Total submissions: 2
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Illumina Laboratory Services, |
RCV000284956 | SCV000351020 | likely pathogenic | Factor V deficiency | 2017-04-27 | criteria provided, single submitter | clinical testing | The F5 c.2218C>T (p.Arg740Ter) variant, also referred to as c.2308C>T (p.Arg712Ter), is a stop-gained variant that is predicted to result in premature termination of the protein. The p.Arg740Ter variant has been reported in three studies in which it is found in a compound heterozygous state in three individuals with factor V deficiency (Lunghi et al. 1998; Montefusco et al. 2003; Segers et al. 2012). Two of these individuals also carried the factor V Leiden variant and were classified as having pseudo-homozygous activated protein C (APC) resistance; factor V deficiency was also observed in these individuals (Lunghi et al. 1998; Segers et al. 2012). The p.Arg740Ter variant was also detected in one of the probands' son (affected status unknown) and in an unrelated individual who had reduced factor V levels (Lunghi et al. 1998). The variant was also found in two unaffected relatives in a heterozygous state (Montefusco et al. 2003). Control data are unavailable for this variant, which is not found in the 1000 Genomes Project, the Exome Sequencing Project, or the Exome Aggregation Consortium. Based on the evidence and the potential impact of stop-gained variants, the p.Arg740Ter variant is classified as likely pathogenic for Factor V deficiency. This variant was observed by ICSL as part of a predisposition screen in an ostensibly healthy population. |
| Labcorp Genetics |
RCV003595925 | SCV004293803 | pathogenic | Congenital factor V deficiency | 2023-01-20 | criteria provided, single submitter | clinical testing | For these reasons, this variant has been classified as Pathogenic. ClinVar contains an entry for this variant (Variation ID: 293622). This premature translational stop signal has been observed in individual(s) with clinical features of autosomal recessive factor V deficiency (PMID: 9694743, 31399523, 34575869). This variant is not present in population databases (gnomAD no frequency). This sequence change creates a premature translational stop signal (p.Arg740*) in the F5 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in F5 are known to be pathogenic (PMID: 30924984). |