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Variant ID | 857 |
---|---|
Genomic Coordinate (GRCh38) | g.22133557delinsAATAA |
Variant | c.1337delinsAATAA |
Variant Start Position | 1337 |
Location | Exon 12 |
Amino Acid Change | p.Phe446* |
ACMG Call | - |
ACMG Call Last Revised Date | 4/28/2021 |
Predicted ACMG Call | Pathogenic | Effect Type | Nonsense |
Variant Type | Small insertion |
PMID | 29707405, 34806794 |
Article Count | 2 |
Times Observed | < 3 |
Clinical Phenotype | - |
ACMG Categories | pvs1, ps2, ppc |
ACMG Explanations | pvs1: This is a loss of function variant. |
Variant in Clinvar | No |
ClinVar Classification | - |
Categories In Literature | ppc, ps2 |
No Contrary Evidence Found | TRUE |
ExAC Allele Frequency | - |
Thousand Genomes Allel Frequency | - |
Ontology Relations | - |
hg19 Mapping Failed | FALSE |
Literature Alleles | X-22151674-TT-AATAA |
GnomAD Alleles | - |
DBNSFP Alleles | - |
Other Alleles | X-22151674-TT-AA X-22151674-TT-GA X-22151674-TT-AG |
Note | nan |
Warnings | - |