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| Variant ID | 809 |
|---|---|
| Genomic Coordinate (GRCh38) | g.22247952A>T |
| Variant | c.2249A>T |
| Variant Start Position | 2249 |
| Location | Exon 22 |
| Amino Acid Change | p.*750Leuext*9 |
| ACMG Call | Likely Pathogenic |
| ACMG Call Last Revised Date | 4/28/2021 |
| Predicted ACMG Call | Uncertain Significance | Effect Type | Extension |
| Variant Type | SNV |
| PMID | 21050253, 28383812, 34806794 |
| Article Count | 3 |
| Times Observed | < 3 |
| Clinical Phenotype | - |
| ACMG Categories | pm2, ppc |
| ACMG Explanations | pm2: No extension variants were found in gnomAD exomes or genomes at this position. |
| 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 | - |
| Other Alleles | - |
| Note | nan |
| Warnings | Could not get protein pos and ref for variant id: phex:X750ext. |