dbNSFP is an annotation database for non-synonymous SNPs assembled by Xiaoming Liu from the University of Texas School of Public Health (see citation below). With variant tools you can use the dbNSFP database or dbNSFP-light (a version with fewer features) - see which features are offered for each database version below.
There can be frequent changes of name and their meanings of the fields across versions. Please pay close attention to the comments of fields before you use them.
For the latest version dbNSFP 2.4
SIFT_score, lower score means more damaging.SIFT_score_all, SIFT_pred_all, Polyphen2_HDIV_score_all, Polyphen2_HVAR_score_all, Polyphen2_HDIV_pred_all and Polyphen2_HVAR_pred_all. If you need a score for selecting most damaging variants, use fields such as SIFT_score, SIFT_pred, Polyphen2_HDIV_score, Polyphen2_HVAR_score and Polyphen2_HVAR_pred.vtools output might be surprising (e.g. output score 0.4 with criterion ‘score > 0.9’). Use option --all if you would like to see scores for all records.% vtools show annotation dbNSFP -v2
Annotation database dbNSFP (version hg18_hg19_2_1)
Description: dbNSFP version 2.1, maintained by Xiaoming Liu from
UTSPH. Please cite "Liu X, Jian X, and Boerwinkle E. 2011. dbNSFP: a
lightweight database of human non-synonymous SNPs and their functional
predictions. Human Mutation. 32:894-899" and "Liu X, Jian X, and Boerwinkle
E. 2013. dbNSFP v2.0: A Database of Human Nonsynonymous SNVs and Their
Functional Predictions and Annotations. Human Mutation. 34:E2393-E2402." if
you find this database useful.
Database type: variant
Number of records: 89,617,785
Distinct variants: 84,484,850
Reference genome hg18: chr, hg18_pos, ref, alt
Reference genome hg19: chr, pos, ref, alt
Field: chr
Type: string
Comment: Chromosome number
Missing entries: 0
Unique Entries: 24
Field: pos
Type: integer
Comment: physical position on the chromosome as to hg19
(1-based coordinate)
Missing entries: 0
Unique Entries: 28,060,014
Range: 6007 - 249212562
Field: ref
Type: string
Comment: Reference nucleotide allele (as on the + strand)
Missing entries: 0
Unique Entries: 4
Field: alt
Type: string
Comment: Alternative nucleotide allele (as on the + strand)
Missing entries: 0
Unique Entries: 4
Field: aaref
Type: string
Comment: reference amino acid
Missing entries: 0
Unique Entries: 22
Field: aaalt
Type: string
Comment: alternative amino acid
Missing entries: 0
Unique Entries: 22
Field: hg18_pos
Type: integer
Comment: physical position on the chromosome as to hg19
(1-based coordinate)
Missing entries: 44,904 (0.1% of 89,617,785 records)
Unique Entries: 28,043,425
Range: 4381 - 247179185
Field: genename
Type: string
Comment: common gene name
Missing entries: 0
Unique Entries: 20,264
Field: Uniprot_acc
Type: string
Comment: Uniprot accession number. Multiple entries separated
by ";".
Missing entries: 17,068,597 (19.0% of 89,617,785 records)
Unique Entries: 55,816
Field: Uniprot_id
Type: string
Comment: Uniprot ID number. Multiple entries separated by ";".
Missing entries: 20,254,026 (22.6% of 89,617,785 records)
Unique Entries: 37,250
Field: Uniprot_aapos
Type: integer
Comment: amino acid position as to Uniprot. Multiple entries
separated by ";".
Missing entries: 17,068,597 (19.0% of 89,617,785 records)
Unique Entries: 2,687,476
Range: 1 - 9;9;9;9;9;9;9;9;9;9;9;9;9;9;9;9;9;9;9;9;9;9;9;9;9;9;9;9;9
Field: Interpro_domain
Type: string
Comment: Interpro_domain: domain or conserved site on which the
variant locates. Domain annotations come from Interpro
database. The number in the brackets following a
specific domain is the count of times Interpro assigns
the variant position to that domain, typically coming
from different predicting databases. Multiple entries
separated by ";".
Missing entries: 60,454,832 (67.5% of 89,617,785 records)
Unique Entries: 9,922
Field: cds_strand
Type: string
Comment: coding sequence (CDS) strand (+ or -)
Missing entries: 0
Unique Entries: 5
Field: refcodon
Type: string
Comment: reference codon
Missing entries: 2,270,742 (2.5% of 89,617,785 records)
Unique Entries: 1,754
Field: SLR_test_statistic
Type: float
Comment: SLR test statistic for testing natural selection on
codons. A negative value indicates negative selection,
and a positive value indicates positive selection.
Larger magnitude of the value suggests stronger
evidence.
Missing entries: 46,683,780 (52.1% of 89,617,785 records)
Unique Entries: 511,811
Range: -188.177 - 108.85
Field: codonpos
Type: integer
Comment: position on the codon (1, 2 or 3)
Missing entries: 2,270,742 (2.5% of 89,617,785 records)
Unique Entries: 4
Range: 1 - 3;2;3
Field: fold_degenerate
Type: integer
Comment: degenerate type (0, 2 or 3)
Missing entries: 2,270,742 (2.5% of 89,617,785 records)
Unique Entries: 79
Range: 0 - 2;2;2;2;2;2;2;2;2;2;2;2;2;2;2;2;2;2;2;2;2;2;2;2;0
Field: Ancestral_allele
Type: string
Comment: Ancestral allele (based on 1000 genomes reference
data). The following comes from its original README
file: ACTG - high-confidence call, ancestral state
supproted by the other two sequences actg - low-
confindence call, ancestral state supported by one
sequence only N - failure, the ancestral state is
not supported by any other sequence - - the extant
species contains an insertion at this postion . -
no coverage in the alignment
Missing entries: 2,488,820 (2.8% of 89,617,785 records)
Unique Entries: 10
Field: Ensembl_geneid
Type: string
Comment: Ensembl gene id
Missing entries: 0
Unique Entries: 20,839
Field: Ensembl_transcriptid
Type: string
Comment: Ensembl transcript ids (separated by ";")
Missing entries: 0
Unique Entries: 112,159
Field: aapos
Type: integer
Comment: : amino acid position as to the protein "-1" if the
variant is a splicing site SNP (2bp on each end of an
intron)
Missing entries: 0
Unique Entries: 4,315,466
Range: -1 - 9;9;9;9;9;9;9;9;9;9;9;9;9;9;9;9;9;9;9;9;9;9;9;9;9;9;9;9;9;27;9;9;9;9;35;9;9;9
Field: SIFT_score
Type: float
Comment: SIFT score, If a score is smaller than 0.05 the
corresponding NS is predicted as "D(amaging)";
otherwise it is predicted as "T(olerated)".
Missing entries: 12,024,501 (13.4% of 89,617,785 records)
Unique Entries: 101
Range: 0 - 1
Field: SIFT_score_converted
Type: float
Comment: SIFTnew=1-SIFTori. The larger the more damaging.
Missing entries: 12,024,501 (13.4% of 89,617,785 records)
Unique Entries: 101
Range: 0 - 1
Field: SIFT_pred
Type: string
Comment: If SIFTori is smaller than 0.05 (SIFTnew>0.95) the
corresponding NS is predicted as "D(amaging)";
otherwise it is predicted as "T(olerated)".
Missing entries: 12,024,501 (13.4% of 89,617,785 records)
Unique Entries: 2
Field: Polyphen2_HDIV_score_max
Type: float
Comment: The maximum (most damaging) value of Polyphen2 score
based on HumDiv, i.e. hdiv_prob. Use
Polyphen2_HDIV_score to get a list of all scores.
Missing entries: 17,086,068 (19.1% of 89,617,785 records)
Unique Entries: 1,001
Range: 0 - 1
Field: Polyphen2_HDIV_score
Type: string
Comment: Polyphen2 score based on HumDiv, i.e. hdiv_prob. The
score ranges from 0 to 1, and the corresponding
prediction is "probably damaging" if it is in
[0.957,1]; "possibly damaging" if it is in
[0.453,0.956]; "benign" if it is in [0,0.452]. Score
cutoff for binary classification is 0.5, i.e. the
prediction is "neutral" if the score is smaller than
0.5 and "deleterious" if the score is larger than 0.5.
Multiple entries separated by ";".
Missing entries: 17,084,053 (19.1% of 89,617,785 records)
Unique Entries: 8,590,602
Field: Polyphen2_HDIV_pred
Type: string
Comment: Polyphen2 prediction based on HumDiv, "D" ("probably
damaging"), "P" ("possibly damaging") and "B"
("benign"). Multiple entries separated by ";". Because
the availability of multiple values, use expression
such as 'D' in Polyphen2_HDIV_pred instead of 'D' =
Polyphen2_HDIV_pred to filter variants that are
probably damaging.
Missing entries: 17,084,053 (19.1% of 89,617,785 records)
Unique Entries: 83,942
Field: Polyphen2_HVAR_score_max
Type: float
Comment: The maximum (most damaging) value of all Polyphen2
score based on HumVar, i.e. hvar_prob. Use
Polyphen2_HVAR_score_all to get a list of all scores.
Missing entries: 17,086,068 (19.1% of 89,617,785 records)
Unique Entries: 1,001
Range: 0 - 1
Field: Polyphen2_HVAR_score
Type: string
Comment: Polyphen2 score based on HumVar, i.e. hvar_prob. The
score ranges from 0 to 1, and the corresponding
prediction is "probably damaging" if it is in
[0.909,1]; "possibly damaging" if it is in
[0.447,0.908]; "benign" if it is in [0,0.446]. Score
cutoff for binary classification is 0.5, i.e. the
prediction is "neutral" if the score is smaller than
0.5 and "deleterious" if the score is larger than 0.5.
Multiple entries separated by ";".
Missing entries: 17,084,053 (19.1% of 89,617,785 records)
Unique Entries: 10,999,020
Field: Polyphen2_HVAR_pred
Type: string
Comment: Polyphen2 prediction based on HumVar, "D" ("porobably
damaging"), "P" ("possibly damaging") and "B"
("benign"). Multiple entries separated by ";". Because
the availability of multiple values, use expression
such as 'D' in Polyphen2_HVAR_pred instead of 'D' =
Polyphen2_HVAR_pred to filter variants that are
probably damaging.
Missing entries: 17,084,053 (19.1% of 89,617,785 records)
Unique Entries: 83,681
Field: LRT_score
Type: float
Comment: The original LRT two-sided p-value (LRTori).
Missing entries: 21,548,464 (24.0% of 89,617,785 records)
Unique Entries: 826,817
Range: 0 - 1
Field: LRT_score_converted
Type: float
Comment: Converted LRT original p-value (LRTnew). We converted
the LRTori to a score suggested by our Human Muation
(2011) paper: LRTnew=1-LRTori*0.5 if Omega<1, or
LRTnew=LRTori*0.5 if Omega>=1.
Missing entries: 21,548,464 (24.0% of 89,617,785 records)
Unique Entries: 1,168,826
Range: 0 - 1
Field: LRT_pred
Type: string
Comment: LRT prediction, D(eleterious), N(eutral) or U(nknown)
Missing entries: 21,548,464 (24.0% of 89,617,785 records)
Unique Entries: 3
Field: MutationTaster_score
Type: float
Comment: MutationTaster score
Missing entries: 1,143,911 (1.3% of 89,617,785 records)
Unique Entries: 598,533
Range: 0 - 1
Field: MutationTaster_score_converted
Type: float
Comment: The converted score suggested by our Human Mutation
(2011) paper: if the prediction is "A" or "D"
MTnew=MTori; if the prediction is "N" or "P",
MTnew=1-MTori.
Missing entries: 4,373,664 (4.9% of 89,617,785 records)
Unique Entries: 999,050
Range: 0 - 1
Field: MutationTaster_pred
Type: string
Comment: MutationTaster prediction, "A"
("disease_causing_automatic"), "D"
("disease_causing"), "N" ("polymorphism") or "P"
("polymorphism_automatic")
Missing entries: 1,143,911 (1.3% of 89,617,785 records)
Unique Entries: 4
Field: MutationAssessor_score
Type: float
Comment: MutationAssessor functional impact combined score
(MAori)
Missing entries: 14,986,410 (16.7% of 89,617,785 records)
Unique Entries: 2,145
Range: -5.545 - 5.975
Field: MutationAssessor_score_converted
Type: float
Comment: Scaled to 0-1: MAnew=(MAori-(-5.545))/(5.975-(-5.545))
Missing entries: 14,986,410 (16.7% of 89,617,785 records)
Unique Entries: 2,139
Range: 0 - 1
Field: MutationAssessor_pred
Type: string
Comment: MutationAssessor's functional impact of a variant :
predicted functional (high, medium), predicted non-
functional (low, neutral)" Please refer to Reva et al.
Nucl. Acids Res. (2011) 39(17):e118 for details
Missing entries: 14,986,410 (16.7% of 89,617,785 records)
Unique Entries: 4
Field: FATHMM_score
Type: float
Comment: FATHMM default score (weighted for human inherited-
disease mutations with Disease Ontology); If a score
is smaller than -1.5 the corresponding NS is predicted
as "D(AMAGING)"; otherwise it is predicted as
"T(OLERATED)". If there's more than one scores
associated with the same NS due to isoforms, the
smallest score (most damaging) was used. Please refer
to Shihab et al Hum. Mut. (2013) 34(1):57-65 for
details
Missing entries: 19,342,889 (21.6% of 89,617,785 records)
Unique Entries: 2,135
Range: -16.13 - 10.64
Field: FATHMM_score_converted
Type: float
Comment: Scaled to 0-1 and reverse direction (the larger the
more damaging):
FATHMMnew=1-(FATHMMori-(-16.13))/(10.64-(-16.13))
Missing entries: 19,342,889 (21.6% of 89,617,785 records)
Unique Entries: 2,135
Range: 0 - 1
Field: FATHMM_pred
Type: string
Comment: If a FATHMM_score is <=-1.5 the corresponding NS is
predicted as "D(AMAGING)"; otherwise it is predicted
as "T(OLERATED)".
Missing entries: 19,342,889 (21.6% of 89,617,785 records)
Unique Entries: 2
Field: GERP_NR
Type: float
Comment: GERP++ neutral rate
Missing entries: 541,067 (0.6% of 89,617,785 records)
Unique Entries: 1,258
Range: 0.0465 - 6.17
Field: GERP_RS
Type: float
Comment: GERP++ RS score, the larger the score, the more
conserved the site.
Missing entries: 541,067 (0.6% of 89,617,785 records)
Unique Entries: 8,412
Range: -12.3 - 6.17
Field: PhyloP_score
Type: float
Comment: PhyloP score, the larger the score, the more conserved
the site.
Missing entries: 64,695 (0.1% of 89,617,785 records)
Unique Entries: 10,245
Range: -11.958 - 2.941
Field: mg29way_pi
Type: string
Comment: The estimated stationary distribution of A, C, G and T
at the site, using SiPhy algorithm based on 29 mammals
genomes.
Missing entries: 0
Unique Entries: 7,239,991
Field: mg29way_logOdds
Type: float
Comment: SiPhy score based on 29 mammals genomes. The larger
the score, the more conserved the site.
Missing entries: 1,348,155 (1.5% of 89,617,785 records)
Unique Entries: 223,955
Range: 0.0003 - 37.9718
Field: LRT_Omega
Type: float
Comment: estimated nonsynonymous-to-synonymous-rate ratio
(reported by LRT)
Missing entries: 21,548,464 (24.0% of 89,617,785 records)
Unique Entries: 842,708
Range: 0 - 7780.54
Field: UniSNP_ids
Type: string
Comment: "rs numbers from UniSNP, which is a cleaned version of
dbSNP build 129, in format: rs number1;rs number2;..."
Missing entries: 89,510,596 (99.9% of 89,617,785 records)
Unique Entries: 100,701
Field: KGp1_AC
Type: integer
Comment: Alternative allele count in the whole 1000Gp1 data.
Missing entries: 89,278,976 (99.6% of 89,617,785 records)
Unique Entries: 2,172
Range: 0 - 2184
Field: KGp1_AF
Type: float
Comment: Alternative allele frequency in the whole 1000Gp1
data.
Missing entries: 89,278,976 (99.6% of 89,617,785 records)
Unique Entries: 2,571
Range: 0 - 1
Field: KGp1_AFR_AC
Type: integer
Comment: Alternative allele counts in the 1000Gp1 African
descendent samples.
Missing entries: 89,278,976 (99.6% of 89,617,785 records)
Unique Entries: 493
Range: 0 - 492
Field: KGp1_AFR_AF
Type: float
Comment: Alternative allele frequency in the 1000Gp1 African
descendent samples.
Missing entries: 89,278,976 (99.6% of 89,617,785 records)
Unique Entries: 1,062
Range: 0 - 1
Field: KGp1_EUR_AC
Type: integer
Comment: Alternative allele counts in the 1000Gp1 European
descendent samples.
Missing entries: 89,278,976 (99.6% of 89,617,785 records)
Unique Entries: 759
Range: 0 - 758
Field: KGp1_EUR_AF
Type: float
Comment: Alternative allele frequency in the 1000Gp1 European
descendent samples.
Missing entries: 89,278,976 (99.6% of 89,617,785 records)
Unique Entries: 1,185
Range: 0 - 1
Field: KGp1_AMR_AC
Type: integer
Comment: Alternative allele counts in the 1000Gp1 American
descendent samples.
Missing entries: 89,278,976 (99.6% of 89,617,785 records)
Unique Entries: 363
Range: 0 - 362
Field: KGp1_AMR_AF
Type: float
Comment: Alternative allele frequency in the 1000Gp1 American
descendent samples.
Missing entries: 89,278,976 (99.6% of 89,617,785 records)
Unique Entries: 735
Range: 0 - 1
Field: KGp1_ASN_AC
Type: integer
Comment: Alternative allele counts in the 1000Gp1 Asian
descendent samples.
Missing entries: 89,278,976 (99.6% of 89,617,785 records)
Unique Entries: 573
Range: 0 - 572
Field: KGp1_ASN_AF
Type: float
Comment: Alternative allele frequency in the 1000Gp1 Asian
descendent samples.
Missing entries: 89,278,976 (99.6% of 89,617,785 records)
Unique Entries: 939
Range: 0 - 1
Field: ESP6500_AA_AF
Type: float
Comment: Alternative allele frequency in the Afrian American
samples of the NHLBI GO Exome Sequencing Project
(ESP6500 data set).
Missing entries: 88,817,528 (99.1% of 89,617,785 records)
Unique Entries: 27,424
Range: 0 - 1
Field: ESP6500_EA_AF
Type: float
Comment: Alternative allele frequency in the European American
samples of the NHLBI GO Exome Sequencing Project
(ESP6500 data set).
Missing entries: 88,817,528 (99.1% of 89,617,785 records)
Unique Entries: 22,975
Range: 0 - 1
As a quick example, one can use dbNSFP to annotate all of the “damaging” non-synonymous variants from a list of variants. In this example, we find all of the variants predicted to be damaging by SIFT and PolyPhen2 from the master variant table, and we record these variants into a new table called “damaging_ns_snps”.
% vtools select variant "SIFT_pred = 'D' OR PolyPhen2_HDIV_pred like '%D%'" -t damaging_ns_snps
% vtools use dbNSFP_gene --linked_by refGene.name2
% vtools show annotation dbNSFP_gene -v2
Annotation database dbNSFP_gene (version 2_1)
Description: dbNSFP_gene version 2.1, maintained by Dr. Xiaoming
Liu from UTSPH. Please cite "Liu X, Jian X, and Boerwinkle E. 2011. dbNSFP:
a lightweight database of human non-synonymous SNPs and their functional
predictions. Human Mutation. 32:894-899" and "Liu X, Jian X, and Boerwinkle
E. 2013. dbNSFP v2.0: A Database of Human Nonsynonymous SNVs and Their
Functional Predictions and Annotations. Human Mutation. 34:E2393-E2402." if
you find this database useful.
Database type: field
Reference genome *: Gene_name
Gene_name Gene symbol from HGNC
Ensembl_gene Ensembl gene id (from HGNC)
chr Chromosome number (from HGNC)
Gene_old_names Old gene sybmol (from HGNC)
Gene_other_names Other gene names (from HGNC)
Uniprot_acc Uniprot acc number (from HGNC and Uniprot)
Uniprot_id Uniprot id (from HGNC and Uniprot)
Entrez_gene_id Entrez gene id (from HGNC)
CCDS_id CCDS id (from HGNC)
Refseq_id Refseq gene id (from HGNC)
ucsc_id UCSC gene id (from HGNC)
MIM_id MIM gene id (from HGNC)
Gene_full_name Gene full name (from HGNC)
Pathway_Uniprot Pathway(s) the gene belongs to (from Uniprot)
Pathway_ConsensusPathDB Pathway(s) the gene belongs to (from
ConsensusPathDB)
Function_description Function description of the gene (from Uniprot)
Disease_description Disease(s) the gene caused or associated with (from
Uniprot)
MIM_phenotype_id MIM id(s) of the phenotype the gene caused or
associated with (from Uniprot)
MIM_disease MIM disease name(s) with MIM id(s) in "[]" (from
Uniprot)
Trait_association_GWAS Trait(s) the gene associated with (from GWAS catalog)
GO_Slim_biological_process GO Slim terms for biological process
GO_Slim_cellular_component GO Slim terms for cellular component
GO_Slim_molecular_function GO Slim terms for molecular function
Expression_egenetics Tissues/organs the gene expressed in (egenetics data
from BioMart)
Expression_GNF_Atlas Tissues/organs the gene expressed in (GNF/Atlas data
from BioMart)
Interactions_IntAct Other genes the gene interacted with (from IntAct)
gene name followed by Pubmed id in "[]"
Interactions_BioGRID Other genes the gene interacted with (from BioGRID)
gene name followed by Pubmed id in "[]"
Interactions_ConsensusPathDB Other genes the gene interacted with (from
ConsensusPathDB) gene name followed by interaction
confidence in "[]"
P_HI Estimated probability of haploinsufficiency of the
gene from doi:10.1371/journal.pgen.1001154)
P_rec Estimated probability that gene is a recessive disease
gene from doi:10.1126/science.1215040)
Known_rec_info Known recessive status of the gene (from DOI]
10.1126/science.1215040) "lof-tolerant = seen in
homozygous state in at least one 1000G individual"
"recessive = known OMIM recessive disease" original
annotations from DOI:10.1126/science.1215040)
Essential_gene Essential ("E") or Non-essential phenotype-changing
("N") based on Mouse Genome Informatics database. from
doi:10.1371/journal.pgen.1003484
This light version of dbNSFP is only available for dbNSFP 1.0.
vtools show annotation dbNSFP_light -v2
Annotation database dbNSFP_light (version hg18_hg19_1.3)
Description: dbNSFP_light version 1.0, maintained by Xiaoming Liu from UTSPH.
Please cite "Liu X, Jian X, and Boerwinkle E. 2011. dbNSFP: a
lightweight database of human non-synonymous SNPs and their
functional predictions. Human Mutation. 32:894-899" if you find
this database useful.
Database type: variant
Number of records: 73,968,886
Number of distinct variants: 73,754,006
Reference genome hg18: ['chr', 'pos', 'ref', 'alt']
Reference genome hg19: ['chr', 'pos', 'ref', 'alt']
Field: chr
Type: string
Missing entries: 0
Unique Entries: 24
Field: pos
Type: integer
Missing entries: 0
Unique Entries: 24,918,243
Range: 4381 - 247179185
Field: ref
Type: string
Comment: Reference nucleotide allele (as on the + strand)
Missing entries: 0
Unique Entries: 4
Field: alt
Type: string
Comment: Alternative nucleotide allele (as on the + strand)
Missing entries: 0
Unique Entries: 4
Field: aaref
Type: string
Comment: reference amino acid
Missing entries: 0
Unique Entries: 21
Field: aaalt
Type: string
Comment: alternative amino acid
Missing entries: 0
Unique Entries: 21
Field: hg19pos
Type: integer
Comment: physical position on the chromosome as to hg19 (1-based
coordinate)
Missing entries: 33 (0.0% of 73,968,886 records)
Unique Entries: 24,900,697
Range: 15925 - 249212562
Field: PhyloP_score
Type: float
Comment: PhyloP score, phyloPnew=1-0.5x10^phyloPori if phyloPori>0 or
phyloPnew=0.5x10^phyloPori if phyloPori<0
Missing entries: 21,677 (0.0% of 73,968,886 records)
Unique Entries: 6,237
Range: 0 - 0.995645X
Field: SIFT_score
Type: float
Comment: SIFT score, SIFTnew=1-SIFTori
Missing entries: 570,924 (0.8% of 73,968,886 records)
Unique Entries: 167
Range: 0 - 195561991
Field: Polyphen2_score
Type: float
Comment: Polyphen2 score, i.e. pph2_prob
Missing entries: 10,400,231 (14.1% of 73,968,886 records)
Unique Entries: 1,005
Range: 0 - T
Field: LRT_score
Type: float
Comment: LRT score, LRTnew=1-LRTorix0.5 if <1, or LRTnew=LRTorix0.5 if
>=1
Missing entries: 7,795,201 (10.5% of 73,968,886 records)
Unique Entries: 780,594
Range: 0 - T
Field: LRT_pred
Type: string
Comment: LRT prediction, D(eleterious), N(eutral) or U(nknown)
Missing entries: 7,795,201 (10.5% of 73,968,886 records)
Unique Entries: 17
Field: MutationTaster_score
Type: float
Comment: MutationTaster score
Missing entries: 5,514,812 (7.5% of 73,968,886 records)
Unique Entries: 999,920
Range: 0 - W
Field: MutationTaster_pred
Type: string
Comment: MutationTaster prediction, "A" ("disease_causing_automatic"),
"D" ("disease_causing"), "N" ("polymorphism") or "P"
("polymorphism_automatic")
Missing entries: 5,514,843 (7.5% of 73,968,886 records)
Unique Entries: 6
Field: LRT_Omega
Type: float
Comment: estimated nonsynonymous-to-synonymous-rate ratio (reported by
LRT)
Missing entries: 7,795,201 (10.5% of 73,968,886 records)
Unique Entries: 837,566
Range: 0 - 0.995645X
Field: GERP_NR
Type: float
Comment: GERP++ netral rate
Missing entries: 0
Unique Entries: 1,218
Range: 0 - 195561992
Field: GERP_RS
Type: float
Comment: GERP++ RS score
Missing entries: 0
Unique Entries: 8,344
Range: -11.6 - T
Field: uniprot_acc
Type: string
Comment: Uniprot accession number
Missing entries: 0
Unique Entries: 18,766
Field: uniprot_id
Type: string
Comment: Uniprot ID number
Missing entries: 0
Unique Entries: 17,552
Field: uniprot_aapos
Type: integer
Comment: amino acid position as to Uniprot
Missing entries: 0
Unique Entries: 8,815
Range: 0.53741 - Y