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Variant ID | 887 |
---|---|
Genomic Coordinate (GRCh38) | g.22221656_22221657del |
Variant | c.1812del |
Variant Start Position | 1812 |
Location | Exon 18 |
Amino Acid Change | p.Thr605Leufs*14 |
ACMG Call | Pathogenic |
ACMG Call Last Revised Date | 4/28/2021 |
Predicted ACMG Call | - | Effect Type | Frameshift |
Variant Type | Small deletion |
PMID | 34806794 |
Article Count | 1 |
Times Observed | 6-10 |
Clinical Phenotype | Reduced_TmP/GFR_(<LLN), Reduced Serum Phosphate, Gait abnormalities, Lower limb deformities |
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 | - |
Literature Alleles | - |
GnomAD Alleles | - |
DBNSFP Alleles | - |
Other Alleles | - |
Note | nan |
Warnings | - |