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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: 1-183232835-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=183232835&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "1",
"pos": 183232835,
"ref": "G",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_005562.3",
"consequences": [
{
"aa_ref": "S",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LAMC2",
"gene_hgnc_id": 6493,
"hgvs_c": "c.2198G>C",
"hgvs_p": "p.Ser733Thr",
"transcript": "NM_005562.3",
"protein_id": "NP_005553.2",
"transcript_support_level": null,
"aa_start": 733,
"aa_end": null,
"aa_length": 1193,
"cds_start": 2198,
"cds_end": null,
"cds_length": 3582,
"cdna_start": 2287,
"cdna_end": null,
"cdna_length": 5398,
"mane_select": "ENST00000264144.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_005562.3"
},
{
"aa_ref": "S",
"aa_alt": "T",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LAMC2",
"gene_hgnc_id": 6493,
"hgvs_c": "c.2198G>C",
"hgvs_p": "p.Ser733Thr",
"transcript": "ENST00000264144.5",
"protein_id": "ENSP00000264144.4",
"transcript_support_level": 1,
"aa_start": 733,
"aa_end": null,
"aa_length": 1193,
"cds_start": 2198,
"cds_end": null,
"cds_length": 3582,
"cdna_start": 2287,
"cdna_end": null,
"cdna_length": 5398,
"mane_select": "NM_005562.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000264144.5"
},
{
"aa_ref": "S",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LAMC2",
"gene_hgnc_id": 6493,
"hgvs_c": "c.2198G>C",
"hgvs_p": "p.Ser733Thr",
"transcript": "ENST00000493293.5",
"protein_id": "ENSP00000432063.1",
"transcript_support_level": 1,
"aa_start": 733,
"aa_end": null,
"aa_length": 1111,
"cds_start": 2198,
"cds_end": null,
"cds_length": 3336,
"cdna_start": 2313,
"cdna_end": null,
"cdna_length": 4313,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000493293.5"
},
{
"aa_ref": "S",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LAMC2",
"gene_hgnc_id": 6493,
"hgvs_c": "c.2222G>C",
"hgvs_p": "p.Ser741Thr",
"transcript": "ENST00000914499.1",
"protein_id": "ENSP00000584558.1",
"transcript_support_level": null,
"aa_start": 741,
"aa_end": null,
"aa_length": 1201,
"cds_start": 2222,
"cds_end": null,
"cds_length": 3606,
"cdna_start": 2262,
"cdna_end": null,
"cdna_length": 4808,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000914499.1"
},
{
"aa_ref": "S",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LAMC2",
"gene_hgnc_id": 6493,
"hgvs_c": "c.2075G>C",
"hgvs_p": "p.Ser692Thr",
"transcript": "ENST00000878927.1",
"protein_id": "ENSP00000548986.1",
"transcript_support_level": null,
"aa_start": 692,
"aa_end": null,
"aa_length": 1152,
"cds_start": 2075,
"cds_end": null,
"cds_length": 3459,
"cdna_start": 2201,
"cdna_end": null,
"cdna_length": 4733,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000878927.1"
},
{
"aa_ref": "S",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LAMC2",
"gene_hgnc_id": 6493,
"hgvs_c": "c.2072G>C",
"hgvs_p": "p.Ser691Thr",
"transcript": "ENST00000878928.1",
"protein_id": "ENSP00000548987.1",
"transcript_support_level": null,
"aa_start": 691,
"aa_end": null,
"aa_length": 1151,
"cds_start": 2072,
"cds_end": null,
"cds_length": 3456,
"cdna_start": 2174,
"cdna_end": null,
"cdna_length": 4720,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000878928.1"
},
{
"aa_ref": "S",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LAMC2",
"gene_hgnc_id": 6493,
"hgvs_c": "c.2009G>C",
"hgvs_p": "p.Ser670Thr",
"transcript": "ENST00000878925.1",
"protein_id": "ENSP00000548984.1",
"transcript_support_level": null,
"aa_start": 670,
"aa_end": null,
"aa_length": 1130,
"cds_start": 2009,
"cds_end": null,
"cds_length": 3393,
"cdna_start": 2127,
"cdna_end": null,
"cdna_length": 5007,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000878925.1"
},
{
"aa_ref": "S",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LAMC2",
"gene_hgnc_id": 6493,
"hgvs_c": "c.1979G>C",
"hgvs_p": "p.Ser660Thr",
"transcript": "ENST00000971656.1",
"protein_id": "ENSP00000641715.1",
"transcript_support_level": null,
"aa_start": 660,
"aa_end": null,
"aa_length": 1120,
"cds_start": 1979,
"cds_end": null,
"cds_length": 3363,
"cdna_start": 2275,
"cdna_end": null,
"cdna_length": 4816,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000971656.1"
},
{
"aa_ref": "S",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LAMC2",
"gene_hgnc_id": 6493,
"hgvs_c": "c.2198G>C",
"hgvs_p": "p.Ser733Thr",
"transcript": "NM_018891.3",
"protein_id": "NP_061486.2",
"transcript_support_level": null,
"aa_start": 733,
"aa_end": null,
"aa_length": 1111,
"cds_start": 2198,
"cds_end": null,
"cds_length": 3336,
"cdna_start": 2287,
"cdna_end": null,
"cdna_length": 4320,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_018891.3"
},
{
"aa_ref": "S",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LAMC2",
"gene_hgnc_id": 6493,
"hgvs_c": "c.1952G>C",
"hgvs_p": "p.Ser651Thr",
"transcript": "ENST00000878926.1",
"protein_id": "ENSP00000548985.1",
"transcript_support_level": null,
"aa_start": 651,
"aa_end": null,
"aa_length": 1111,
"cds_start": 1952,
"cds_end": null,
"cds_length": 3336,
"cdna_start": 2064,
"cdna_end": null,
"cdna_length": 4610,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000878926.1"
},
{
"aa_ref": "S",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LAMC2",
"gene_hgnc_id": 6493,
"hgvs_c": "c.1910G>C",
"hgvs_p": "p.Ser637Thr",
"transcript": "ENST00000914498.1",
"protein_id": "ENSP00000584557.1",
"transcript_support_level": null,
"aa_start": 637,
"aa_end": null,
"aa_length": 1097,
"cds_start": 1910,
"cds_end": null,
"cds_length": 3294,
"cdna_start": 2100,
"cdna_end": null,
"cdna_length": 4646,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000914498.1"
},
{
"aa_ref": "S",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LAMC2",
"gene_hgnc_id": 6493,
"hgvs_c": "c.1763G>C",
"hgvs_p": "p.Ser588Thr",
"transcript": "ENST00000971655.1",
"protein_id": "ENSP00000641714.1",
"transcript_support_level": null,
"aa_start": 588,
"aa_end": null,
"aa_length": 1048,
"cds_start": 1763,
"cds_end": null,
"cds_length": 3147,
"cdna_start": 1900,
"cdna_end": null,
"cdna_length": 4783,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000971655.1"
},
{
"aa_ref": "S",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LAMC2",
"gene_hgnc_id": 6493,
"hgvs_c": "c.1649G>C",
"hgvs_p": "p.Ser550Thr",
"transcript": "ENST00000971657.1",
"protein_id": "ENSP00000641716.1",
"transcript_support_level": null,
"aa_start": 550,
"aa_end": null,
"aa_length": 1010,
"cds_start": 1649,
"cds_end": null,
"cds_length": 3033,
"cdna_start": 1739,
"cdna_end": null,
"cdna_length": 4282,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000971657.1"
},
{
"aa_ref": "S",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LAMC2",
"gene_hgnc_id": 6493,
"hgvs_c": "c.2198G>C",
"hgvs_p": "p.Ser733Thr",
"transcript": "XM_047420358.1",
"protein_id": "XP_047276314.1",
"transcript_support_level": null,
"aa_start": 733,
"aa_end": null,
"aa_length": 1191,
"cds_start": 2198,
"cds_end": null,
"cds_length": 3576,
"cdna_start": 2287,
"cdna_end": null,
"cdna_length": 3691,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047420358.1"
},
{
"aa_ref": "S",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LAMC2",
"gene_hgnc_id": 6493,
"hgvs_c": "c.2198G>C",
"hgvs_p": "p.Ser733Thr",
"transcript": "XM_047420361.1",
"protein_id": "XP_047276317.1",
"transcript_support_level": null,
"aa_start": 733,
"aa_end": null,
"aa_length": 1182,
"cds_start": 2198,
"cds_end": null,
"cds_length": 3549,
"cdna_start": 2287,
"cdna_end": null,
"cdna_length": 3664,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047420361.1"
},
{
"aa_ref": "S",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LAMC2",
"gene_hgnc_id": 6493,
"hgvs_c": "c.2198G>C",
"hgvs_p": "p.Ser733Thr",
"transcript": "XM_017001273.2",
"protein_id": "XP_016856762.1",
"transcript_support_level": null,
"aa_start": 733,
"aa_end": null,
"aa_length": 742,
"cds_start": 2198,
"cds_end": null,
"cds_length": 2229,
"cdna_start": 2287,
"cdna_end": null,
"cdna_length": 2403,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017001273.2"
}
],
"gene_symbol": "LAMC2",
"gene_hgnc_id": 6493,
"dbsnp": "rs2296303",
"frequency_reference_population": 0.1418677,
"hom_count_reference_population": 17375,
"allele_count_reference_population": 228937,
"gnomad_exomes_af": 0.13987,
"gnomad_genomes_af": 0.161066,
"gnomad_exomes_ac": 204435,
"gnomad_genomes_ac": 24502,
"gnomad_exomes_homalt": 15226,
"gnomad_genomes_homalt": 2149,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.0030424296855926514,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.019999999552965164,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.066,
"revel_prediction": "Benign",
"alphamissense_score": 0.0971,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.69,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 1.304,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0.02,
"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,BA1",
"acmg_by_gene": [
{
"score": -20,
"benign_score": 20,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong",
"BA1"
],
"verdict": "Benign",
"transcript": "NM_005562.3",
"gene_symbol": "LAMC2",
"hgnc_id": 6493,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.2198G>C",
"hgvs_p": "p.Ser733Thr"
}
],
"clinvar_disease": " non-Herlitz type,Junctional epidermolysis bullosa,Junctional epidermolysis bullosa gravis of Herlitz,not provided,not specified",
"clinvar_classification": "Benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "B:7",
"phenotype_combined": "not specified|Junctional epidermolysis bullosa|not provided|Junctional epidermolysis bullosa gravis of Herlitz|Junctional epidermolysis bullosa, non-Herlitz type",
"pathogenicity_classification_combined": "Benign",
"custom_annotations": null
}
],
"message": null
}