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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: 2-170369229-A-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=170369229&ref=A&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 170369229,
"ref": "A",
"alt": "G",
"effect": "missense_variant",
"transcript": "NM_138995.5",
"consequences": [
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 35,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "c.823A>G",
"hgvs_p": "p.Ile275Val",
"transcript": "NM_138995.5",
"protein_id": "NP_620482.3",
"transcript_support_level": null,
"aa_start": 275,
"aa_end": null,
"aa_length": 1341,
"cds_start": 823,
"cds_end": null,
"cds_length": 4026,
"cdna_start": 964,
"cdna_end": null,
"cdna_length": 6213,
"mane_select": "ENST00000408978.9",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 35,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "c.823A>G",
"hgvs_p": "p.Ile275Val",
"transcript": "ENST00000408978.9",
"protein_id": "ENSP00000386213.4",
"transcript_support_level": 1,
"aa_start": 275,
"aa_end": null,
"aa_length": 1341,
"cds_start": 823,
"cds_end": null,
"cds_length": 4026,
"cdna_start": 964,
"cdna_end": null,
"cdna_length": 6213,
"mane_select": "NM_138995.5",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 34,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "c.823A>G",
"hgvs_p": "p.Ile275Val",
"transcript": "ENST00000409044.7",
"protein_id": "ENSP00000386497.3",
"transcript_support_level": 1,
"aa_start": 275,
"aa_end": null,
"aa_length": 1314,
"cds_start": 823,
"cds_end": null,
"cds_length": 3945,
"cdna_start": 966,
"cdna_end": null,
"cdna_length": 5448,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "c.820A>G",
"hgvs_p": "p.Ile274Val",
"transcript": "ENST00000442690.1",
"protein_id": "ENSP00000401160.1",
"transcript_support_level": 1,
"aa_start": 274,
"aa_end": null,
"aa_length": 359,
"cds_start": 820,
"cds_end": null,
"cds_length": 1080,
"cdna_start": 821,
"cdna_end": null,
"cdna_length": 1720,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 30,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "n.966A>G",
"hgvs_p": null,
"transcript": "ENST00000409940.6",
"protein_id": null,
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4156,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"5_prime_UTR_premature_start_codon_gain_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "c.-159A>G",
"hgvs_p": null,
"transcript": "XM_011510657.4",
"protein_id": "XP_011508959.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1050,
"cds_start": -4,
"cds_end": null,
"cds_length": 3153,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5430,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"5_prime_UTR_premature_start_codon_gain_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "c.-159A>G",
"hgvs_p": null,
"transcript": "XM_024452713.2",
"protein_id": "XP_024308481.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1050,
"cds_start": -4,
"cds_end": null,
"cds_length": 3153,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5623,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 34,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "c.823A>G",
"hgvs_p": "p.Ile275Val",
"transcript": "NM_001083615.4",
"protein_id": "NP_001077084.2",
"transcript_support_level": null,
"aa_start": 275,
"aa_end": null,
"aa_length": 1314,
"cds_start": 823,
"cds_end": null,
"cds_length": 3945,
"cdna_start": 964,
"cdna_end": null,
"cdna_length": 6132,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "c.850A>G",
"hgvs_p": "p.Ile284Val",
"transcript": "ENST00000484338.6",
"protein_id": "ENSP00000446237.1",
"transcript_support_level": 5,
"aa_start": 284,
"aa_end": null,
"aa_length": 1104,
"cds_start": 850,
"cds_end": null,
"cds_length": 3316,
"cdna_start": 854,
"cdna_end": null,
"cdna_length": 3320,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "c.850A>G",
"hgvs_p": "p.Ile284Val",
"transcript": "XM_011510654.4",
"protein_id": "XP_011508956.1",
"transcript_support_level": null,
"aa_start": 284,
"aa_end": null,
"aa_length": 1386,
"cds_start": 850,
"cds_end": null,
"cds_length": 4161,
"cdna_start": 873,
"cdna_end": null,
"cdna_length": 6230,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 35,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "c.850A>G",
"hgvs_p": "p.Ile284Val",
"transcript": "XM_006712299.5",
"protein_id": "XP_006712362.1",
"transcript_support_level": null,
"aa_start": 284,
"aa_end": null,
"aa_length": 1350,
"cds_start": 850,
"cds_end": null,
"cds_length": 4053,
"cdna_start": 873,
"cdna_end": null,
"cdna_length": 6122,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 34,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "c.850A>G",
"hgvs_p": "p.Ile284Val",
"transcript": "XM_011510655.4",
"protein_id": "XP_011508957.1",
"transcript_support_level": null,
"aa_start": 284,
"aa_end": null,
"aa_length": 1323,
"cds_start": 850,
"cds_end": null,
"cds_length": 3972,
"cdna_start": 873,
"cdna_end": null,
"cdna_length": 6041,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 30,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "c.13A>G",
"hgvs_p": "p.Ile5Val",
"transcript": "XM_011510656.4",
"protein_id": "XP_011508958.1",
"transcript_support_level": null,
"aa_start": 5,
"aa_end": null,
"aa_length": 1155,
"cds_start": 13,
"cds_end": null,
"cds_length": 3468,
"cdna_start": 85,
"cdna_end": null,
"cdna_length": 5586,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 35,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "n.823A>G",
"hgvs_p": null,
"transcript": "ENST00000317935.10",
"protein_id": "ENSP00000314650.6",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5479,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 34,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "n.966A>G",
"hgvs_p": null,
"transcript": "ENST00000438642.6",
"protein_id": null,
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4010,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "n.691A>G",
"hgvs_p": null,
"transcript": "ENST00000602629.1",
"protein_id": null,
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
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"cdna_length": 5304,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "n.964A>G",
"hgvs_p": null,
"transcript": "NR_045682.2",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 6335,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "n.964A>G",
"hgvs_p": null,
"transcript": "NR_045683.2",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 6244,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 35,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "n.964A>G",
"hgvs_p": null,
"transcript": "NR_045684.2",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
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"cdna_start": null,
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"cdna_length": 6163,
"mane_select": null,
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"biotype": null,
"feature": null
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"5_prime_UTR_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "c.-159A>G",
"hgvs_p": null,
"transcript": "XM_011510657.4",
"protein_id": "XP_011508959.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1050,
"cds_start": -4,
"cds_end": null,
"cds_length": 3153,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5430,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"5_prime_UTR_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "c.-159A>G",
"hgvs_p": null,
"transcript": "XM_024452713.2",
"protein_id": "XP_024308481.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1050,
"cds_start": -4,
"cds_end": null,
"cds_length": 3153,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5623,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "MYO3B-AS1",
"gene_hgnc_id": 40713,
"hgvs_c": "n.196+14598T>C",
"hgvs_p": null,
"transcript": "ENST00000625968.2",
"protein_id": null,
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 763,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"dbsnp": "rs10209102",
"frequency_reference_population": 0.0019450018,
"hom_count_reference_population": 51,
"allele_count_reference_population": 3137,
"gnomad_exomes_af": 0.00110844,
"gnomad_genomes_af": 0.00997097,
"gnomad_exomes_ac": 1619,
"gnomad_genomes_ac": 1518,
"gnomad_exomes_homalt": 30,
"gnomad_genomes_homalt": 21,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.008387088775634766,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.256,
"revel_prediction": "Benign",
"alphamissense_score": 0.1053,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.37,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 7.248,
"phylop100way_prediction": "Uncertain_significance",
"spliceai_max_score": 0,
"spliceai_max_prediction": "Benign",
"dbscsnv_ada_score": null,
"dbscsnv_ada_prediction": null,
"apogee2_score": null,
"apogee2_prediction": null,
"mitotip_score": null,
"mitotip_prediction": null,
"acmg_score": -20,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6_Very_Strong,BS1,BS2",
"acmg_by_gene": [
{
"score": -20,
"benign_score": 20,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong",
"BS1",
"BS2"
],
"verdict": "Benign",
"transcript": "NM_138995.5",
"gene_symbol": "MYO3B",
"hgnc_id": 15576,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.823A>G",
"hgvs_p": "p.Ile275Val"
},
{
"score": -20,
"benign_score": 20,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong",
"BS1",
"BS2"
],
"verdict": "Benign",
"transcript": "ENST00000625968.2",
"gene_symbol": "MYO3B-AS1",
"hgnc_id": 40713,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.196+14598T>C",
"hgvs_p": null
}
],
"clinvar_disease": "not provided",
"clinvar_classification": "Benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "B:2",
"phenotype_combined": "not provided",
"pathogenicity_classification_combined": "Benign",
"custom_annotations": null
}
],
"message": null
}