rs50456792 SNP Detail

Summary

• ID
  rs50456792
• Variation Type
  SNP
• Alleles
  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
  Chr12:114634094 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      T GTTATAGCTG GGTCATCAGA CAGTAAAATG TCCAGTTTTC
  TAAGAAACTG ATAGAGGACT TTCAACATTG TTAGGATGAC TCTAGACTAT GGGGACTTTG
  G
  AAGTTTGGAG TAAATATACT TTGCATTATG CTTTGCTTAT GTATGACATC CACAAACTCA
  AATGCTTGAA TAAGCCTATG ATAGCCAGGG CGTAAATATG A                    
  
  G = 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	DBA/2J
ss138795036	ENSMUSSNP7235402	ENSEMBL	ENSEMBL_Sanger	f	SNP	G
SNP Consensus Information
SNP					Consensus Type	DBA/2J
rs50456792					SNP	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr12:114634094 () rs orientation: forward

Symbol	Name	Function Class
Gm46322	predicted gene, 46322	749 bp upstream
Igh	immunoglobulin heavy chain complex	within coordinates
Ighv1-17-1	immunoglobulin heavy variable V1-17-1	1494 bp downstream
Rr473858	regulatory region 473858	1889 bp distal