DaMold

Select genome, assembly & dbSNP
Upload variants VCF/BED file(s)*
Upload variants file(s) : 
Upload Hotspot mutation VCF/BED file
Upload hotspot mutation file : 
Variant selection with genomic effect
 
Entrez gene symbols (e.g. BRCA2, TPTE2)  
 
Use only longest isoform for alternativley spliced genes  
 
RefSeq Transcript IDs (e.g. NM_000059.3, NM_199254.2)  
 
Select only coding region variants  
 
Select variants with amino acid change  
 
Select splice site variants 
  Parameters for variant selection
      

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