Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000535417 | SCV000643589 | uncertain significance | Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J | 2017-03-25 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV002330893 | SCV002626947 | uncertain significance | Cardiovascular phenotype | 2019-06-07 | criteria provided, single submitter | clinical testing | The p.R14148H variant (also known as c.42443G>A), located in coding exon 152 of the TTN gene, results from a G to A substitution at nucleotide position 42443. The arginine at codon 14148 is replaced by histidine, an amino acid with highly similar properties. 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. |
Revvity Omics, |
RCV003488679 | SCV004237061 | uncertain significance | not provided | 2023-06-30 | criteria provided, single submitter | clinical testing |