MutPred Splice Logo
Identifying coding region variants which disrupt pre-mRNA splicing and the underlying mechanism (v1.3.2)
Note: Click the submit button or refresh the page to clear the form
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
OR ALTERNATIVELY
2b, Upload a VCF (Variant Call Format) file:

3, Send data for analysis:
 
 
 
 
Note: Service currently running at risk, smaller jobs have priority!
If you need to run a large dataset then please contact us