ClinVar Miner

Submissions for variant NM_004826.4(ECEL1):c.1810G>A (p.Gly604Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
3billion RCV002283883 SCV002573048 uncertain significance Distal arthrogryposis type 5D 2022-09-01 criteria provided, single submitter clinical testing The variant is observed at an extremely low frequency in the gnomAD v2.1.1 dataset (total allele frequency: 0.002%). In silico tool predictions suggest damaging effect of the variant on gene or gene product (REVEL: 0.95; 3Cnet: 0.78). Same nucleotide change resulting in same amino acid change has been previously reported to be associated with ECEL1 -related disorder (PMID: 32566668). 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.

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