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| Variant ID | 786 |
|---|---|
| Genomic Coordinate (GRCh38) | g.22247885C>T |
| Variant | c.2182C>T |
| Variant Start Position | 2182 |
| Location | Exon 22 |
| Amino Acid Change | p.Gln728* |
| ACMG Call | Pathogenic |
| ACMG Call Last Revised Date | 4/28/2021 |
| Predicted ACMG Call | Pathogenic | Effect Type | Nonsense |
| Variant Type | SNV |
| PMID | 31474501, 15057978, 34806794 |
| Article Count | 3 |
| Times Observed | 3-5 |
| Clinical Phenotype | bowed or bent legs, Fractures/Pseudo-Fractures, Gait Abnormalities, Lower Limb Deformities |
| ACMG Categories | pvs1, pm2, ppc |
| ACMG Explanations | pvs1: This is a loss of function variant. pm2: chrX:22266002 ref:C alt:T was not found in gnomAD exomes or genomes. |
| Variant in Clinvar | No |
| ClinVar Classification | - |
| Categories In Literature | ppc |
| No Contrary Evidence Found | Yes |
| ExAC Allele Frequency | - |
| Thousand Genomes Allel Frequency | - |
| Ontology Relations | - |
| hg19 Mapping Failed | No |
| Literature Alleles | - |
| GnomAD Alleles | - |
| DBNSFP Alleles | X-22266002-C-T |
| Other Alleles | X-22266002-CAG-TAA X-22266002-CAG-TGA |
| Note | nan |
| Warnings | - |