rs49381688 SNP Detail

Summary

• ID
  rs49381688
• 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
  Chr2:125432795 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        CACTCGCTGT CTCACACACT AATTAGTAAG GTATACCTCA
  GACCTCAGGA GAAGGCTACT TTGAGAATAG TTACTCCATA GGATTACCAC ATACTCTGCT
  M
  TGTGCCCCTT TGTACCAGCA CTGCCTCATT CTGTACCTAA TTCAGTAGAT ACCGTTTTAA
  GGTACATGAT GTACGCTGGC CCACTGCTTT CCAGGCAAG                       
  
  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	A/J	MSM/Ms
ss147482178	ENSMUSSNP3032247	ENSEMBL	ENSEMBL_Sanger	f	SNP	C	A
SNP Consensus Information
SNP					Consensus Type	A/J	MSM/Ms
rs49381688					SNP	C	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:125432795 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Cep152	centrosomal protein 152			Intron
				Noncoding-Transcript-Variant
Gm75597	predicted gene, 75597			702 bp upstream
Rr564236	regulatory region 564236			1660 bp proximal
Tssr19898	transcription start site region 19898			766 bp upstream