Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000556755 | SCV000622216 | pathogenic | Ataxia-telangiectasia syndrome | 2017-02-15 | criteria provided, single submitter | clinical testing | This variant is a gross deletion of the genomic region encompassing exons 2-12, which includes the initiator codon, and part of exon 13 of the ATM gene. The 5' end of this event is located in intron 1 at c.-30-151 and the 3' end is located in exon 13 at c.1922. This deletion is expected to result in an absent or disrupted protein product. While this particular variant has not been reported in the literature, loss-of-function variants in ATM are known to be pathogenic (PMID: 10817650, 19781682). For these reasons, this variant has been classified as Pathogenic. |