ClinVar Miner

Submissions for variant NM_000546.5(TP53):c.560G>A (p.Gly187Asp) (rs1064795841)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000483175 SCV000572029 uncertain significance not provided 2016-10-13 criteria provided, single submitter clinical testing This variant is denoted TP53 c.560G>A at the cDNA level, p.Gly187Asp (G187D) at the protein level, and results in the change of a Glycine to an Aspartic Acid (GGT>GAT). This variant was observed in multiple lymphoma specimens and in a patient with active chronic lymphocytic leukemia (Kurniawan 2006, Pekova 2011, Munch-Petersen 2016). This variant is reported as having partially functional transactivation in the International Agency for Research on Cancer TP53 database based on functional assays by Kato et al. (2003). TP53 Gly187Asp was not observed in approximately 6,500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, suggesting it is not a common benign variant in these populations. Since Glycine and Aspartic Acid differ in polarity, charge, size or other properties, this is considered a non-conservative amino acid substitution. TP53 Gly187Asp occurs at a position that is not conserved and is located in the DNA binding domain (Bode 2004). In silico analyses are inconsistent regarding the effect this variant may have on protein structure and function. Based on currently available evidence, it is unclear whether TP53 Gly187Asp is a pathogenic or benign variant. We consider it to be a variant of uncertain significance.

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