ClinVar Miner

Submissions for variant NM_001079866.2(BCS1L):c.798_799insCACCGGCCTCCACC (p.Asn267fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Myriad Genetics, Inc. RCV002310019 SCV002604269 likely pathogenic Pili torti-deafness syndrome; GRACILE syndrome; Mitochondrial complex III deficiency nuclear type 1 2022-02-25 criteria provided, single submitter clinical testing NM_004328.4(BCS1L):c.798_799ins14(N267Hfs*9) is expected to be pathogenic in the context of BCS1L-related disorders. This variant is predicted to lead to an abnormal or absent protein product due to the creation of a premature termination codon in BCS1L, a gene where loss-of-function variants are known to be pathogenic. Please note: this variant was assessed in the context of healthy population screening.

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