ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.66054G>A (p.Glu22018=)

dbSNP: rs727503579
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000152251 SCV000201067 likely benign not specified 2013-04-09 criteria provided, single submitter clinical testing Glu19450Glu in exon 263 of TTN: This variant is not expected to have clinical si gnificance because it does not alter an amino acid residue and is not located wi thin the splice consensus sequence. Glu19450Glu in exon 263 of TTN (allele freq uency = n/a)
Labcorp Genetics (formerly Invitae), Labcorp RCV002056012 SCV002391071 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2024-01-08 criteria provided, single submitter clinical testing
Ambry Genetics RCV002362799 SCV002623891 likely benign Cardiovascular phenotype 2020-10-03 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
Fulgent Genetics, Fulgent Genetics RCV002498712 SCV002794907 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J; Tibial muscular dystrophy; Myopathy, myofibrillar, 9, with early respiratory failure; Early-onset myopathy with fatal cardiomyopathy; Hypertrophic cardiomyopathy 9 2021-08-27 criteria provided, single submitter clinical testing

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