← Back to variant description
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: 2-84573481-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=84573481&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 84573481,
"ref": "C",
"alt": "T",
"effect": "synonymous_variant",
"transcript": "ENST00000389394.8",
"consequences": [
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 77,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNAH6",
"gene_hgnc_id": 2951,
"hgvs_c": "c.1818C>T",
"hgvs_p": "p.Ala606Ala",
"transcript": "NM_001370.2",
"protein_id": "NP_001361.1",
"transcript_support_level": null,
"aa_start": 606,
"aa_end": null,
"aa_length": 4158,
"cds_start": 1818,
"cds_end": null,
"cds_length": 12477,
"cdna_start": 1912,
"cdna_end": null,
"cdna_length": 12752,
"mane_select": "ENST00000389394.8",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 77,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNAH6",
"gene_hgnc_id": 2951,
"hgvs_c": "c.1818C>T",
"hgvs_p": "p.Ala606Ala",
"transcript": "ENST00000389394.8",
"protein_id": "ENSP00000374045.3",
"transcript_support_level": 5,
"aa_start": 606,
"aa_end": null,
"aa_length": 4158,
"cds_start": 1818,
"cds_end": null,
"cds_length": 12477,
"cdna_start": 1912,
"cdna_end": null,
"cdna_length": 12752,
"mane_select": "NM_001370.2",
"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": 6,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNAH6",
"gene_hgnc_id": 2951,
"hgvs_c": "n.861C>T",
"hgvs_p": null,
"transcript": "ENST00000494025.1",
"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": 2065,
"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": 66,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNAH6",
"gene_hgnc_id": 2951,
"hgvs_c": "c.-23C>T",
"hgvs_p": null,
"transcript": "XM_047443590.1",
"protein_id": "XP_047299546.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 3494,
"cds_start": -4,
"cds_end": null,
"cds_length": 10485,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 10792,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 77,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNAH6",
"gene_hgnc_id": 2951,
"hgvs_c": "c.1818C>T",
"hgvs_p": "p.Ala606Ala",
"transcript": "XM_006711956.3",
"protein_id": "XP_006712019.1",
"transcript_support_level": null,
"aa_start": 606,
"aa_end": null,
"aa_length": 4158,
"cds_start": 1818,
"cds_end": null,
"cds_length": 12477,
"cdna_start": 2153,
"cdna_end": null,
"cdna_length": 12993,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 77,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNAH6",
"gene_hgnc_id": 2951,
"hgvs_c": "c.1818C>T",
"hgvs_p": "p.Ala606Ala",
"transcript": "XM_011532649.3",
"protein_id": "XP_011530951.1",
"transcript_support_level": null,
"aa_start": 606,
"aa_end": null,
"aa_length": 4158,
"cds_start": 1818,
"cds_end": null,
"cds_length": 12477,
"cdna_start": 1925,
"cdna_end": null,
"cdna_length": 12765,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 77,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNAH6",
"gene_hgnc_id": 2951,
"hgvs_c": "c.1818C>T",
"hgvs_p": "p.Ala606Ala",
"transcript": "XM_011532650.4",
"protein_id": "XP_011530952.1",
"transcript_support_level": null,
"aa_start": 606,
"aa_end": null,
"aa_length": 4158,
"cds_start": 1818,
"cds_end": null,
"cds_length": 12477,
"cdna_start": 1930,
"cdna_end": null,
"cdna_length": 12770,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 76,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNAH6",
"gene_hgnc_id": 2951,
"hgvs_c": "c.1818C>T",
"hgvs_p": "p.Ala606Ala",
"transcript": "XM_011532652.2",
"protein_id": "XP_011530954.1",
"transcript_support_level": null,
"aa_start": 606,
"aa_end": null,
"aa_length": 4116,
"cds_start": 1818,
"cds_end": null,
"cds_length": 12351,
"cdna_start": 1912,
"cdna_end": null,
"cdna_length": 12626,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 76,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNAH6",
"gene_hgnc_id": 2951,
"hgvs_c": "c.1818C>T",
"hgvs_p": "p.Ala606Ala",
"transcript": "XM_011532653.2",
"protein_id": "XP_011530955.1",
"transcript_support_level": null,
"aa_start": 606,
"aa_end": null,
"aa_length": 4109,
"cds_start": 1818,
"cds_end": null,
"cds_length": 12330,
"cdna_start": 1912,
"cdna_end": null,
"cdna_length": 12605,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 75,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNAH6",
"gene_hgnc_id": 2951,
"hgvs_c": "c.1818C>T",
"hgvs_p": "p.Ala606Ala",
"transcript": "XM_017003521.2",
"protein_id": "XP_016859010.1",
"transcript_support_level": null,
"aa_start": 606,
"aa_end": null,
"aa_length": 4067,
"cds_start": 1818,
"cds_end": null,
"cds_length": 12204,
"cdna_start": 1912,
"cdna_end": null,
"cdna_length": 12479,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 76,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNAH6",
"gene_hgnc_id": 2951,
"hgvs_c": "c.1428C>T",
"hgvs_p": "p.Ala476Ala",
"transcript": "XM_011532654.1",
"protein_id": "XP_011530956.1",
"transcript_support_level": null,
"aa_start": 476,
"aa_end": null,
"aa_length": 4028,
"cds_start": 1428,
"cds_end": null,
"cds_length": 12087,
"cdna_start": 1688,
"cdna_end": null,
"cdna_length": 12528,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 73,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNAH6",
"gene_hgnc_id": 2951,
"hgvs_c": "c.834C>T",
"hgvs_p": "p.Ala278Ala",
"transcript": "XM_011532655.2",
"protein_id": "XP_011530957.1",
"transcript_support_level": null,
"aa_start": 278,
"aa_end": null,
"aa_length": 3830,
"cds_start": 834,
"cds_end": null,
"cds_length": 11493,
"cdna_start": 977,
"cdna_end": null,
"cdna_length": 11817,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 71,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNAH6",
"gene_hgnc_id": 2951,
"hgvs_c": "c.555C>T",
"hgvs_p": "p.Ala185Ala",
"transcript": "XM_011532657.1",
"protein_id": "XP_011530959.1",
"transcript_support_level": null,
"aa_start": 185,
"aa_end": null,
"aa_length": 3737,
"cds_start": 555,
"cds_end": null,
"cds_length": 11214,
"cdna_start": 716,
"cdna_end": null,
"cdna_length": 11556,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 71,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNAH6",
"gene_hgnc_id": 2951,
"hgvs_c": "c.555C>T",
"hgvs_p": "p.Ala185Ala",
"transcript": "XM_047443589.1",
"protein_id": "XP_047299545.1",
"transcript_support_level": null,
"aa_start": 185,
"aa_end": null,
"aa_length": 3737,
"cds_start": 555,
"cds_end": null,
"cds_length": 11214,
"cdna_start": 707,
"cdna_end": null,
"cdna_length": 11547,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 43,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNAH6",
"gene_hgnc_id": 2951,
"hgvs_c": "c.1818C>T",
"hgvs_p": "p.Ala606Ala",
"transcript": "XM_011532660.2",
"protein_id": "XP_011530962.1",
"transcript_support_level": null,
"aa_start": 606,
"aa_end": null,
"aa_length": 2275,
"cds_start": 1818,
"cds_end": null,
"cds_length": 6828,
"cdna_start": 1912,
"cdna_end": null,
"cdna_length": 7030,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 41,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNAH6",
"gene_hgnc_id": 2951,
"hgvs_c": "c.1818C>T",
"hgvs_p": "p.Ala606Ala",
"transcript": "XM_017003524.2",
"protein_id": "XP_016859013.1",
"transcript_support_level": null,
"aa_start": 606,
"aa_end": null,
"aa_length": 2213,
"cds_start": 1818,
"cds_end": null,
"cds_length": 6642,
"cdna_start": 1912,
"cdna_end": null,
"cdna_length": 6832,
"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": 8,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNAH6",
"gene_hgnc_id": 2951,
"hgvs_c": "n.1168C>T",
"hgvs_p": null,
"transcript": "ENST00000476689.5",
"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,
"cdna_end": null,
"cdna_length": 2435,
"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": 66,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "DNAH6",
"gene_hgnc_id": 2951,
"hgvs_c": "c.-23C>T",
"hgvs_p": null,
"transcript": "XM_047443590.1",
"protein_id": "XP_047299546.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 3494,
"cds_start": -4,
"cds_end": null,
"cds_length": 10485,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 10792,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "DNAH6",
"gene_hgnc_id": 2951,
"dbsnp": "rs11891970",
"frequency_reference_population": 0.0000014021175,
"hom_count_reference_population": 0,
"allele_count_reference_population": 2,
"gnomad_exomes_af": 0.00000140212,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 2,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.4000000059604645,
"computational_prediction_selected": "Benign",
"computational_source_selected": "BayesDel_noAF",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.4,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.364,
"phylop100way_prediction": "Benign",
"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": -1,
"acmg_classification": "Likely_benign",
"acmg_criteria": "PM2,BP4_Moderate,BP7",
"acmg_by_gene": [
{
"score": -1,
"benign_score": 3,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Moderate",
"BP7"
],
"verdict": "Likely_benign",
"transcript": "ENST00000389394.8",
"gene_symbol": "DNAH6",
"hgnc_id": 2951,
"effects": [
"synonymous_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.1818C>T",
"hgvs_p": "p.Ala606Ala"
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}