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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: 1-46562747-C-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=46562747&ref=C&alt=G&genome=hg38&allGenes=true"
API Response
json
{
"variants": [
{
"chr": "1",
"pos": 46562747,
"ref": "C",
"alt": "G",
"effect": "missense_variant",
"transcript": "ENST00000371945.10",
"consequences": [
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MKNK1",
"gene_hgnc_id": 7110,
"hgvs_c": "c.706G>C",
"hgvs_p": "p.Val236Leu",
"transcript": "NM_001135553.4",
"protein_id": "NP_001129025.2",
"transcript_support_level": null,
"aa_start": 236,
"aa_end": null,
"aa_length": 412,
"cds_start": 706,
"cds_end": null,
"cds_length": 1239,
"cdna_start": 960,
"cdna_end": null,
"cdna_length": 2661,
"mane_select": "ENST00000371945.10",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MKNK1",
"gene_hgnc_id": 7110,
"hgvs_c": "c.706G>C",
"hgvs_p": "p.Val236Leu",
"transcript": "ENST00000371945.10",
"protein_id": "ENSP00000361013.5",
"transcript_support_level": 1,
"aa_start": 236,
"aa_end": null,
"aa_length": 412,
"cds_start": 706,
"cds_end": null,
"cds_length": 1239,
"cdna_start": 960,
"cdna_end": null,
"cdna_length": 2661,
"mane_select": "NM_001135553.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MKNK1",
"gene_hgnc_id": 7110,
"hgvs_c": "c.829G>C",
"hgvs_p": "p.Val277Leu",
"transcript": "ENST00000371946.9",
"protein_id": "ENSP00000361014.5",
"transcript_support_level": 1,
"aa_start": 277,
"aa_end": null,
"aa_length": 453,
"cds_start": 829,
"cds_end": null,
"cds_length": 1362,
"cdna_start": 1029,
"cdna_end": null,
"cdna_length": 2719,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MKNK1",
"gene_hgnc_id": 7110,
"hgvs_c": "n.732G>C",
"hgvs_p": null,
"transcript": "ENST00000342571.7",
"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": 2422,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MKNK1",
"gene_hgnc_id": 7110,
"hgvs_c": "n.*473G>C",
"hgvs_p": null,
"transcript": "ENST00000531355.6",
"protein_id": "ENSP00000434493.2",
"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": 1121,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MKNK1",
"gene_hgnc_id": 7110,
"hgvs_c": "n.*473G>C",
"hgvs_p": null,
"transcript": "ENST00000531355.6",
"protein_id": "ENSP00000434493.2",
"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": 1121,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MKNK1",
"gene_hgnc_id": 7110,
"hgvs_c": "c.865G>C",
"hgvs_p": "p.Val289Leu",
"transcript": "ENST00000649800.1",
"protein_id": "ENSP00000498083.1",
"transcript_support_level": null,
"aa_start": 289,
"aa_end": null,
"aa_length": 465,
"cds_start": 865,
"cds_end": null,
"cds_length": 1398,
"cdna_start": 1109,
"cdna_end": null,
"cdna_length": 2809,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MKNK1",
"gene_hgnc_id": 7110,
"hgvs_c": "c.829G>C",
"hgvs_p": "p.Val277Leu",
"transcript": "NM_003684.7",
"protein_id": "NP_003675.3",
"transcript_support_level": null,
"aa_start": 277,
"aa_end": null,
"aa_length": 453,
"cds_start": 829,
"cds_end": null,
"cds_length": 1362,
"cdna_start": 1083,
"cdna_end": null,
"cdna_length": 2784,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MKNK1",
"gene_hgnc_id": 7110,
"hgvs_c": "c.742G>C",
"hgvs_p": "p.Val248Leu",
"transcript": "ENST00000650508.1",
"protein_id": "ENSP00000498143.1",
"transcript_support_level": null,
"aa_start": 248,
"aa_end": null,
"aa_length": 424,
"cds_start": 742,
"cds_end": null,
"cds_length": 1275,
"cdna_start": 986,
"cdna_end": null,
"cdna_length": 2686,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MKNK1",
"gene_hgnc_id": 7110,
"hgvs_c": "c.724G>C",
"hgvs_p": "p.Val242Leu",
"transcript": "NM_001377337.1",
"protein_id": "NP_001364266.1",
"transcript_support_level": null,
"aa_start": 242,
"aa_end": null,
"aa_length": 418,
"cds_start": 724,
"cds_end": null,
"cds_length": 1257,
"cdna_start": 1019,
"cdna_end": null,
"cdna_length": 2720,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MKNK1",
"gene_hgnc_id": 7110,
"hgvs_c": "c.724G>C",
"hgvs_p": "p.Val242Leu",
"transcript": "NM_001377338.1",
"protein_id": "NP_001364267.1",
"transcript_support_level": null,
"aa_start": 242,
"aa_end": null,
"aa_length": 418,
"cds_start": 724,
"cds_end": null,
"cds_length": 1257,
"cdna_start": 1061,
"cdna_end": null,
"cdna_length": 2762,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MKNK1",
"gene_hgnc_id": 7110,
"hgvs_c": "c.706G>C",
"hgvs_p": "p.Val236Leu",
"transcript": "NM_001377373.1",
"protein_id": "NP_001364302.1",
"transcript_support_level": null,
"aa_start": 236,
"aa_end": null,
"aa_length": 412,
"cds_start": 706,
"cds_end": null,
"cds_length": 1239,
"cdna_start": 918,
"cdna_end": null,
"cdna_length": 2619,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MKNK1",
"gene_hgnc_id": 7110,
"hgvs_c": "c.742G>C",
"hgvs_p": "p.Val248Leu",
"transcript": "ENST00000650026.1",
"protein_id": "ENSP00000497380.1",
"transcript_support_level": null,
"aa_start": 248,
"aa_end": null,
"aa_length": 347,
"cds_start": 742,
"cds_end": null,
"cds_length": 1044,
"cdna_start": 944,
"cdna_end": null,
"cdna_length": 2600,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MKNK1",
"gene_hgnc_id": 7110,
"hgvs_c": "c.724G>C",
"hgvs_p": "p.Val242Leu",
"transcript": "NM_001377341.1",
"protein_id": "NP_001364270.1",
"transcript_support_level": null,
"aa_start": 242,
"aa_end": null,
"aa_length": 341,
"cds_start": 724,
"cds_end": null,
"cds_length": 1026,
"cdna_start": 1019,
"cdna_end": null,
"cdna_length": 2676,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MKNK1",
"gene_hgnc_id": 7110,
"hgvs_c": "c.724G>C",
"hgvs_p": "p.Val242Leu",
"transcript": "NM_001377342.1",
"protein_id": "NP_001364271.1",
"transcript_support_level": null,
"aa_start": 242,
"aa_end": null,
"aa_length": 341,
"cds_start": 724,
"cds_end": null,
"cds_length": 1026,
"cdna_start": 1061,
"cdna_end": null,
"cdna_length": 2718,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MKNK1",
"gene_hgnc_id": 7110,
"hgvs_c": "c.706G>C",
"hgvs_p": "p.Val236Leu",
"transcript": "NM_001377374.1",
"protein_id": "NP_001364303.1",
"transcript_support_level": null,
"aa_start": 236,
"aa_end": null,
"aa_length": 335,
"cds_start": 706,
"cds_end": null,
"cds_length": 1008,
"cdna_start": 960,
"cdna_end": null,
"cdna_length": 2617,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MKNK1",
"gene_hgnc_id": 7110,
"hgvs_c": "c.706G>C",
"hgvs_p": "p.Val236Leu",
"transcript": "NM_001377375.1",
"protein_id": "NP_001364304.1",
"transcript_support_level": null,
"aa_start": 236,
"aa_end": null,
"aa_length": 335,
"cds_start": 706,
"cds_end": null,
"cds_length": 1008,
"cdna_start": 980,
"cdna_end": null,
"cdna_length": 2637,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MKNK1",
"gene_hgnc_id": 7110,
"hgvs_c": "c.706G>C",
"hgvs_p": "p.Val236Leu",
"transcript": "NM_198973.5",
"protein_id": "NP_945324.2",
"transcript_support_level": null,
"aa_start": 236,
"aa_end": null,
"aa_length": 335,
"cds_start": 706,
"cds_end": null,
"cds_length": 1008,
"cdna_start": 918,
"cdna_end": null,
"cdna_length": 2575,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MKNK1",
"gene_hgnc_id": 7110,
"hgvs_c": "c.706G>C",
"hgvs_p": "p.Val236Leu",
"transcript": "ENST00000428112.7",
"protein_id": "ENSP00000411135.3",
"transcript_support_level": 2,
"aa_start": 236,
"aa_end": null,
"aa_length": 335,
"cds_start": 706,
"cds_end": null,
"cds_length": 1008,
"cdna_start": 905,
"cdna_end": null,
"cdna_length": 1270,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MKNK1",
"gene_hgnc_id": 7110,
"hgvs_c": "c.457G>C",
"hgvs_p": "p.Val153Leu",
"transcript": "ENST00000341183.9",
"protein_id": "ENSP00000339573.6",
"transcript_support_level": 5,
"aa_start": 153,
"aa_end": null,
"aa_length": 329,
"cds_start": 457,
"cds_end": null,
"cds_length": 990,
"cdna_start": 912,
"cdna_end": null,
"cdna_length": 2612,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MKNK1",
"gene_hgnc_id": 7110,
"hgvs_c": "c.577G>C",
"hgvs_p": "p.Val193Leu",
"transcript": "NM_001377343.1",
"protein_id": "NP_001364272.1",
"transcript_support_level": null,
"aa_start": 193,
"aa_end": null,
"aa_length": 292,
"cds_start": 577,
"cds_end": null,
"cds_length": 879,
"cdna_start": 820,
"cdna_end": null,
"cdna_length": 2477,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MKNK1",
"gene_hgnc_id": 7110,
"hgvs_c": "c.118G>C",
"hgvs_p": "p.Val40Leu",
"transcript": "ENST00000524749.5",
"protein_id": "ENSP00000435069.1",
"transcript_support_level": 5,
"aa_start": 40,
"aa_end": null,
"aa_length": 84,
"cds_start": 118,
"cds_end": null,
"cds_length": 255,
"cdna_start": 120,
"cdna_end": null,
"cdna_length": 786,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MKNK1",
"gene_hgnc_id": 7110,
"hgvs_c": "c.751G>C",
"hgvs_p": "p.Val251Leu",
"transcript": "XM_047433022.1",
"protein_id": "XP_047288978.1",
"transcript_support_level": null,
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}
],
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"computational_prediction_selected": "Pathogenic",
"computational_source_selected": "MetaRNN",
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"splice_prediction_selected": "Benign",
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"bayesdelnoaf_score": 0.1,
"bayesdelnoaf_prediction": "Uncertain_significance",
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"phylop100way_prediction": "Pathogenic",
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"spliceai_max_prediction": "Benign",
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"acmg_classification": "Uncertain_significance",
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"acmg_by_gene": [
{
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"PP3_Moderate"
],
"verdict": "Uncertain_significance",
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"effects": [
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"inheritance_mode": "AR",
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{
"score": 4,
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"PP3_Moderate"
],
"verdict": "Uncertain_significance",
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"effects": [
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],
"inheritance_mode": "",
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}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}