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| Variant ID | 878 |
|---|---|
| Genomic Coordinate (GRCh38) | g.22219041T>G |
| Variant | c.1706T>G |
| Variant Start Position | 1706 |
| Location | Exon 17 |
| Amino Acid Change | p.Leu569Arg |
| ACMG Call | - |
| ACMG Call Last Revised Date | 4/28/2021 |
| Predicted ACMG Call | Likely Pathogenic | Effect Type | Missense |
| Variant Type | SNV |
| PMID | 33639975, 34806794 |
| Article Count | 2 |
| Times Observed | < 3 |
| Clinical Phenotype | - |
| ACMG Categories | pm2, pp1, pp3 |
| ACMG Explanations | pm2: chrX:22237158 ref:T alt:G was not found in gnomAD exomes or genomes. pp3: The SIFT, MutationTaster, and PolyPhen predictions agree that this variant is possibly or probably damaging. |
| Variant in Clinvar | No |
| ClinVar Classification | - |
| Categories In Literature | pp1 |
| No Contrary Evidence Found | TRUE |
| ExAC Allele Frequency | 0 |
| Thousand Genomes Allel Frequency | 0 |
| Ontology Relations | - |
| hg19 Mapping Failed | FALSE |
| Literature Alleles | - |
| GnomAD Alleles | - |
| DBNSFP Alleles | X-22237158-T-G |
| Other Alleles | X-22237157-CTG-AGA X-22237157-CT-AG X-22237158-TG-GC X-22237158-TG-GA X-22237158-TG-GT |
| Note | nan |
| Warnings | - |