» Articles » PMID: 33893808

MutationTaster2021

Overview
Specialty Biochemistry
Date 2021 Apr 24
PMID 33893808
Citations 111
Authors
Affiliations
Soon will be listed here.
Abstract

Here we present an update to MutationTaster, our DNA variant effect prediction tool. The new version uses a different prediction model and attains higher accuracy than its predecessor, especially for rare benign variants. In addition, we have integrated many sources of data that only became available after the last release (such as gnomAD and ExAC pLI scores) and changed the splice site prediction model. To more easily assess the relevance of detected known disease mutations to the clinical phenotype of the patient, MutationTaster now provides information on the diseases they cause. Further changes represent a major overhaul of the interfaces to increase user-friendliness whilst many changes under the hood have been designed to accelerate the processing of uploaded VCF files. We also offer an API for the rapid automated query of smaller numbers of variants from within other software. MutationTaster2021 integrates our disease mutation search engine, MutationDistiller, to prioritise variants from VCF files using the patient's clinical phenotype. The novel version is available at https://www.genecascade.org/MutationTaster2021/. This website is free and open to all users and there is no login requirement.

Citing Articles

Identification of mutations associated with congenital cataracts in nineteen Chinese families.

Sun H, Huang T, Liu Z, Xu Y, Wang Y, Wang M BMC Ophthalmol. 2025; 25(1):94.

PMID: 39994538 PMC: 11853334. DOI: 10.1186/s12886-025-03920-4.


A Novel Missense Variant in SORBS2 Is Causative With Familial Alzheimer's Disease.

Wang Q, Wang S, Cao S, Wang Q, Wei Y, Li Y CNS Neurosci Ther. 2025; 31(2):e70256.

PMID: 39912518 PMC: 11800137. DOI: 10.1111/cns.70256.


Deciphering the role of IL17RA in psoriasis and chronic mucocutaneous candidiasis: shared pathways and distinct manifestations.

Kadhi A, Eid E, Massaad M, El-Rassy I, Khoury D, Shimomura Y Front Immunol. 2025; 15:1516408.

PMID: 39911581 PMC: 11796622. DOI: 10.3389/fimmu.2024.1516408.


Somatic DNA Variants in Epilepsy Surgery Brain Samples from Patients with Lesional Epilepsy.

Schwarz J, Becker L, Wahle M, Fassbender J, Thomale U, Tietze A Int J Mol Sci. 2025; 26(2.

PMID: 39859528 PMC: 11766355. DOI: 10.3390/ijms26020815.


Fibronectin Glomerulopathy Without Typical Renal Biopsy Features in a 4-Year-Old Girl with Incidentally Discovered Proteinuria and a G417V Gene Mutation.

Kalmar T, Jakab D, Maroti Z, Pasztor G, Turkevi-Nagy S, Kemeny E Int J Mol Sci. 2025; 26(2.

PMID: 39859354 PMC: 11766185. DOI: 10.3390/ijms26020641.


References
1.
Yeo G, Burge C . Maximum entropy modeling of short sequence motifs with applications to RNA splicing signals. J Comput Biol. 2004; 11(2-3):377-94. DOI: 10.1089/1066527041410418. View

2.
Robinson P, Kohler S, Oellrich A, Wang K, Mungall C, Lewis S . Improved exome prioritization of disease genes through cross-species phenotype comparison. Genome Res. 2013; 24(2):340-8. PMC: 3912424. DOI: 10.1101/gr.160325.113. View

3.
Retterer K, Juusola J, Cho M, Vitazka P, Millan F, Gibellini F . Clinical application of whole-exome sequencing across clinical indications. Genet Med. 2015; 18(7):696-704. DOI: 10.1038/gim.2015.148. View

4.
Lek M, Karczewski K, Minikel E, Samocha K, Banks E, Fennell T . Analysis of protein-coding genetic variation in 60,706 humans. Nature. 2016; 536(7616):285-91. PMC: 5018207. DOI: 10.1038/nature19057. View

5.
Howe K, Achuthan P, Allen J, Allen J, Alvarez-Jarreta J, Amode M . Ensembl 2021. Nucleic Acids Res. 2020; 49(D1):D884-D891. PMC: 7778975. DOI: 10.1093/nar/gkaa942. View