Distribution of single‐nucleotide variants on protein–protein interaction sites and its relationship with minor allele frequency-Reference-Cited by-同舟云学术

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Distribution of single‐nucleotide variants on protein–protein interaction sites and its relationship with minor allele frequency

Published:2015-12-09 Issue:2 Volume:25 Page:316-321
ISSN:0961-8368
Container-title:Protein Science
language:en
Short-container-title:Protein Science

Author:

Nishi Hafumi¹,Nakata Junichi²,Kinoshita Kengo¹²³

Affiliation:

1. Department of Applied Information Sciences, Graduate School of Information SciencesTohoku University Miyagi980‐8597 Japan

2. Tohoku Medical Megabank Organization, Tohoku University Miyagi980‐8573 Japan

3. Institute of Development, Aging, and Cancer, Tohoku University Miyagi980‐8575 Japan

Funder

JSPS KAKENHI

Publisher

Wiley

Subject

Molecular Biology,Biochemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pro.2845

Reference22 articles.

1. How to Interpret a Genome-wide Association Study

2. Genomewide Association Studies and Assessment of the Risk of Disease

3. Rare variant association studies: considerations, challenges and opportunities

4. Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes

5. Finding the missing heritability of complex diseases

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1. MTR3D‐AF2: Expanding the coverage of spatially derived missense tolerance scores across the human proteome using AlphaFold2;Protein Science;2024-07-19

2. An Integrated Computational Analysis of High-Risk SNPs in Angiopoietin-like Proteins (ANGPTL3 and ANGPTL8) Reveals Perturbed Protein Dynamics Associated with Cancer;Molecules;2023-06-08

3. An in-silico analysis to identify structural, functional and regulatory role of SNPs in hMRE11;Journal of Biomolecular Structure and Dynamics;2022-01-20

4. Predicting functional consequences of mutations using molecular interaction network features;Human Genetics;2021-08-25

5. Comprehensive characterization of amino acid positions in protein structures reveals molecular effect of missense variants;Proceedings of the National Academy of Sciences;2020-10-26

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