rs47633152 SNP Detail

Summary

• ID
  rs47633152
• Variation Type
  SNP
• Alleles
  C/T

• 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
  Chr1:156840614 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        CAGAGACAAA GCAGATTTTG ATGAAAGAAA AATATGCCTT
  AGTCAGTTGG CAGGATCCTT CTCTGCTCGG CCCACCACAC TGCACTGTTT TGGGGGTGCC
  Y
  GACAGAGGGA CATTTGAGGA GTATGGGTGT TTGTATGTTT GAGTCCAAAG GAGAACGCCA
  GCTCAGAAGT AAATATTTGT CCTGTTGACT ACTAATTCT                       
  
  Y = C/T
  

  
  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
ss145811821	ENSMUSSNP3645804	ENSEMBL	ENSEMBL_Sanger	f	SNP	T	C
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	DBA/2J
rs47633152					SNP	T	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr1:156840614 () rs orientation: forward

Symbol	Name	Function Class
Gm28694	predicted gene 28694	within coordinates
Gm70243	predicted gene, 70243	within coordinates
Rr421310	regulatory region 421310	within coordinates