rs49376997 SNP Detail

Summary

• ID
  rs49376997
• Variation Type
  SNP
• Alleles
  C

• 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
  Chr14:68844655 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        CACTTATGCC AGTCCCTTCC CCATAGTAAA CACCTCAGGT
  GATATGGTTG GGGCTTTTCT CCTTGGTATT AGTGCAGTGG GAAGAAAGAC AATCATAACT
  C
  CATTATAGAT ATCTTATGTG GGTGCAGAAG TGGGCTTACT CTAGAAATAG TAAAGGAAGT
  GCTTTTGTGT TGCTAGGATA AACCAGAAAA TAGGTCTTC                       
  
  C = C
  

  
  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
ss139661475	ENSMUSSNP158792	ENSEMBL	ENSEMBL_Sanger	f	SNP	C	C
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	DBA/2J
rs49376997					SNP	C	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr14:68844655 () rs orientation: forward

Symbol	Name	Function Class
Adam28	a disintegrin and metallopeptidase domain 28	within coordinates
Rr293303	regulatory region 293303	1855 bp distal
Tssr129435	transcription start site region 129435	730 bp upstream