Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
3billion | RCV002283742 | SCV002572783 | uncertain significance | 46,XY sex reversal 3 | 2022-09-01 | criteria provided, single submitter | clinical testing | The variant is not observed in the gnomAD v2.1.1 dataset. In silico tool predictions suggest damaging effect of the variant on gene or gene product (REVEL: 0.99; 3Cnet: 0.85). Same nucleotide change resulting in same amino acid change has been previously reported to be associated with NR5A1-related disorder (PMID: 21691958). Different missense changes at the same codon (p.Cys55Gly, p.Cys55Ser) have been reported to be associated with NR5A1-related disorder (PMID: 31513305 , 32738419). However the evidence of pathogenicity is insufficient at this time. Therefore, this variant is classified as uncertain significance according to the recommendation of ACMG/AMP guideline. |