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| Variant ID | 857 |
|---|---|
| Genomic Coordinate (GRCh38) | g.22133557delinsAATAA |
| Variant | c.1337delinsAATAA |
| Variant Start Position | 1337 |
| Location | Exon 12 |
| Amino Acid Change | p.Phe446* |
| ACMG Call | - |
| ACMG Call Last Revised Date | 4/28/2021 |
| Predicted ACMG Call | Pathogenic | Effect Type | Nonsense |
| Variant Type | Small insertion |
| PMID | 29707405, 34806794 |
| Article Count | 2 |
| Times Observed | < 3 |
| Clinical Phenotype | - |
| ACMG Categories | pvs1, ps2, ppc |
| ACMG Explanations | pvs1: This is a loss of function variant. |
| Variant in Clinvar | No |
| ClinVar Classification | - |
| Categories In Literature | ppc, ps2 |
| No Contrary Evidence Found | TRUE |
| ExAC Allele Frequency | - |
| Thousand Genomes Allel Frequency | - |
| Ontology Relations | - |
| hg19 Mapping Failed | FALSE |
| Literature Alleles | X-22151674-TT-AATAA |
| GnomAD Alleles | - |
| DBNSFP Alleles | - |
| Other Alleles | X-22151674-TT-AA X-22151674-TT-GA X-22151674-TT-AG |
| Note | nan |
| Warnings | - |