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Variant ID | 878 |
---|---|
Genomic Coordinate (GRCh38) | g.22219041T>G |
Variant | c.1706T>G |
Variant Start Position | 1706 |
Location | Exon 17 |
Amino Acid Change | p.Leu569Arg |
ACMG Call | - |
ACMG Call Last Revised Date | 4/28/2021 |
Predicted ACMG Call | Likely Pathogenic | Effect Type | Missense |
Variant Type | SNV |
PMID | 33639975, 34806794 |
Article Count | 2 |
Times Observed | < 3 |
Clinical Phenotype | - |
ACMG Categories | pm2, pp1, pp3 |
ACMG Explanations | pm2: chrX:22237158 ref:T alt:G was not found in gnomAD exomes or genomes. pp3: The SIFT, MutationTaster, and PolyPhen predictions agree that this variant is possibly or probably damaging. |
Variant in Clinvar | No |
ClinVar Classification | - |
Categories In Literature | pp1 |
No Contrary Evidence Found | TRUE |
ExAC Allele Frequency | 0 |
Thousand Genomes Allel Frequency | 0 |
Ontology Relations | - |
hg19 Mapping Failed | FALSE |
Literature Alleles | - |
GnomAD Alleles | - |
DBNSFP Alleles | X-22237158-T-G |
Other Alleles | X-22237157-CTG-AGA X-22237157-CT-AG X-22237158-TG-GC X-22237158-TG-GA X-22237158-TG-GT |
Note | nan |
Warnings | - |