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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