Varaico: Literature-Extracted Genetic Variants

Gene:CFAP298
Variant:p.V132_C133insFs
Back to variants list

CFAP298

NM_021254.4:p.V132_C133insFs

Associated Papers

Whole-exome sequencing reveals a monogenic cause in 56% of individuals with laterality disorders and associated congenital heart defects.

Bolkier Y et al.

Journal of Medical Genetics, 2022

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

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."