Varaico: Literature-Extracted Genetic Variants

Gene:EPHA2
Variant:p.V949L
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EPHA2

NM_004431.5:p.V949L

Associated Papers

Detection Rate of Cataract-Related Gene Variants in Sporadic Childhood Cataract Patients in Southern China.

Luo Z et al.

American Journal of Ophthalmology, 2025

Homologous recombination deficiency in diverse cancer types and its correlation with platinum chemotherapy efficiency in ovarian cancer.

Wen H et al.

Bmc Cancer, 2022

35578198 (PubMed )
Supplement: 12885_2022_9602_MOESM9_ESM.xlsx › Table_S6

Feeding difficulty is the dominant feature in 12 Chinese newborns with CHD7 pathogenic variants.

Chen X et al.

Bmc Medical Genetics, 2019

31146700 (PubMed )
Supplement: 12881_2019_813_MOESM1_ESM.xls › CHD7_ChenXiang_query_Report_Fil
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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."