ClinVar Miner

Submissions for variant NM_001361.5(DHODH):c.765C>T (p.Ile255=)

gnomAD frequency: 0.00128  dbSNP: rs61757214
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000891618 SCV001035443 likely benign not provided 2023-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV001120251 SCV001278727 likely benign Miller syndrome 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 likely benign is not then subjected to further curation. The score for this variant resulted in a classification of likely benign for this disease.

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