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regSNP-splicing

Predict and prioritize disease-causing synonymous single-nucleotide variants that may affect splicing.

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Submit a Variant File or Pasted Input

Upload a Variant Call Format (VCF) file or paste tab-delimited variant lines into the text area below.

Input requirement: The uploaded or pasted data must be in VCF format. A working example is available in the sample input file.
Use this option if you want to submit a file from your computer.
Paste one variant per line using tab-delimited fields.
Select features to display on the result page