATTTTCTG
  TATACATTCT TCTGGTGAGG GATAACTGGG TTGTTTTCAG C                    
  
  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	DBA/2J
ss138795009	ENSMUSSNP4121669	ENSEMBL	ENSEMBL_Sanger	f	SNP	T	T
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	DBA/2J
rs46921997					SNP	T	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr12:114633800 () rs orientation: forward

Symbol	Name	Function Class
Gm46322	predicted gene, 46322	1043 bp upstream
Igh	immunoglobulin heavy chain complex	within coordinates
Ighv1-17-1	immunoglobulin heavy variable V1-17-1	1788 bp downstream
Rr473858	regulatory region 473858	1595 bp distal