ClinVar Miner

Submissions for variant NM_000975.5(RPL11):c.396+3A>G

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV002357679 SCV002622978 uncertain significance Diamond-Blackfan anemia 2015-01-19 criteria provided, single submitter clinical testing The c.396+3A>G intronic variant results from an A to G substitution 3 nucleotides after coding exon 4 in the RPL11 gene. This variant was previously reported in the SNPDatabase as rs113058387. This variant was not reported in population-based cohorts in the following databases: Database of Single Nucleotide Polymorphisms (dbSNP), NHLBI Exome Sequencing Project (ESP) and 1000 Genomes Project. This nucleotide position is highly conserved in available vertebrate species. Using the BDGP splice site prediction tool, this alteration is predicted to signficantly weaken the native splice donor site efficiency. Using the ESEfinder splice site prediction tool, this alteration is predicted to only slightly weaken the native splice donor site efficiency. However, direct evidence is unavailable. Since supporting evidence is limited at this time, the clinical significance of this variant remains unclear.

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