rs108463625 SNP Detail

Summary

• ID
  rs108463625
• Variation Type
  SNP
• Alleles
  A/C

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

Genome Location and Flanking Sequence

• Location
  Chr17:7628949 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      C CATAATGTAA GACATTCTCC AGTAAGGAGG TGACCAGTCT
  TTGCTAGGTC ACCCTTCTGG AGTTTTCTTG GCTCCCCTTC TCTACACCAT CACATCCTGC
  M
  GACTCTATAT AGAGAGTGCA CTCCAAACCT GAACACTTCT TACTTTAACC CTCAGGGCAA
  GTGCTGCCCT CATTAATGCC TTCCTAACCT TTCTTCTCCT G                    
  
  M = A/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	A/J
ss145104494	ENSMUSSNP3480172	ENSEMBL	ENSEMBL_Sanger	f	SNP	C	A
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J
rs108463625					SNP	C	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr17:7628949 () rs orientation: forward

Symbol	Name	Function Class
Gm49630	predicted gene, 49630	within coordinates
Gm64723	predicted gene, 64723	within coordinates
Rr336065	regulatory region 336065	within coordinates
Unc93a2	unc-93 homolog A2	1265 bp downstream