Varaico: Literature-Extracted Genetic Variants

Gene:MTCH2
Variant:p.F228S
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MTCH2

NM_014342.4:p.F228S

Associated Papers

The Role of RB1 and Secondary Genomic Changes in the Development of Spindle Cell and Pleomorphic Lipomas.

Hellberg M et al.

Genes, Chromosomes & Cancer, 2025

41432308 (PubMed )
Supplement: GCC-64-e70102-s003.xlsx › Summary

Comprehensive genetic analyses of childhood acute leukemia in Iraq using next-generation sequencing.

Al-Kzayer LFY et al.

Translational Pediatrics, 2023

37305720 (PubMed )
Supplement: tp-12-05-827-supplementary.pdf

Exome sequencing of early-onset patients supports genetic heterogeneity in colorectal cancer.

Fernández-Rozadilla C et al.

Scientific Reports, 2021

34045552 (PubMed )
Supplement: 41598_2021_90590_MOESM1_ESM.docx

Novel NOG (p.P42S) mutation causes proximal symphalangism in a four-generation Chinese family.

Sha Y et al.

Bmc Medical Genetics, 2019

31370824 (PubMed )
Supplement: 12881_2019_864_MOESM2_ESM.xlsx › Sheet1

Identification of Targetable Lesions in Anaplastic Thyroid Cancer by Genome Profiling.

Ravi N et al.

Cancers, 2019

30909364 (PubMed )
Supplement: cancers-11-00402-s001.zip › cancers-454918-suppl-final › cancers-454918-Table-S3.xlsx › Sheet1
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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."