Varaico: Literature-Extracted Genetic Variants

Gene:ACTC1
Variant:p.H42Y
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ACTC1

NM_005159.5:p.H42Y

Associated Papers

Structural and functional analysis of actin point mutations leading to nemaline myopathy to elucidate their role in actin function.

Glyakina AV et al.

Biophysical Reviews, 2022

Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.

Walsh R et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2017

27532257 (PubMed )
Supplement: gim201690x1.zip › Supplementary_Tables_resubmit.xlsx › Table_S1A
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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."