ClinVar Miner

Submissions for variant NM_003982.4(SLC7A7):c.96G>A (p.Lys32=)

gnomAD frequency: 0.00958  dbSNP: rs45479698
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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000186168 SCV000239194 benign not specified 2014-08-14 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Illumina Laboratory Services, Illumina RCV001114967 SCV001272894 benign Lysinuric protein intolerance 2018-01-13 criteria provided, single submitter clinical testing This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score and internal cut-off values, a variant classified as benign is not then subjected to further curation. The score for this variant resulted in a classification of benign for this disease.
Labcorp Genetics (formerly Invitae), Labcorp RCV001114967 SCV001717799 benign Lysinuric protein intolerance 2024-01-31 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001114967 SCV002045753 benign Lysinuric protein intolerance 2021-11-07 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV002262776 SCV002542960 benign Autoinflammatory syndrome 2020-07-01 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004706620 SCV005232754 benign not provided criteria provided, single submitter not provided
Natera, Inc. RCV001114967 SCV001459974 benign Lysinuric protein intolerance 2020-09-16 no assertion criteria provided clinical testing

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