owencqueen/cgbench_data huggingface dataset:
Gene: GP1BB (HGNC:4440)
Evidence Code: PVS1 — Original ACMG Summary
Null variant (nonsense, frameshift, canonical +/−1 or 2 splice sites, initiation codon, single or multi-exon deletion) in a gene where loss of function (LOF) is a known mechanism of disease.
Caveats:
 • Beware of genes where LOF is not a known disease mechanism (e.g. GFAP, MYH7).
 • Use caution interpreting LOF variants at the extreme 3’ end of a gene.
 • Use caution with splice variants that are predicted to lead to exon skipping but leave the remainder of the protein intact.
 • Use caution in the presence of multiple transcripts.
Gene: GP1BB (HGNC:4440)
Evidence Code: PVS1 — Very Strong
Modification Type: Gene-specific
Use 
GP1BB
 modified decision tree as per SVI WG.
Gene: GP1BB (HGNC:4440)
Evidence Code: PVS1 — Strong
Modification Type: Gene-specific
Use 
GP1BB
 modified decision tree as per SVI WG.
Gene: GP1BB (HGNC:4440)
Evidence Code: PVS1 — Moderate
Modification Type: Gene-specific
Use 
GP1BB
 modified decision tree as per SVI WG.
Gene: GP1BB (HGNC:4440)
Evidence Code: PVS1 — Supporting
Modification Type: Gene-specific
Use 
GP1BB
 modified decision tree as per SVI WG.
Gene: GP1BB (HGNC:4440)
Evidence Code: PS1 — Original ACMG Summary
Same amino acid change as a previously established pathogenic variant regardless of nucleotide change.
Example: Val->Leu caused by either G>C or G>T in the same codon.
Caveat: Beware of changes that impact splicing rather than at the amino acid/protein level.
Gene: GP1BB (HGNC:4440)
Evidence Code: PS1 — Strong
Modification Type: General recommendation
Use as originally specified, but the comparison variant must reach a pathogenic classification using the these rule specifications in order to apply code.
Gene: GP1BB (HGNC:4440)
Evidence Code: PS1 — Moderate
Modification Type: General recommendation
Use as originally specified, but the comparison variant must reach a likely pathogenic classification using the these rule specifications in order to apply code.
Gene: GP1BB (HGNC:4440)
Evidence Code: PS2 — Original ACMG Summary
De novo (both maternity and paternity confirmed) in a patient with the disease and no family history.
Note: Confirmation of paternity only is insufficient. Egg donation, surrogate motherhood, errors in embryo transfer, etc. can contribute to non-maternity.
Gene: GP1BB (HGNC:4440)
Evidence Code: PS2 — Very Strong
Modification Type: Disease-specific
Use proposed SVI point recommendations. See further instruction below. Total of 4 points.
Gene: GP1BB (HGNC:4440)
Evidence Code: PS2 — Strong
Modification Type: Disease-specific
Use proposed SVI point recommendations. See further instruction below. Total of 2 points.
Gene: GP1BB (HGNC:4440)
Evidence Code: PS2 — Moderate
Modification Type: Disease-specific
Use proposed SVI point recommendations. See further instruction below. Total of 1 point.
Gene: GP1BB (HGNC:4440)
Evidence Code: PS3 — Original ACMG Summary
Well-established in vitro or in vivo functional studies supportive of a damaging effect on the gene or gene product.
Note: Functional studies that have been validated and shown to be reproducible and robust in a clinical diagnostic laboratory setting are considered the most well-established.
Gene: GP1BB (HGNC:4440)
Evidence Code: PS3 — Strong
Modification Type: Disease-specific
In a transgenic animal model, must demonstrate minimal to no function.
Gene: GP1BB (HGNC:4440)
Evidence Code: PS3 — Supporting
Modification Type: Disease-specific
Functional assays measuring quantity of GP1ba and/or GPIX expression on cell surface measured by flow cytometry (see spreadsheet for more detail).
Gene: GP1BB (HGNC:4440)
Evidence Code: PS4 — Original ACMG Summary
The prevalence of the variant in affected individuals is significantly increased compared to the prevalence in controls.
Note 1: Relative risk (RR) or odds ratio (OR), as obtained from case-control studies, is >5.0 and the confidence interval around the estimate of RR or OR does not include 1.0. See manuscript for detailed guidance.
Note 2: In instances of very rare variants where case-control studies may not reach statistical significance, the prior observation of the variant in multiple unrelated patients with the same phenotype, and its absence in controls, may be used as moderate level of evidence.
Gene: GP1BB (HGNC:4440)
Evidence Code: PS4 — Moderate
Modification Type: Disease-specific
See instructions below for scoring heterozygous individuals only. Moderate strength applicable for score of 2+ points.
Gene: GP1BB (HGNC:4440)
Evidence Code: PS4 — Supporting
Modification Type: Disease-specific
See instructions below for scoring heterozygous individuals only. Supporting strength applicable for scores ranging from 1-1.75
Gene: GP1BB (HGNC:4440)
Evidence Code: PM1 — Original ACMG Summary
Located in a mutational hot spot and/or critical and well-established functional domain (e.g. active site of an enzyme) without benign variation.
Gene: GP1BB (HGNC:4440)
Evidence Code: PM1 — Moderate
Modification Type: Gene-specific
Disulfide bonds in GPIb are well-established as critical to function, both for interaction with GPIX (PMID: 12036872) and receptor binding to von Willebrand factor (PMID: 18647229). PM1 can be applied when the following cysteine residues (at which there are no known benign variants) are altered: 93, 95, 118, 141, and 147.
Gene: GP1BB (HGNC:4440)
Evidence Code: PM2 — Original ACMG Summary
Absent from controls (or at extremely low frequency if recessive) in Exome Sequencing Project, 1000 Genomes or Exome Aggregation Consortium.
Caveat: Population data for indels may be poorly called by next generation sequencing.
Gene: GP1BB (HGNC:4440)
Evidence Code: PM2 — Supporting
Modification Type: Disease-specific,Gene-specific
gnomAD MAF of less than or equal to 0.00006517.
Gene: GP1BB (HGNC:4440)
Evidence Code: PM3 — Original ACMG Summary
For recessive disorders, detected in trans with a pathogenic variant
Note: This requires testing of parents (or offspring) to determine phase.
Gene: GP1BB (HGNC:4440)
Evidence Code: PM3 — Very Strong
Modification Type: General recommendation
Use proposed SVI point recommendations. Both variants must be classified using these rule specifications, with the exception that a 22q11.2 deletion in trans (
https://www.ncbi.nlm.nih.gov/books/NBK1523/
) may be automatically scored 1pt with confirmation that deletion includes the 
GP1BB
 gene.
Gene: GP1BB (HGNC:4440)
Evidence Code: PM3 — Strong
Modification Type: General recommendation
Use proposed SVI point recommendations. Both variants must be classified using these rule specifications, with the exception that a 22q11.2 deletion in trans (
https://www.ncbi.nlm.nih.gov/books/NBK1523/
) may be automatically scored 1pt with confirmation that deletion includes the 
GP1BB
 gene.
Gene: GP1BB (HGNC:4440)
Evidence Code: PM3 — Moderate
Modification Type: General recommendation
Use proposed SVI point recommendations. Both variants must be classified using these rule specifications, with the exception that a 22q11.2 deletion in trans (
https://www.ncbi.nlm.nih.gov/books/NBK1523/
) may be automatically scored 1pt with confirmation that deletion includes the 
GP1BB
 gene.
Gene: GP1BB (HGNC:4440)
Evidence Code: PM3 — Supporting
Modification Type: General recommendation
Use proposed SVI point recommendations. Both variants must be classified using these rule specifications.
Gene: GP1BB (HGNC:4440)
Evidence Code: PM4 — Original ACMG Summary
Protein length changes due to in-frame deletions/insertions in a non-repeat region or stop-loss variants.
Gene: GP1BB (HGNC:4440)
Evidence Code: PM4 — Moderate
Modification Type: No change
Use with no specification.
Gene: GP1BB (HGNC:4440)
Evidence Code: PM5 — Original ACMG Summary
Novel missense change at an amino acid residue where a different missense change determined to be pathogenic has been seen before.
Example: Arg156His is pathogenic; now you observe Arg156Cys.
Caveat: Beware of changes that impact splicing rather than at the amino acid/protein level.
Gene: GP1BB (HGNC:4440)
Evidence Code: PM5 — Moderate
Modification Type: General recommendation
Use as originally specified, but the comparison variant must reach a pathogenic classification using these rule specifications in order to apply code.
Gene: GP1BB (HGNC:4440)
Evidence Code: PM5 — Supporting
Modification Type: General recommendation
Use as originally specified, but the comparison variant must reach a likely pathogenic classification using these rule specifications in order to apply code.
Gene: GP1BB (HGNC:4440)
Evidence Code: PM6 — Original ACMG Summary
Assumed de novo, but without confirmation of paternity and maternity.
Gene: GP1BB (HGNC:4440)
Evidence Code: PP1 — Original ACMG Summary
Co-segregation with disease in multiple affected family members in a gene definitively known to cause the disease.
Note: May be used as stronger evidence with increasing segregation data.
Gene: GP1BB (HGNC:4440)
Evidence Code: PP1 — Strong
Modification Type: Disease-specific
See instructions below for scoring system. Total segregation score 3+ points.
Gene: GP1BB (HGNC:4440)
Evidence Code: PP1 — Moderate
Modification Type: Disease-specific
See instructions below for scoring system. Total segregation score 2-2.75 points.
Gene: GP1BB (HGNC:4440)
Evidence Code: PP1 — Supporting
Modification Type: Disease-specific
See instructions below for scoring system. Total segregation score 1-1.75 points.
Gene: GP1BB (HGNC:4440)
Evidence Code: PP2 — Original ACMG Summary
Missense variant in a gene that has a low rate of benign missense variation and where missense variants are a common mechanism of disease.
Gene: GP1BB (HGNC:4440)
Evidence Code: PP3 — Original ACMG Summary
Multiple lines of computational evidence support a deleterious effect on the gene or gene product (conservation, evolutionary, splicing impact, etc.).
Caveat: As many in silico algorithms use the same or very similar input for their predictions, each algorithm should not be counted as an independent criterion. PP3 can be used only once in any evaluation of a variant.
Gene: GP1BB (HGNC:4440)
Evidence Code: PP3 — Moderate
Modification Type: Gene-specific
REVEL score of ≥0.773 based on recommendations of Pejaver et al., 2022 (PMID: 36413997).
Gene: GP1BB (HGNC:4440)
Evidence Code: PP3 — Supporting
Modification Type: Gene-specific
REVEL score of ≥0.644 (to <0.773), based on recommendations of Pejaver et al., 2022 (PMID: 36413997).


OR suggested splicing effect using SpliceAI greater than or equal to 0.5.
Gene: GP1BB (HGNC:4440)
Evidence Code: PP4 — Original ACMG Summary
Patient’s phenotype or family history is highly specific for a disease with a single genetic etiology.
Gene: GP1BB (HGNC:4440)
Evidence Code: PP4 — Moderate
Modification Type: Disease-specific
Must meet both criteria:


1)Proband with platelet aggregation study absent for ristocetin and present for all other agonists OR flow cytometry or Western blot less than 10% expression of GPIba 


2)Proband must have full sequencing of all three BSS genes (
GP1BA, GP1BB
 and 
GP9
) and deletion/duplication analysis.
Gene: GP1BB (HGNC:4440)
Evidence Code: PP4 — Supporting
Modification Type: Disease-specific
Proband with platelet aggregation study absent for ristocetin and present for all other agonists, OR 


Flow cytometry or Western blot less than 10% expression of GPIba.
Gene: GP1BB (HGNC:4440)
Evidence Code: PP5 — Original ACMG Summary
Reputable source recently reports variant as pathogenic, but the evidence is not available to the laboratory to perform an independent evaluation.
Gene: GP1BB (HGNC:4440)
Evidence Code: BA1 — Original ACMG Summary
Allele frequency is above 5% in Exome Sequencing Project, 1000 Genomes or Exome Aggregation Consortium.
Gene: GP1BB (HGNC:4440)
Evidence Code: BA1 — Stand Alone
Modification Type: Gene-specific
gnomAD MAF greater than or equal to 0.001 (or 0.1%) in gnomAD.
Gene: GP1BB (HGNC:4440)
Evidence Code: BS1 — Original ACMG Summary
Allele frequency is greater than expected for disorder.
Gene: GP1BB (HGNC:4440)
Evidence Code: BS1 — Strong
Modification Type: Gene-specific
gnomAD MAF greater than or equal to 0.0005 but less than 0.001.
Gene: GP1BB (HGNC:4440)
Evidence Code: BS2 — Original ACMG Summary
Observed in a healthy adult individual for a recessive (homozygous), dominant (heterozygous), or X-linked (hemizygous) disorder, with full penetrance expected at an early age.
Gene: GP1BB (HGNC:4440)
Evidence Code: BS2 — Strong
Modification Type: Disease-specific
Use this rule with 1 or more homozygotes who are unaffected (proven with aggregometry OR flow cytometry AND normal platelet count AND normal platelet size).
Gene: GP1BB (HGNC:4440)
Evidence Code: BS3 — Original ACMG Summary
Well-established in vitro or in vivo functional studies show no damaging effect on protein function or splicing.
Gene: GP1BB (HGNC:4440)
Evidence Code: BS3 — Strong
Modification Type: Disease-specific
Must demonstrate normal aggregometry in a transgenic mouse model
Gene: GP1BB (HGNC:4440)
Evidence Code: BS3 — Supporting
Modification Type: Disease-specific
In a heterologous cell line, must demonstrate BOTH normal expression and normal protein function as compared to wildtype.
Gene: GP1BB (HGNC:4440)
Evidence Code: BS4 — Original ACMG Summary
Lack of segregation in affected members of a family.
Caveat: The presence of phenocopies for common phenotypes (i.e. cancer, epilepsy) can mimic lack of segregation among affected individuals. Also, families may have more than one pathogenic variant contributing to an autosomal dominant disorder, further confounding an apparent lack of segregation.
Gene: GP1BB (HGNC:4440)
Evidence Code: BS4 — Strong
Modification Type: Disease-specific
Variant not tracking in an affected family member.
Gene: GP1BB (HGNC:4440)
Evidence Code: BP1 — Original ACMG Summary
Missense variant in a gene for which primarily truncating variants are known to cause disease.
Gene: GP1BB (HGNC:4440)
Evidence Code: BP2 — Original ACMG Summary
Observed in trans with a pathogenic variant for a fully penetrant dominant gene/disorder or observed in cis with a pathogenic variant in any inheritance pattern.
Gene: GP1BB (HGNC:4440)
Evidence Code: BP2 — Supporting
Modification Type: Disease-specific
Use as written for recessive variants (i.e. - variant must be observed in cis with a pathogenic variant)
Gene: GP1BB (HGNC:4440)
Evidence Code: BP3 — Original ACMG Summary
In frame-deletions/insertions in a repetitive region without a known function.
Gene: GP1BB (HGNC:4440)
Evidence Code: BP3 — Supporting
Modification Type: None
Use with no specification
Gene: GP1BB (HGNC:4440)
Evidence Code: BP4 — Original ACMG Summary
Multiple lines of computational evidence suggest no impact on gene or gene product (conservation, evolutionary, splicing impact, etc)
Caveat: As many in silico algorithms use the same or very similar input for their predictions, each algorithm cannot be counted as an independent criterion. BP4 can be used only once in any evaluation of a variant.
Gene: GP1BB (HGNC:4440)
Evidence Code: BP4 — Supporting
Modification Type: Gene-specific
For a missense variant apply when REVEL score is < 0.290, based on recommendations of Pejaver et al., 2022 (PMID: 36413997) AND SpliceAI score is zero.


OR for a synonymous or intronic variant apply when SpliceAI score is zero.
Gene: GP1BB (HGNC:4440)
Evidence Code: BP5 — Original ACMG Summary
Variant found in a case with an alternate molecular basis for disease.
Gene: GP1BB (HGNC:4440)
Evidence Code: BP6 — Original ACMG Summary
Reputable source recently reports variant as benign, but the evidence is not available to the laboratory to perform an independent evaluation.
Gene: GP1BB (HGNC:4440)
Evidence Code: BP7 — Original ACMG Summary
A synonymous variant for which splicing prediction algorithms predict no impact to the splice consensus sequence nor the creation of a new splice site AND the nucleotide is not highly conserved.
Gene: GP1BB (HGNC:4440)
Evidence Code: BP7 — Supporting
Modification Type: Gene-specific
Use SpliceAI to rule out possible splicing defect (score = 0.2 or less) and reference PhyloP (score = 1.5 or less) to assess conservation.