Submissions for variant NM_000546.6(TP53):c.884C>A (p.Pro295His)

Total submissions: 1

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp	RCV004701197	SCV005205162	uncertain significance	not specified	2024-06-17	criteria provided, single submitter	clinical testing	Variant summary: TP53 c.884C>A (p.Pro295His) results in a non-conservative amino acid change in the encoded protein sequence. Three of five in-silico tools predict a benign effect of the variant on protein function. The variant was absent in 251492 control chromosomes (gnomAD). The available data on variant occurrences in the general population are insufficient to allow any conclusion about variant significance. To our knowledge, no occurrence of c.884C>A in individuals affected with Li-Fraumeni Syndrome has been reported. The IARC TP53 database reports this variant to be non-functional based on transcriptional activity in yeast (Kato_2003). However, a loss-of-function saturation mutagenesis screen indicated that this missense does not substantially affect TP53 function (Giacomelli_2018). Therefore, these reports do not allow convincing conclusions about the variant effect. The following publications have been ascertained in the context of this evaluation (PMID: 12826609, 30224644). No submitters have cited clinical-significance assessments for this variant to ClinVar. Based on the evidence outlined above, the variant was classified as uncertain significance.