ClinVar Miner

Submissions for variant NM_004380.3(CREBBP):c.4150G>A (p.Glu1384Lys)

dbSNP: rs1567272395
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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 RCV002312457 SCV000846964 uncertain significance Inborn genetic diseases 2016-07-13 criteria provided, single submitter clinical testing The p.E1384K variant (also known as c.4150G>A), located in coding exon 25 of the CREBBP gene, results from a G to A substitution at nucleotide position 4150. The glutamic acid at codon 1384 is replaced by lysine, an amino acid with similar properties. 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. In the ESP, this variant was not observed in 6497 samples (12994 alleles) with coverage at this position. This amino acid position is highly conserved in available vertebrate species. In addition, the in silico prediction for this alteration is inconclusive. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

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