Public Databases
Databases
alfa
Aggregated allele frequency from dbGaP and dbSNP
alpha-missense
Title of alpha-missense
bayesdel_noaf
BayesDel noAF
cadd_hg19
CADD is a tool for scoring the deleteriousness
cadd_hg38
CADD is a tool for scoring the deleteriousness
cardioboost-arrhythmias-hg19
CardioBoost Arrhythmias
cardioboost-arrhythmias-hg38
CardioBoost Arrhythmias
cardioboost-cardiomyopathies-hg19
CardioBoost Cardiomyopathies
cardioboost-cardiomyopathies-hg38
CardioBoost Cardiomyopathies
ccrs_hg19
Title of ccrs_hg19
ccrs_hg38
Title of ccrs_hg38
clinvar
A Public Database of Genetic Variants
cosmic-genomescreensmutant-hg19
COSMIC v101 GenomeScreensMutant GRCh37
cosmic-genomescreensmutant-hg38
COSMIC v101 GenomeScreensMutant GRCh38
cosmic-noncodingvariants-hg19
COSMIC v101 NonCodingVariants GRCh37
cosmic-noncodingvariants-hg38
COSMIC v101 NonCodingVariants GRCh38
dann_hg19
DANN: Deep Learning-Based Variant Annotation Database
dann_hg38
DANN: Deep Learning-Based Variant Annotation Database, GRCh38 version
dbscsnv-hg19
dbscSNV1.1 hg19
dbscsnv-hg38
dbscSNV1.1 hg38
dbsnp
dbSNP
dbsnp_hg19
The Single Nucleotide Polymorphism Database, hg19
gnomad-exomes-depth
Depth of the GnomAD Exomes
gnomad-exomes2
Genome Aggregation Database Exomes 2.1.1, GRCh37,
gnomad-exomes4
Genome Aggregation Database Exomes 4.1.0, GRCh38,
gnomad-genomes2
Genome Aggregation Database Genomes 2.1.1, GRCh37,
gnomad-genomes4
Genome Aggregation Database Genomes 4.1.0, GRCh38,
gnomad2-exomes-hg19
GnomAD Exomes hg19, v. 2.1.1 - Genome Aggregation Database
gnomad2-genomes-hg19
GnomAD Genomes hg19, v. 2 - Genome Aggregation Database
gnomad3-genomes-depth
Depth of the GnomAD3 Genomes
gnomad3-mito
GnomAD Mitochondrial data
gpn-msa
GPN-MSA - genomic pretrained network with multiple-sequence alignment
helixmtdb
HelixMtDB
mitomap-disease
Mitomap Disease
mitomap-polymorphisms
Mitomap Polymorphisms
mutation-taster
Precomputed MutationTaster 2021 Annotations for Genetic Variant Interpretation
mutsplicedb-hg38
MutSpliceDB HG38
phastcons100_hg19
phastCons100
phastcons100_hg38
phastCons100
phylop100_hg19
phylop100
phylop100_hg38
phylop100
revel
REVEL - Rare Exome Variant Ensemble Learner
revel_hg19
REVEL hg19
spliceai
SOTA Splicing Variants impact predictions
topmed
Topmed
varity
Improved pathogenicity prediction for rare human missense variants