rs49070231 SNP Detail

Summary

• ID
  rs49070231
• Variation Type
  SNP
• Alleles
  C

• 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
  Chr17:31093635 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                        GGCAC TCCCGAGGTG CAGTTAGATT
  C
  ACTGTGTCCC CTGGGAAACA AGGCC                                      
  
  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
ss145451171	ENSMUSSNP7052285	ENSEMBL	ENSEMBL_Sanger	f	SNP	C	C
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	DBA/2J
rs49070231					SNP	C	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr17:31093635 () rs orientation: forward

Symbol	Name	Function Class
Cpgi8937	CpG island 8937	within coordinates
Dnah8	dynein, axonemal, heavy chain 8	within coordinates
Gm9937	predicted gene 9937	within coordinates
Gm50252	predicted gene, 50252	within coordinates
Rr330583	regulatory region 330583	within coordinates
Rr341200	regulatory region 341200	within coordinates
Tssr147267	transcription start site region 147267	370 bp downstream