ClinVar Miner

Submissions for variant NM_013382.5(POMT2):c.162G>T (p.Ala54=) (rs2270420)

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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000081566 SCV000113497 benign not specified 2012-10-25 criteria provided, single submitter clinical testing
Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine RCV000081566 SCV000269715 benign not specified 2015-01-13 criteria provided, single submitter clinical testing p.Ala54Ala in exon 1 of POMT2: This variant is not expected to have clinical sig nificance because it does not alter an amino acid residue and is not located wit hin the splice consensus sequence. It has been identified in 5.8% (478/8280) of European American chromosomes from a broad population by the NHLBI Exome Sequenc ing Project (http://evs.gs.washington.edu/EVS; dbSNP rs2270420).
PreventionGenetics,PreventionGenetics RCV000081566 SCV000311984 benign not specified criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000365540 SCV000388989 likely benign Limb-Girdle Muscular Dystrophy, Recessive 2016-06-14 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000081566 SCV000614753 benign not specified 2017-07-26 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000081566 SCV000152366 likely benign not specified no assertion criteria provided clinical testing Likely benign based on allele frequency in 1000 Genomes Project or ESP global frequency and its presence in a patient with a rare or unrelated disease phenotype. NOT Sanger confirmed.

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