rs49519395 SNP Detail

Summary

• ID
  rs49519395
• Variation Type
  SNP
• Alleles
  A

• 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
  ChrX:111858393 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TCACCTCTCT CTGTGTTCCT
  TCAAGTCCAA TCCCCCAAGT TTATCCTCAG CTCAGTGGCA AACTTCCTGC CTTAGTTAGC
  ATTTCCATTG CTATGAAGAG ATGCCATGAC CAAGGCAACT CTTATAAAGG ACAACATTTT
  AACTGGCGTT GGCTTATAGT TTCAGAGACT CAGTCCATTA TCATCAAGGC AGGAAGCATG
  A
  CAGCATCCAG GCAGATATGG TGCTGAAGAA GGAGCTGAGA GTTCTCCATC TTGATCTGAA
  GTCAGCAAAG AAAAAGAATG ACTCACGAGC AGCTAGGAGG GTCTCAAAGA CCATCCCACA
  GTGACATACT TCCTTCAACA AGGCCACACC TACTCCAACA AGGCCACACC TCCTAATAGT
  GCTACTCCCT GGGCCAAAGA                                            
  
  A = A
  

  
  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
ss134277698	ENSMUSSNP3948861	ENSEMBL	ENSEMBL_Sanger	f	SNP	A	A
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J
rs49519395					SNP	A	A