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Variant ID | 886 |
---|---|
Genomic Coordinate (GRCh38) | g.22221611del |
Variant | c.1769-2del |
Variant Start Position | 1769 |
Location | Intron 17 |
Amino Acid Change | p.? |
ACMG Call | - |
ACMG Call Last Revised Date | 4/28/2021 |
Predicted ACMG Call | Pathogenic | Effect Type | Splice acceptor |
Variant Type | Splicing |
PMID | 32257293, 34806794 |
Article Count | 2 |
Times Observed | 3-5 |
Clinical Phenotype | - |
ACMG Categories | pvs1, pm2, pp1 |
ACMG Explanations | pvs1: This is a loss of function variant. pm2: chrX:22239727 ref:TAG alt:T was not found in gnomAD exomes or genomes. |
Variant in Clinvar | No |
ClinVar Classification | - |
Categories In Literature | pp1 |
No Contrary Evidence Found | TRUE |
ExAC Allele Frequency | - |
Thousand Genomes Allel Frequency | - |
Ontology Relations | - |
hg19 Mapping Failed | FALSE |
Literature Alleles | X-22239727-TAG-T |
GnomAD Alleles | - |
DBNSFP Alleles | - |
Other Alleles | - |
Note | nan |
Warnings | - |