ClinVar Miner

Submissions for variant NM_001395413.1(POR):c.678C>T (p.Ala226=)

gnomAD frequency: 0.00089  dbSNP: rs72557906
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000732197 SCV000860117 uncertain significance not provided 2018-03-22 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000732197 SCV000884406 likely benign not provided 2020-04-02 criteria provided, single submitter clinical testing
Invitae RCV001087288 SCV001098193 likely benign Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency 2024-02-01 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV001087288 SCV001320889 uncertain significance Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency 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, this variant could not be ruled out of causing disease and therefore its association with disease required further investigation. A literature search was performed for the gene, cDNA change, and amino acid change (if applicable). No publications were found based on this search. This variant was therefore classified as a variant of unknown significance for this disease.
GeneDx RCV000732197 SCV001792586 likely benign not provided 2019-09-09 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000732197 SCV001962051 likely benign not provided 2023-11-01 criteria provided, single submitter clinical testing POR: BP4, BP7

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