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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: 2-73938978-C-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=73938978&ref=C&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 73938978,
"ref": "C",
"alt": "G",
"effect": "missense_variant",
"transcript": "NM_080916.3",
"consequences": [
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DGUOK",
"gene_hgnc_id": 2858,
"hgvs_c": "c.211C>G",
"hgvs_p": "p.Pro71Ala",
"transcript": "NM_080916.3",
"protein_id": "NP_550438.1",
"transcript_support_level": null,
"aa_start": 71,
"aa_end": null,
"aa_length": 277,
"cds_start": 211,
"cds_end": null,
"cds_length": 834,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000264093.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_080916.3"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DGUOK",
"gene_hgnc_id": 2858,
"hgvs_c": "c.211C>G",
"hgvs_p": "p.Pro71Ala",
"transcript": "ENST00000264093.9",
"protein_id": "ENSP00000264093.4",
"transcript_support_level": 1,
"aa_start": 71,
"aa_end": null,
"aa_length": 277,
"cds_start": 211,
"cds_end": null,
"cds_length": 834,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_080916.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000264093.9"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "DGUOK",
"gene_hgnc_id": 2858,
"hgvs_c": "n.143-7741C>G",
"hgvs_p": null,
"transcript": "ENST00000418996.5",
"protein_id": "ENSP00000408209.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000418996.5"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DGUOK",
"gene_hgnc_id": 2858,
"hgvs_c": "c.211C>G",
"hgvs_p": "p.Pro71Ala",
"transcript": "ENST00000893377.1",
"protein_id": "ENSP00000563436.1",
"transcript_support_level": null,
"aa_start": 71,
"aa_end": null,
"aa_length": 271,
"cds_start": 211,
"cds_end": null,
"cds_length": 816,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000893377.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DGUOK",
"gene_hgnc_id": 2858,
"hgvs_c": "c.211C>G",
"hgvs_p": "p.Pro71Ala",
"transcript": "ENST00000893380.1",
"protein_id": "ENSP00000563439.1",
"transcript_support_level": null,
"aa_start": 71,
"aa_end": null,
"aa_length": 263,
"cds_start": 211,
"cds_end": null,
"cds_length": 792,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000893380.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DGUOK",
"gene_hgnc_id": 2858,
"hgvs_c": "c.211C>G",
"hgvs_p": "p.Pro71Ala",
"transcript": "NM_080918.3",
"protein_id": "NP_550440.1",
"transcript_support_level": null,
"aa_start": 71,
"aa_end": null,
"aa_length": 189,
"cds_start": 211,
"cds_end": null,
"cds_length": 570,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_080918.3"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DGUOK",
"gene_hgnc_id": 2858,
"hgvs_c": "c.211C>G",
"hgvs_p": "p.Pro71Ala",
"transcript": "ENST00000348222.3",
"protein_id": "ENSP00000306964.3",
"transcript_support_level": 2,
"aa_start": 71,
"aa_end": null,
"aa_length": 189,
"cds_start": 211,
"cds_end": null,
"cds_length": 570,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000348222.3"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DGUOK",
"gene_hgnc_id": 2858,
"hgvs_c": "c.211C>G",
"hgvs_p": "p.Pro71Ala",
"transcript": "NM_001318859.2",
"protein_id": "NP_001305788.1",
"transcript_support_level": null,
"aa_start": 71,
"aa_end": null,
"aa_length": 183,
"cds_start": 211,
"cds_end": null,
"cds_length": 552,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001318859.2"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DGUOK",
"gene_hgnc_id": 2858,
"hgvs_c": "c.211C>G",
"hgvs_p": "p.Pro71Ala",
"transcript": "ENST00000893378.1",
"protein_id": "ENSP00000563437.1",
"transcript_support_level": null,
"aa_start": 71,
"aa_end": null,
"aa_length": 183,
"cds_start": 211,
"cds_end": null,
"cds_length": 552,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000893378.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DGUOK",
"gene_hgnc_id": 2858,
"hgvs_c": "c.211C>G",
"hgvs_p": "p.Pro71Ala",
"transcript": "ENST00000893379.1",
"protein_id": "ENSP00000563438.1",
"transcript_support_level": null,
"aa_start": 71,
"aa_end": null,
"aa_length": 165,
"cds_start": 211,
"cds_end": null,
"cds_length": 498,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000893379.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DGUOK",
"gene_hgnc_id": 2858,
"hgvs_c": "c.211C>G",
"hgvs_p": "p.Pro71Ala",
"transcript": "XM_011532647.3",
"protein_id": "XP_011530949.1",
"transcript_support_level": null,
"aa_start": 71,
"aa_end": null,
"aa_length": 271,
"cds_start": 211,
"cds_end": null,
"cds_length": 816,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011532647.3"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DGUOK",
"gene_hgnc_id": 2858,
"hgvs_c": "c.211C>G",
"hgvs_p": "p.Pro71Ala",
"transcript": "XM_047443585.1",
"protein_id": "XP_047299541.1",
"transcript_support_level": null,
"aa_start": 71,
"aa_end": null,
"aa_length": 200,
"cds_start": 211,
"cds_end": null,
"cds_length": 603,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047443585.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DGUOK",
"gene_hgnc_id": 2858,
"hgvs_c": "c.211C>G",
"hgvs_p": "p.Pro71Ala",
"transcript": "XM_047443587.1",
"protein_id": "XP_047299543.1",
"transcript_support_level": null,
"aa_start": 71,
"aa_end": null,
"aa_length": 165,
"cds_start": 211,
"cds_end": null,
"cds_length": 498,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047443587.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "DGUOK",
"gene_hgnc_id": 2858,
"hgvs_c": "c.-36-7741C>G",
"hgvs_p": null,
"transcript": "NM_001318860.2",
"protein_id": "NP_001305789.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 180,
"cds_start": null,
"cds_end": null,
"cds_length": 543,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001318860.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "DGUOK",
"gene_hgnc_id": 2858,
"hgvs_c": "c.-37+6295C>G",
"hgvs_p": null,
"transcript": "NM_001318861.2",
"protein_id": "NP_001305790.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 180,
"cds_start": null,
"cds_end": null,
"cds_length": 543,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001318861.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "DGUOK",
"gene_hgnc_id": 2858,
"hgvs_c": "c.-37+6295C>G",
"hgvs_p": null,
"transcript": "NM_001318862.2",
"protein_id": "NP_001305791.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 174,
"cds_start": null,
"cds_end": null,
"cds_length": 525,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001318862.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "DGUOK",
"gene_hgnc_id": 2858,
"hgvs_c": "c.-36-7741C>G",
"hgvs_p": null,
"transcript": "NM_001318863.2",
"protein_id": "NP_001305792.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 174,
"cds_start": null,
"cds_end": null,
"cds_length": 525,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001318863.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "DGUOK",
"gene_hgnc_id": 2858,
"hgvs_c": "c.143-11607C>G",
"hgvs_p": null,
"transcript": "ENST00000893381.1",
"protein_id": "ENSP00000563440.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 138,
"cds_start": null,
"cds_end": null,
"cds_length": 417,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000893381.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "DGUOK",
"gene_hgnc_id": 2858,
"hgvs_c": "c.143-11649C>G",
"hgvs_p": null,
"transcript": "ENST00000915418.1",
"protein_id": "ENSP00000585477.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 124,
"cds_start": null,
"cds_end": null,
"cds_length": 375,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000915418.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "DGUOK",
"gene_hgnc_id": 2858,
"hgvs_c": "c.133+11935C>G",
"hgvs_p": null,
"transcript": "ENST00000915416.1",
"protein_id": "ENSP00000585475.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 109,
"cds_start": null,
"cds_end": null,
"cds_length": 330,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000915416.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "DGUOK",
"gene_hgnc_id": 2858,
"hgvs_c": "c.142+11926C>G",
"hgvs_p": null,
"transcript": "ENST00000915417.1",
"protein_id": "ENSP00000585476.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 104,
"cds_start": null,
"cds_end": null,
"cds_length": 315,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000915417.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DGUOK",
"gene_hgnc_id": 2858,
"hgvs_c": "n.228C>G",
"hgvs_p": null,
"transcript": "ENST00000489796.5",
"protein_id": null,
"transcript_support_level": 3,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000489796.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
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"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
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"revel_prediction": "Pathogenic",
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"bayesdelnoaf_score": 0.49,
"bayesdelnoaf_prediction": "Pathogenic",
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"phylop100way_prediction": "Uncertain_significance",
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"acmg_score": -8,
"acmg_classification": "Benign",
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{
"score": -8,
"benign_score": 9,
"pathogenic_score": 1,
"criteria": [
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"BP4_Strong",
"BS1_Supporting",
"BS2"
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"verdict": "Benign",
"transcript": "NM_080916.3",
"gene_symbol": "DGUOK",
"hgnc_id": 2858,
"effects": [
"missense_variant"
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"inheritance_mode": "AR",
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"hgvs_p": "p.Pro71Ala"
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{
"score": -7,
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"pathogenic_score": 1,
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"BP4_Strong",
"BS2"
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"verdict": "Benign",
"transcript": "ENST00000804860.1",
"gene_symbol": "DGUOK-AS1",
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"effects": [
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],
"inheritance_mode": "",
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"clinvar_disease": " 1, autosomal recessive 4, noncirrhotic,DGUOK-related disorder,Inborn genetic diseases,Mitochondrial DNA depletion syndrome 3 (hepatocerebral type),Mitochondrial disease,Portal hypertension,Progressive external ophthalmoplegia with mitochondrial DNA deletions,not provided,not specified",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "US:8",
"phenotype_combined": "Inborn genetic diseases|not specified|not provided|Mitochondrial disease|Mitochondrial DNA depletion syndrome 3 (hepatocerebral type);Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4;Portal hypertension, noncirrhotic, 1|DGUOK-related disorder",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}