cadd.snvs.grch38

is a Product.

CADD v1.7 precomputed raw and PHRED-scaled scores for all possible single nucleotide variants in the GRCh38 human reference genome, tab-separated and bgzip-compressed with a tabix index. A larger version including all annotations is also offered.

URL

whole_genome_SNVs.tsv.gz (81.5 GB)

Format

tsv

License

Warning: No license entered

External IDs

No external IDs available

Latest Version

Unknown

Sources

Original Source(s)

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