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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: 2-227695929-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=227695929&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 227695929,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_025243.4",
"consequences": [
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC19A3",
"gene_hgnc_id": 16266,
"hgvs_c": "c.1132A>G",
"hgvs_p": "p.Ile378Val",
"transcript": "NM_025243.4",
"protein_id": "NP_079519.1",
"transcript_support_level": null,
"aa_start": 378,
"aa_end": null,
"aa_length": 496,
"cds_start": 1132,
"cds_end": null,
"cds_length": 1491,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000644224.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_025243.4"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC19A3",
"gene_hgnc_id": 16266,
"hgvs_c": "c.1132A>G",
"hgvs_p": "p.Ile378Val",
"transcript": "ENST00000644224.2",
"protein_id": "ENSP00000495385.1",
"transcript_support_level": null,
"aa_start": 378,
"aa_end": null,
"aa_length": 496,
"cds_start": 1132,
"cds_end": null,
"cds_length": 1491,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_025243.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000644224.2"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC19A3",
"gene_hgnc_id": 16266,
"hgvs_c": "c.1132A>G",
"hgvs_p": "p.Ile378Val",
"transcript": "ENST00000258403.8",
"protein_id": "ENSP00000258403.3",
"transcript_support_level": 1,
"aa_start": 378,
"aa_end": null,
"aa_length": 496,
"cds_start": 1132,
"cds_end": null,
"cds_length": 1491,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000258403.8"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC19A3",
"gene_hgnc_id": 16266,
"hgvs_c": "n.*1157A>G",
"hgvs_p": null,
"transcript": "ENST00000425817.6",
"protein_id": "ENSP00000397393.2",
"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": "ENST00000425817.6"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC19A3",
"gene_hgnc_id": 16266,
"hgvs_c": "n.*1157A>G",
"hgvs_p": null,
"transcript": "ENST00000425817.6",
"protein_id": "ENSP00000397393.2",
"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": "ENST00000425817.6"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC19A3",
"gene_hgnc_id": 16266,
"hgvs_c": "c.1336A>G",
"hgvs_p": "p.Ile446Val",
"transcript": "ENST00000855519.1",
"protein_id": "ENSP00000525578.1",
"transcript_support_level": null,
"aa_start": 446,
"aa_end": null,
"aa_length": 564,
"cds_start": 1336,
"cds_end": null,
"cds_length": 1695,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000855519.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC19A3",
"gene_hgnc_id": 16266,
"hgvs_c": "c.1168A>G",
"hgvs_p": "p.Ile390Val",
"transcript": "ENST00000646591.1",
"protein_id": "ENSP00000496701.1",
"transcript_support_level": null,
"aa_start": 390,
"aa_end": null,
"aa_length": 508,
"cds_start": 1168,
"cds_end": null,
"cds_length": 1527,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000646591.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC19A3",
"gene_hgnc_id": 16266,
"hgvs_c": "c.1132A>G",
"hgvs_p": "p.Ile378Val",
"transcript": "NM_001371411.1",
"protein_id": "NP_001358340.1",
"transcript_support_level": null,
"aa_start": 378,
"aa_end": null,
"aa_length": 496,
"cds_start": 1132,
"cds_end": null,
"cds_length": 1491,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001371411.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC19A3",
"gene_hgnc_id": 16266,
"hgvs_c": "c.1132A>G",
"hgvs_p": "p.Ile378Val",
"transcript": "NM_001371412.1",
"protein_id": "NP_001358341.1",
"transcript_support_level": null,
"aa_start": 378,
"aa_end": null,
"aa_length": 496,
"cds_start": 1132,
"cds_end": null,
"cds_length": 1491,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001371412.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC19A3",
"gene_hgnc_id": 16266,
"hgvs_c": "c.1132A>G",
"hgvs_p": "p.Ile378Val",
"transcript": "ENST00000855517.1",
"protein_id": "ENSP00000525576.1",
"transcript_support_level": null,
"aa_start": 378,
"aa_end": null,
"aa_length": 496,
"cds_start": 1132,
"cds_end": null,
"cds_length": 1491,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000855517.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC19A3",
"gene_hgnc_id": 16266,
"hgvs_c": "c.1132A>G",
"hgvs_p": "p.Ile378Val",
"transcript": "ENST00000855518.1",
"protein_id": "ENSP00000525577.1",
"transcript_support_level": null,
"aa_start": 378,
"aa_end": null,
"aa_length": 496,
"cds_start": 1132,
"cds_end": null,
"cds_length": 1491,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000855518.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC19A3",
"gene_hgnc_id": 16266,
"hgvs_c": "c.1132A>G",
"hgvs_p": "p.Ile378Val",
"transcript": "ENST00000958931.1",
"protein_id": "ENSP00000628990.1",
"transcript_support_level": null,
"aa_start": 378,
"aa_end": null,
"aa_length": 496,
"cds_start": 1132,
"cds_end": null,
"cds_length": 1491,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000958931.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC19A3",
"gene_hgnc_id": 16266,
"hgvs_c": "c.1132A>G",
"hgvs_p": "p.Ile378Val",
"transcript": "ENST00000958932.1",
"protein_id": "ENSP00000628991.1",
"transcript_support_level": null,
"aa_start": 378,
"aa_end": null,
"aa_length": 496,
"cds_start": 1132,
"cds_end": null,
"cds_length": 1491,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000958932.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC19A3",
"gene_hgnc_id": 16266,
"hgvs_c": "c.1132A>G",
"hgvs_p": "p.Ile378Val",
"transcript": "ENST00000958933.1",
"protein_id": "ENSP00000628992.1",
"transcript_support_level": null,
"aa_start": 378,
"aa_end": null,
"aa_length": 496,
"cds_start": 1132,
"cds_end": null,
"cds_length": 1491,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000958933.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC19A3",
"gene_hgnc_id": 16266,
"hgvs_c": "c.1132A>G",
"hgvs_p": "p.Ile378Val",
"transcript": "ENST00000958934.1",
"protein_id": "ENSP00000628993.1",
"transcript_support_level": null,
"aa_start": 378,
"aa_end": null,
"aa_length": 496,
"cds_start": 1132,
"cds_end": null,
"cds_length": 1491,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000958934.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC19A3",
"gene_hgnc_id": 16266,
"hgvs_c": "c.1132A>G",
"hgvs_p": "p.Ile378Val",
"transcript": "ENST00000958936.1",
"protein_id": "ENSP00000628995.1",
"transcript_support_level": null,
"aa_start": 378,
"aa_end": null,
"aa_length": 496,
"cds_start": 1132,
"cds_end": null,
"cds_length": 1491,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000958936.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC19A3",
"gene_hgnc_id": 16266,
"hgvs_c": "c.1132A>G",
"hgvs_p": "p.Ile378Val",
"transcript": "ENST00000958937.1",
"protein_id": "ENSP00000628996.1",
"transcript_support_level": null,
"aa_start": 378,
"aa_end": null,
"aa_length": 496,
"cds_start": 1132,
"cds_end": null,
"cds_length": 1491,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000958937.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC19A3",
"gene_hgnc_id": 16266,
"hgvs_c": "c.1132A>G",
"hgvs_p": "p.Ile378Val",
"transcript": "ENST00000958938.1",
"protein_id": "ENSP00000628997.1",
"transcript_support_level": null,
"aa_start": 378,
"aa_end": null,
"aa_length": 496,
"cds_start": 1132,
"cds_end": null,
"cds_length": 1491,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000958938.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC19A3",
"gene_hgnc_id": 16266,
"hgvs_c": "c.1120A>G",
"hgvs_p": "p.Ile374Val",
"transcript": "NM_001371413.1",
"protein_id": "NP_001358342.1",
"transcript_support_level": null,
"aa_start": 374,
"aa_end": null,
"aa_length": 492,
"cds_start": 1120,
"cds_end": null,
"cds_length": 1479,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001371413.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC19A3",
"gene_hgnc_id": 16266,
"hgvs_c": "c.1120A>G",
"hgvs_p": "p.Ile374Val",
"transcript": "NM_001371414.1",
"protein_id": "NP_001358343.1",
"transcript_support_level": null,
"aa_start": 374,
"aa_end": null,
"aa_length": 492,
"cds_start": 1120,
"cds_end": null,
"cds_length": 1479,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001371414.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC19A3",
"gene_hgnc_id": 16266,
"hgvs_c": "c.412A>G",
"hgvs_p": "p.Ile138Val",
"transcript": "ENST00000958935.1",
"protein_id": "ENSP00000628994.1",
"transcript_support_level": null,
"aa_start": 138,
"aa_end": null,
"aa_length": 256,
"cds_start": 412,
"cds_end": null,
"cds_length": 771,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000958935.1"
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC19A3",
"gene_hgnc_id": 16266,
"hgvs_c": "c.1168A>G",
"hgvs_p": "p.Ile390Val",
"transcript": "XM_047445927.1",
"protein_id": "XP_047301883.1",
"transcript_support_level": null,
"aa_start": 390,
"aa_end": null,
"aa_length": 508,
"cds_start": 1168,
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],
"gene_symbol": "SLC19A3",
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"dbsnp": "rs117864472",
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"hom_count_reference_population": 18,
"allele_count_reference_population": 1203,
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"computational_score_selected": 0.008207350969314575,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.05000000074505806,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.15,
"revel_prediction": "Benign",
"alphamissense_score": 0.0691,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.48,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -0.949,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0.05,
"spliceai_max_prediction": "Benign",
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"mitotip_score": null,
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"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": [
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"BP6_Very_Strong",
"BS1",
"BS2"
],
"verdict": "Benign",
"transcript": "NM_025243.4",
"gene_symbol": "SLC19A3",
"hgnc_id": 16266,
"effects": [
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],
"inheritance_mode": "AR",
"hgvs_c": "c.1132A>G",
"hgvs_p": "p.Ile378Val"
}
],
"clinvar_disease": "Biotin-responsive basal ganglia disease,SLC19A3-related disorder,not provided",
"clinvar_classification": "Benign/Likely benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "LB:3 B:2",
"phenotype_combined": "not provided|Biotin-responsive basal ganglia disease|SLC19A3-related disorder",
"pathogenicity_classification_combined": "Benign/Likely benign",
"custom_annotations": null
}
],
"message": null
}