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| Variant ID | 354 |
|---|---|
| Genomic Coordinate (GRCh38) | g.22111561G>C |
| Variant | c.1173+1G>C |
| Variant Start Position | 1173 |
| Location | Intron 10 |
| Amino Acid Change | p.? |
| ACMG Call | - |
| ACMG Call Last Revised Date | 4/28/2021 |
| Predicted ACMG Call | Pathogenic | Effect Type | Splice donor |
| Variant Type | Splicing |
| PMID | 25086671 |
| Article Count | 1 |
| Times Observed | < 3 |
| Clinical Phenotype | - |
| ACMG Categories | pvs1, pm2, ppc_het |
| ACMG Explanations | pvs1: This is a loss of function variant. pm2: chrX:22129679 ref:G alt:C was not found in gnomAD exomes or genomes. |
| Variant in Clinvar | Yes |
| ClinVar Classification | Pathogenic |
| Categories In Literature | ppc_het |
| No Contrary Evidence Found | Yes |
| ExAC Allele Frequency | - |
| Thousand Genomes Allel Frequency | - |
| Ontology Relations | - |
| hg19 Mapping Failed | No |
| Literature Alleles | X-22129679-G-C |
| GnomAD Alleles | - |
| DBNSFP Alleles | X-22129679-G-C |
| Other Alleles | - |
| Note | nan |
| Warnings | - |