Sponsored by Ultragenyx Pharmaceutical Inc.
Variant ID | 981 |
---|---|
Genomic Coordinate (GRCh38) | g.22247869 |
Variant | - |
Variant Start Position | 2166 |
Location | Exon 22 |
Amino Acid Change | p.Ser722fs |
ACMG Call | - |
ACMG Call Last Revised Date | 4/28/2021 |
Predicted ACMG Call | Pathogenic | Effect Type | Frameshift |
Variant Type | Small insertion |
PMID | 16636593, 34806794 |
Article Count | 2 |
Times Observed | < 3 |
Clinical Phenotype | - |
ACMG Categories | - |
ACMG Explanations | - |
Variant in Clinvar | No |
ClinVar Classification | - |
Categories In Literature | - |
No Contrary Evidence Found | No |
ExAC Allele Frequency | - |
Thousand Genomes Allel Frequency | - |
Ontology Relations | - |
hg19 Mapping Failed | No |
Literature Alleles | - |
GnomAD Alleles | - |
DBNSFP Alleles | - |
Other Alleles | - |
Note | cDNA is not provided |
Warnings | - |