rs48695063 SNP Detail

Summary

• ID
  rs48695063
• Variation Type
  SNP
• Alleles
  A/C

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr4:143007337 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        CACACCTGTA ACCCCGGTCG GTGCTGGTGG AGGGAAGAGA
  GAGGGTTGCT AGAGCTTACT GGCCAGCCCG TCTAACAGAA CTGGAGTAGT CAGTGAGATA
  M
  CCTGCCTCAA AAATAGATGG AAAGTGACTG AGAAGAAAAT AGACAATATC AGCCTTATAT
  ATGGGCGAGT ATACAGGTCC ACACACCCAC ATATGAAAA                       
  
  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	DBA/2J
ss147778665	ENSMUSSNP2839982	ENSEMBL	ENSEMBL_Sanger	f	SNP	A	C	A
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J
rs48695063					SNP	A	C	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:143007337 () rs orientation: forward

Symbol	Name	Function Class
Pdpn	podoplanin	Intron
Rr604183	regulatory region 604183	1462 bp distal
Rr604184	regulatory region 604184	275 bp distal
Rr604185	regulatory region 604185	365 bp distal
Tssr44446	transcription start site region 44446	1852 bp upstream