Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Neuberg Centre For Genomic Medicine, |
RCV003388735 | SCV004100484 | likely pathogenic | Epidermolysis bullosa simplex 1A, generalized severe | criteria provided, single submitter | clinical testing | The frameshift deletion p.E205Gfs*4 in KRT14 (NM_000526.5) has not been reported previously as a pathogenic variant nor as a benign variant, to our knowledge. The p.E205Gfs*4 variant is novel (not in any individuals) in gnomAD Exomes and is novel (not in any individuals) in 1000 Genomes. This variant is predicted to cause loss of normal protein function through protein truncation. For these reasons, this variant has been classified as Likely Pathogenic. |