ClinVar Miner

Submissions for variant NM_198994.3(TGM6):c.1103G>A (p.Arg368Gln)

gnomAD frequency: 0.00731  dbSNP: rs75122556
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000312139 SCV000433151 benign Spinocerebellar ataxia type 35 2018-01-12 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.
Invitae RCV000881675 SCV001024865 benign not provided 2024-01-23 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV001288873 SCV001476270 benign not specified 2019-12-27 criteria provided, single submitter clinical testing
GeneDx RCV000881675 SCV002522049 likely benign not provided 2021-05-05 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.

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