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| Variant ID | 412 |
|---|---|
| Genomic Coordinate (GRCh38) | g.22133552_22133553insAAC |
| Variant | c.1332_1333insAAC |
| Variant Start Position | 1332 |
| Location | Exon 12 |
| Amino Acid Change | p.Trp444_Ala445insAsn |
| ACMG Call | - |
| ACMG Call Last Revised Date | 4/28/2021 |
| Predicted ACMG Call | Likely Pathogenic | Effect Type | Insertion |
| Variant Type | Small insertion |
| PMID | 11004247, 16636593, 34806794 |
| Article Count | 3 |
| Times Observed | < 3 |
| Clinical Phenotype | - |
| ACMG Categories | pm2, pm4, pp1 |
| ACMG Explanations | pm2: chrX:22151669 ref:G alt:GAAC was not found in gnomAD exomes or genomes. pm4: This variant causes an in-frame length change and is not in a repeat region. |
| Variant in Clinvar | No |
| ClinVar Classification | - |
| Categories In Literature | pp1 |
| No Contrary Evidence Found | Yes |
| ExAC Allele Frequency | - |
| Thousand Genomes Allel Frequency | - |
| Ontology Relations | - |
| hg19 Mapping Failed | No |
| Literature Alleles | X-22151669-G-GAAC |
| GnomAD Alleles | - |
| DBNSFP Alleles | - |
| Other Alleles | - |
| Note | nan |
| Warnings | - |