Varaico: Literature-Extracted Genetic Variants

Gene:ROPN1L
Variant:p.P156L
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ROPN1L

NM_031916.5:p.P156L

Associated Papers

Weak A phenotypes associated with novel ABO alleles carrying the A2-related 1061C deletion and various missense substitutions.

Hult AK et al.

Transfusion, 2010

An extensive polymerase chain reaction-allele-specific polymorphism strategy for clinical ABO blood group genotyping that avoids potential errors caused by null, subgroup, and hybrid alleles.

Hosseini-Maaf B et al.

Transfusion, 2007

Genomic analysis of clinical samples with serologic ABO blood grouping discrepancies: identification of 15 novel A and B subgroup alleles.

Olsson ML et al.

Blood, 2001

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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."