CRISPAM

If you use CrisPam, please cite: Roy Rabinowitz, Shiri Almog, Roy Darnell, Daniel Offen. CrisPam: SNP-Derived PAM Analysis Tool for Allele-Specific Targeting of Genetic Variants Using CRISPR-Cas Systems, Front. Genet. 11, 851 (2020), https://doi.org/10.3389/fgene.2020.00851

Optional: Enter rsID

Optional: Enter genomic coordinates

Genome Assembly

Chromosome

Mutation position

Variant Nucleotide

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Optional: Enter a customized PAM here

Alternatively, you may upload multiple SNPs in a CSV file, on this page.

Results

Original Ref. Sequence:

Original Var. Sequence:

The following base editors will correct this variance (and no other bases around it):

Cas	Corrected Sequence	PAM