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Identifying coding region variants which disrupt pre-mRNA splicing and the underlying mechanism (v1.3.2)
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1, Enter your email address
2a, Enter genomic coordinates (hg19), strand and substitution (one per line) for exonic variants in the following comma delimited format:
chromosome, coordinate, strand (+ or -), refBase, altBase
Click here for some example data     Click here to download an example of a VCF file     Click here to view a sample of results
2b, Upload a VCF (Variant Call Format) file:

3, Send data for analysis:
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If you need to run a large dataset then please contact us