rs49362864 SNP Detail

Summary

• ID
  rs49362864
• Variation Type
  SNP
• Alleles
  C

• 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
  Chr3:49449136 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              GTCTCTGTCT CTGTCTCTGT
  CTCTGTCTCT GTCTCTCTCT CTCTGTCTCT CTCTGTCTCT CTGTCTTTTC AGTTCTTGGA
  ACTAAAATTA TATATATATA TATATATTGG ATATTTTCTT TATTTACATT TCATATGTTT
  TCCCCTTTCC AAGTCTCCCC TTCAGAAGCC CCCTATCCCA TCCTCCCTTC CCATGCCTCT
  C
  TGAGGGTGCC CCCCCCCACT CCCATCTTCC CTCCCTGGCA TTCCCCTACA CTGGGGCATC
  GAACATCCTC AGACCCAAGG GCCGCTTCTC CTACTGATGT TCAACAAGGC CATCCTCTGC
  CACATATGTT GCCAGACTCA TAGGTCCATC CATGTGTACT CTTTGGTTGG TGGTACAGTC
  CCCAGGAGCT CCGGTAGGTG                                            
  
  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	A/J
ss135136762	ENSMUSSNP2983972	ENSEMBL	ENSEMBL_Sanger	f	SNP	C
SNP Consensus Information
SNP					Consensus Type	A/J
rs49362864					SNP	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:49449136 () rs orientation: forward

Symbol	Name	Function Class
Rr576096	regulatory region 576096	187 bp proximal