Total submissions: 2
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Broad Center for Mendelian Genomics, |
RCV000001471 | SCV003922189 | likely pathogenic | Iron-refractory iron deficiency anemia | 2023-05-02 | criteria provided, single submitter | curation | The heterozygous p.Glu452GlyfsTer6 variant in TMPRSS6 was identified by our study, in the compound heterozygous state with a likely pathogenic variant (ClinVar Variation ID: 1405), in one individual with iron-refractory iron deficiency anemia. This individual also carried a likely pathogenic variant (ClinVar Variation ID: 1405), however the phase of these variants is unknown at this time. The p.Glu452GlyfsTer6 variant in TMPRSS6 has been previously reported in one individual with iron-refractory iron deficiency anemia (PMID: 18408718) but has been identified in 0.005% (2/41478) of African/African American chromosomes by the Genome Aggregation Database (gnomAD, http://gnomad.broadinstitute.org; dbSNP ID: rs1384933966). Although this variant has been seen in the general population in a heterozygous state, its frequency is low enough to be consistent with a recessive carrier frequency. This previously reported individual (PMID: 18408718) was a compound heterozygote that carried a reported likely pathogenic variant in unknown phase (ClinVar Variation ID: 1405), which increases the likelihood that the p.Glu452GlyfsTer6 variant is pathogenic. This variant has also been reported in ClinVar (Variation ID: 1406) and has been interpreted as pathogenic by OMIM. This variant is predicted to cause a frameshift, which alters the protein’s amino acid sequence beginning at position 452 and leads to a premature termination codon 6 amino acids downstream. This alteration is then predicted to lead to a truncated or absent protein. Loss of function of the TMPRSS6 gene is an established disease mechanism in autosomal recessive iron-refractory iron deficiency anemia. In summary, although additional studies are required to fully establish its clinical significance, this variant is likely pathogenic for autosomal recessive iron-refractory iron deficiency anemia. ACMG/AMP Criteria applied: PVS1, PM2_Supporting (Richards 2015). |
| OMIM | RCV000001471 | SCV000021626 | pathogenic | Iron-refractory iron deficiency anemia | 2008-05-01 | no assertion criteria provided | literature only |