ClinVar Miner

Submissions for variant NM_201384.3(PLEC):c.5863G>A (p.Ala1955Thr)

gnomAD frequency: 0.00003  dbSNP: rs200374705
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000733709 SCV000861802 uncertain significance not provided 2018-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000816286 SCV000956787 uncertain significance Epidermolysis bullosa simplex 5B, with muscular dystrophy; Epidermolysis bullosa simplex, Ogna type; Epidermolysis bullosa simplex 5C, with pyloric atresia; Autosomal recessive limb-girdle muscular dystrophy type 2Q; Epidermolysis bullosa simplex with nail dystrophy 2024-02-24 criteria provided, single submitter clinical testing This sequence change replaces alanine, which is neutral and non-polar, with threonine, which is neutral and polar, at codon 1982 of the PLEC protein (p.Ala1982Thr). This variant is present in population databases (rs200374705, gnomAD 0.1%). This variant has not been reported in the literature in individuals affected with PLEC-related conditions. ClinVar contains an entry for this variant (Variation ID: 597551). Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.
Ambry Genetics RCV002535348 SCV003690001 uncertain significance Inborn genetic diseases 2021-08-12 criteria provided, single submitter clinical testing The c.5944G>A (p.A1982T) alteration is located in exon 32 (coding exon 31) of the PLEC gene. This alteration results from a G to A substitution at nucleotide position 5944, causing the alanine (A) at amino acid position 1982 to be replaced by a threonine (T). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.
Revvity Omics, Revvity RCV000733709 SCV003809111 uncertain significance not provided 2019-06-12 criteria provided, single submitter clinical testing

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