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Variant ID | 848 |
---|---|
Genomic Coordinate (GRCh38) | g.22099021T>A |
Variant | c.949T>A |
Variant Start Position | 949 |
Location | Exon 9 |
Amino Acid Change | p.Tyr317Asn |
ACMG Call | - |
ACMG Call Last Revised Date | 4/28/2021 |
Predicted ACMG Call | Likely Pathogenic | Effect Type | Missense |
Variant Type | SNV |
PMID | 32329911, 34806794 |
Article Count | 2 |
Times Observed | < 3 |
Clinical Phenotype | - |
ACMG Categories | pm2, pm5, pp3, ppc |
ACMG Explanations | pm2: chrX:22117139 ref:T alt:A was not found in gnomAD exomes or genomes. pm5: This is a missense variant at an amino acid residue where a different missense change has been established as pathogenic. 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 | ppc |
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-22117139-T-A |
Other Alleles | X-22117139-TAC-AAT |
Note | nan |
Warnings | - |