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GeneBe API Showcase
This page demonstrates how to use the GeneBe API to query variant information. The API provides programmatic access to genomic annotations and variant data.
API presented here should be used for checking single variants. If you want to check many variants at once, please use other API endpoints that you will find in the documentation.
Documentation & Advanced Usage
• Complete API documentation:docs.genebe.net/docs/api/overview/
• Interactive endpoint tester:api.genebe.net/cloud/gb-api-doc/swagger-ui/
• Python client for pandas:pypi.org/project/genebe/
• Java CLI for VCF files:github.com/pstawinski/genebe-cli
• All tools documented at:docs.genebe.net
API Request Examples for Variant: 6-75886094-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=6&pos=75886094&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 0,
"criteria": [
"PP3_Strong"
],
"effects": [
"missense_variant",
"splice_region_variant"
],
"gene_symbol": "MYO6",
"hgnc_id": 7605,
"hgvs_c": "c.2507G>A",
"hgvs_p": "p.Arg836His",
"inheritance_mode": "AD,AR",
"pathogenic_score": 4,
"score": 4,
"transcript": "NM_001368865.1",
"verdict": "Uncertain_significance"
}
],
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PP3_Strong",
"acmg_score": 4,
"allele_count_reference_population": 6,
"alphamissense_prediction": null,
"alphamissense_score": 0.4416,
"alt": "A",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Pathogenic",
"bayesdelnoaf_score": 0.25,
"chr": "6",
"clinvar_classification": "Uncertain significance",
"clinvar_disease": "not specified",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"computational_prediction_selected": "Uncertain_significance",
"computational_score_selected": 0.6848322153091431,
"computational_source_selected": "MetaRNN",
"consequences": [
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1285,
"aa_ref": "R",
"aa_start": 836,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8615,
"cdna_start": 2739,
"cds_end": null,
"cds_length": 3858,
"cds_start": 2507,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_count": 35,
"exon_rank": 24,
"exon_rank_end": null,
"feature": "NM_004999.4",
"gene_hgnc_id": 7605,
"gene_symbol": "MYO6",
"hgvs_c": "c.2507G>A",
"hgvs_p": "p.Arg836His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000369977.8",
"protein_coding": true,
"protein_id": "NP_004990.3",
"strand": true,
"transcript": "NM_004999.4",
"transcript_support_level": null
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1285,
"aa_ref": "R",
"aa_start": 836,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 8615,
"cdna_start": 2739,
"cds_end": null,
"cds_length": 3858,
"cds_start": 2507,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_count": 35,
"exon_rank": 24,
"exon_rank_end": null,
"feature": "ENST00000369977.8",
"gene_hgnc_id": 7605,
"gene_symbol": "MYO6",
"hgvs_c": "c.2507G>A",
"hgvs_p": "p.Arg836His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_004999.4",
"protein_coding": true,
"protein_id": "ENSP00000358994.3",
"strand": true,
"transcript": "ENST00000369977.8",
"transcript_support_level": 1
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1262,
"aa_ref": "R",
"aa_start": 836,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4026,
"cdna_start": 2539,
"cds_end": null,
"cds_length": 3789,
"cds_start": 2507,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_count": 32,
"exon_rank": 23,
"exon_rank_end": null,
"feature": "ENST00000615563.4",
"gene_hgnc_id": 7605,
"gene_symbol": "MYO6",
"hgvs_c": "c.2507G>A",
"hgvs_p": "p.Arg836His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000478013.1",
"strand": true,
"transcript": "ENST00000615563.4",
"transcript_support_level": 1
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1294,
"aa_ref": "R",
"aa_start": 836,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8642,
"cdna_start": 2739,
"cds_end": null,
"cds_length": 3885,
"cds_start": 2507,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_count": 36,
"exon_rank": 24,
"exon_rank_end": null,
"feature": "NM_001368865.1",
"gene_hgnc_id": 7605,
"gene_symbol": "MYO6",
"hgvs_c": "c.2507G>A",
"hgvs_p": "p.Arg836His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001355794.1",
"strand": true,
"transcript": "NM_001368865.1",
"transcript_support_level": null
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1294,
"aa_ref": "R",
"aa_start": 836,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8642,
"cdna_start": 2739,
"cds_end": null,
"cds_length": 3885,
"cds_start": 2507,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_count": 36,
"exon_rank": 24,
"exon_rank_end": null,
"feature": "ENST00000664640.1",
"gene_hgnc_id": 7605,
"gene_symbol": "MYO6",
"hgvs_c": "c.2507G>A",
"hgvs_p": "p.Arg836His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000499278.1",
"strand": true,
"transcript": "ENST00000664640.1",
"transcript_support_level": null
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1285,
"aa_ref": "R",
"aa_start": 836,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8615,
"cdna_start": 2739,
"cds_end": null,
"cds_length": 3858,
"cds_start": 2507,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_count": 35,
"exon_rank": 24,
"exon_rank_end": null,
"feature": "NM_001368866.1",
"gene_hgnc_id": 7605,
"gene_symbol": "MYO6",
"hgvs_c": "c.2507G>A",
"hgvs_p": "p.Arg836His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001355795.1",
"strand": true,
"transcript": "NM_001368866.1",
"transcript_support_level": null
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1285,
"aa_ref": "R",
"aa_start": 836,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3858,
"cdna_start": 2507,
"cds_end": null,
"cds_length": 3858,
"cds_start": 2507,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_count": 34,
"exon_rank": 23,
"exon_rank_end": null,
"feature": "ENST00000672093.1",
"gene_hgnc_id": 7605,
"gene_symbol": "MYO6",
"hgvs_c": "c.2507G>A",
"hgvs_p": "p.Arg836His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000500710.1",
"strand": true,
"transcript": "ENST00000672093.1",
"transcript_support_level": null
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1285,
"aa_ref": "R",
"aa_start": 836,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5303,
"cdna_start": 2786,
"cds_end": null,
"cds_length": 3858,
"cds_start": 2507,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_count": 36,
"exon_rank": 25,
"exon_rank_end": null,
"feature": "ENST00000947981.1",
"gene_hgnc_id": 7605,
"gene_symbol": "MYO6",
"hgvs_c": "c.2507G>A",
"hgvs_p": "p.Arg836His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000618040.1",
"strand": true,
"transcript": "ENST00000947981.1",
"transcript_support_level": null
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1276,
"aa_ref": "R",
"aa_start": 836,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5308,
"cdna_start": 2760,
"cds_end": null,
"cds_length": 3831,
"cds_start": 2507,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_count": 34,
"exon_rank": 24,
"exon_rank_end": null,
"feature": "ENST00000927896.1",
"gene_hgnc_id": 7605,
"gene_symbol": "MYO6",
"hgvs_c": "c.2507G>A",
"hgvs_p": "p.Arg836His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000597955.1",
"strand": true,
"transcript": "ENST00000927896.1",
"transcript_support_level": null
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1275,
"aa_ref": "R",
"aa_start": 836,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5307,
"cdna_start": 2767,
"cds_end": null,
"cds_length": 3828,
"cds_start": 2507,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_count": 34,
"exon_rank": 24,
"exon_rank_end": null,
"feature": "ENST00000927895.1",
"gene_hgnc_id": 7605,
"gene_symbol": "MYO6",
"hgvs_c": "c.2507G>A",
"hgvs_p": "p.Arg836His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000597954.1",
"strand": true,
"transcript": "ENST00000927895.1",
"transcript_support_level": null
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1272,
"aa_ref": "R",
"aa_start": 836,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8576,
"cdna_start": 2739,
"cds_end": null,
"cds_length": 3819,
"cds_start": 2507,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_count": 34,
"exon_rank": 24,
"exon_rank_end": null,
"feature": "NM_001368137.1",
"gene_hgnc_id": 7605,
"gene_symbol": "MYO6",
"hgvs_c": "c.2507G>A",
"hgvs_p": "p.Arg836His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001355066.1",
"strand": true,
"transcript": "NM_001368137.1",
"transcript_support_level": null
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1272,
"aa_ref": "R",
"aa_start": 836,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5216,
"cdna_start": 2689,
"cds_end": null,
"cds_length": 3819,
"cds_start": 2507,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_count": 34,
"exon_rank": 24,
"exon_rank_end": null,
"feature": "ENST00000947980.1",
"gene_hgnc_id": 7605,
"gene_symbol": "MYO6",
"hgvs_c": "c.2507G>A",
"hgvs_p": "p.Arg836His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000618039.1",
"strand": true,
"transcript": "ENST00000947980.1",
"transcript_support_level": null
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1266,
"aa_ref": "R",
"aa_start": 836,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5698,
"cdna_start": 2803,
"cds_end": null,
"cds_length": 3801,
"cds_start": 2507,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_count": 33,
"exon_rank": 24,
"exon_rank_end": null,
"feature": "ENST00000927894.1",
"gene_hgnc_id": 7605,
"gene_symbol": "MYO6",
"hgvs_c": "c.2507G>A",
"hgvs_p": "p.Arg836His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000597953.1",
"strand": true,
"transcript": "ENST00000927894.1",
"transcript_support_level": null
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1263,
"aa_ref": "R",
"aa_start": 836,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8572,
"cdna_start": 2768,
"cds_end": null,
"cds_length": 3792,
"cds_start": 2507,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_count": 33,
"exon_rank": 24,
"exon_rank_end": null,
"feature": "ENST00000927893.1",
"gene_hgnc_id": 7605,
"gene_symbol": "MYO6",
"hgvs_c": "c.2507G>A",
"hgvs_p": "p.Arg836His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000597952.1",
"strand": true,
"transcript": "ENST00000927893.1",
"transcript_support_level": null
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1262,
"aa_ref": "R",
"aa_start": 836,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8546,
"cdna_start": 2739,
"cds_end": null,
"cds_length": 3789,
"cds_start": 2507,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_count": 33,
"exon_rank": 24,
"exon_rank_end": null,
"feature": "NM_001300899.2",
"gene_hgnc_id": 7605,
"gene_symbol": "MYO6",
"hgvs_c": "c.2507G>A",
"hgvs_p": "p.Arg836His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001287828.1",
"strand": true,
"transcript": "NM_001300899.2",
"transcript_support_level": null
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1262,
"aa_ref": "R",
"aa_start": 836,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8546,
"cdna_start": 2739,
"cds_end": null,
"cds_length": 3789,
"cds_start": 2507,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_count": 33,
"exon_rank": 24,
"exon_rank_end": null,
"feature": "ENST00000369985.9",
"gene_hgnc_id": 7605,
"gene_symbol": "MYO6",
"hgvs_c": "c.2507G>A",
"hgvs_p": "p.Arg836His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000359002.3",
"strand": true,
"transcript": "ENST00000369985.9",
"transcript_support_level": 5
},
{
"aa_alt": "H",
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"aa_length": 1257,
"aa_ref": "R",
"aa_start": 831,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8531,
"cdna_start": 2724,
"cds_end": null,
"cds_length": 3774,
"cds_start": 2492,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_count": 33,
"exon_rank": 24,
"exon_rank_end": null,
"feature": "NM_001368138.1",
"gene_hgnc_id": 7605,
"gene_symbol": "MYO6",
"hgvs_c": "c.2492G>A",
"hgvs_p": "p.Arg831His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001355067.1",
"strand": true,
"transcript": "NM_001368138.1",
"transcript_support_level": null
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1253,
"aa_ref": "R",
"aa_start": 836,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 8519,
"cdna_start": 2739,
"cds_end": null,
"cds_length": 3762,
"cds_start": 2507,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_count": 32,
"exon_rank": 24,
"exon_rank_end": null,
"feature": "NM_001368136.1",
"gene_hgnc_id": 7605,
"gene_symbol": "MYO6",
"hgvs_c": "c.2507G>A",
"hgvs_p": "p.Arg836His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001355065.1",
"strand": true,
"transcript": "NM_001368136.1",
"transcript_support_level": null
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1253,
"aa_ref": "R",
"aa_start": 836,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5598,
"cdna_start": 2743,
"cds_end": null,
"cds_length": 3762,
"cds_start": 2507,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_count": 32,
"exon_rank": 24,
"exon_rank_end": null,
"feature": "ENST00000369975.6",
"gene_hgnc_id": 7605,
"gene_symbol": "MYO6",
"hgvs_c": "c.2507G>A",
"hgvs_p": "p.Arg836His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000358992.1",
"strand": true,
"transcript": "ENST00000369975.6",
"transcript_support_level": 5
},
{
"aa_alt": "H",
"aa_end": null,
"aa_length": 1253,
"aa_ref": "R",
"aa_start": 836,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5194,
"cdna_start": 2720,
"cds_end": null,
"cds_length": 3762,
"cds_start": 2507,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_count": 32,
"exon_rank": 24,
"exon_rank_end": null,
"feature": "ENST00000927897.1",
"gene_hgnc_id": 7605,
"gene_symbol": "MYO6",
"hgvs_c": "c.2507G>A",
"hgvs_p": "p.Arg836His",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000597956.1",
"strand": true,
"transcript": "ENST00000927897.1",
"transcript_support_level": null
},
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},
{
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],
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"dbscsnv_ada_prediction": "Pathogenic",
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"dbsnp": "rs876657909",
"effect": "missense_variant,splice_region_variant",
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"pathogenicity_classification_combined": "Uncertain significance",
"phenotype_combined": "not specified",
"phylop100way_prediction": "Pathogenic",
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}
]
}