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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: 2-38995183-A-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=38995183&ref=A&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 38995183,
"ref": "A",
"alt": "T",
"effect": "missense_variant",
"transcript": "ENST00000402219.8",
"consequences": [
{
"aa_ref": "S",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "c.3286T>A",
"hgvs_p": "p.Ser1096Thr",
"transcript": "NM_005633.4",
"protein_id": "NP_005624.2",
"transcript_support_level": null,
"aa_start": 1096,
"aa_end": null,
"aa_length": 1333,
"cds_start": 3286,
"cds_end": null,
"cds_length": 4002,
"cdna_start": 3915,
"cdna_end": null,
"cdna_length": 8906,
"mane_select": "ENST00000402219.8",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "T",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "c.3286T>A",
"hgvs_p": "p.Ser1096Thr",
"transcript": "ENST00000402219.8",
"protein_id": "ENSP00000384675.2",
"transcript_support_level": 1,
"aa_start": 1096,
"aa_end": null,
"aa_length": 1333,
"cds_start": 3286,
"cds_end": null,
"cds_length": 4002,
"cdna_start": 3915,
"cdna_end": null,
"cdna_length": 8906,
"mane_select": "NM_005633.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "c.3265T>A",
"hgvs_p": "p.Ser1089Thr",
"transcript": "NM_001382394.1",
"protein_id": "NP_001369323.1",
"transcript_support_level": null,
"aa_start": 1089,
"aa_end": null,
"aa_length": 1326,
"cds_start": 3265,
"cds_end": null,
"cds_length": 3981,
"cdna_start": 3404,
"cdna_end": null,
"cdna_length": 8395,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "c.3286T>A",
"hgvs_p": "p.Ser1096Thr",
"transcript": "NM_001382395.1",
"protein_id": "NP_001369324.1",
"transcript_support_level": null,
"aa_start": 1096,
"aa_end": null,
"aa_length": 1318,
"cds_start": 3286,
"cds_end": null,
"cds_length": 3957,
"cdna_start": 3915,
"cdna_end": null,
"cdna_length": 8861,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "c.3286T>A",
"hgvs_p": "p.Ser1096Thr",
"transcript": "ENST00000395038.6",
"protein_id": "ENSP00000378479.2",
"transcript_support_level": 5,
"aa_start": 1096,
"aa_end": null,
"aa_length": 1318,
"cds_start": 3286,
"cds_end": null,
"cds_length": 3957,
"cdna_start": 3314,
"cdna_end": null,
"cdna_length": 4123,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "c.3175T>A",
"hgvs_p": "p.Ser1059Thr",
"transcript": "ENST00000692089.1",
"protein_id": "ENSP00000508626.1",
"transcript_support_level": null,
"aa_start": 1059,
"aa_end": null,
"aa_length": 1147,
"cds_start": 3175,
"cds_end": null,
"cds_length": 3444,
"cdna_start": 3192,
"cdna_end": null,
"cdna_length": 4056,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "c.3055T>A",
"hgvs_p": "p.Ser1019Thr",
"transcript": "ENST00000691229.1",
"protein_id": "ENSP00000510437.1",
"transcript_support_level": null,
"aa_start": 1019,
"aa_end": null,
"aa_length": 1086,
"cds_start": 3055,
"cds_end": null,
"cds_length": 3261,
"cdna_start": 3072,
"cdna_end": null,
"cdna_length": 5976,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "c.2053T>A",
"hgvs_p": "p.Ser685Thr",
"transcript": "ENST00000685279.1",
"protein_id": "ENSP00000509424.1",
"transcript_support_level": null,
"aa_start": 685,
"aa_end": null,
"aa_length": 922,
"cds_start": 2053,
"cds_end": null,
"cds_length": 2769,
"cdna_start": 2120,
"cdna_end": null,
"cdna_length": 7030,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "c.982T>A",
"hgvs_p": "p.Ser328Thr",
"transcript": "ENST00000692227.1",
"protein_id": "ENSP00000509138.1",
"transcript_support_level": null,
"aa_start": 328,
"aa_end": null,
"aa_length": 404,
"cds_start": 982,
"cds_end": null,
"cds_length": 1215,
"cdna_start": 982,
"cdna_end": null,
"cdna_length": 1735,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "c.3265T>A",
"hgvs_p": "p.Ser1089Thr",
"transcript": "XM_047445581.1",
"protein_id": "XP_047301537.1",
"transcript_support_level": null,
"aa_start": 1089,
"aa_end": null,
"aa_length": 1311,
"cds_start": 3265,
"cds_end": null,
"cds_length": 3936,
"cdna_start": 3404,
"cdna_end": null,
"cdna_length": 8350,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "c.3115T>A",
"hgvs_p": "p.Ser1039Thr",
"transcript": "XM_011533064.3",
"protein_id": "XP_011531366.1",
"transcript_support_level": null,
"aa_start": 1039,
"aa_end": null,
"aa_length": 1276,
"cds_start": 3115,
"cds_end": null,
"cds_length": 3831,
"cdna_start": 6875,
"cdna_end": null,
"cdna_length": 11866,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "c.3115T>A",
"hgvs_p": "p.Ser1039Thr",
"transcript": "XM_047445582.1",
"protein_id": "XP_047301538.1",
"transcript_support_level": null,
"aa_start": 1039,
"aa_end": null,
"aa_length": 1276,
"cds_start": 3115,
"cds_end": null,
"cds_length": 3831,
"cdna_start": 3505,
"cdna_end": null,
"cdna_length": 8496,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "c.3286T>A",
"hgvs_p": "p.Ser1096Thr",
"transcript": "XM_047445583.1",
"protein_id": "XP_047301539.1",
"transcript_support_level": null,
"aa_start": 1096,
"aa_end": null,
"aa_length": 1187,
"cds_start": 3286,
"cds_end": null,
"cds_length": 3564,
"cdna_start": 3915,
"cdna_end": null,
"cdna_length": 7951,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "c.3286T>A",
"hgvs_p": "p.Ser1096Thr",
"transcript": "XM_047445584.1",
"protein_id": "XP_047301540.1",
"transcript_support_level": null,
"aa_start": 1096,
"aa_end": null,
"aa_length": 1172,
"cds_start": 3286,
"cds_end": null,
"cds_length": 3519,
"cdna_start": 3915,
"cdna_end": null,
"cdna_length": 7906,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "c.2221T>A",
"hgvs_p": "p.Ser741Thr",
"transcript": "XM_047445585.1",
"protein_id": "XP_047301541.1",
"transcript_support_level": null,
"aa_start": 741,
"aa_end": null,
"aa_length": 978,
"cds_start": 2221,
"cds_end": null,
"cds_length": 2937,
"cdna_start": 2236,
"cdna_end": null,
"cdna_length": 7227,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "T",
"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": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "c.1147T>A",
"hgvs_p": "p.Ser383Thr",
"transcript": "XM_047445586.1",
"protein_id": "XP_047301542.1",
"transcript_support_level": null,
"aa_start": 383,
"aa_end": null,
"aa_length": 620,
"cds_start": 1147,
"cds_end": null,
"cds_length": 1863,
"cdna_start": 1430,
"cdna_end": null,
"cdna_length": 6421,
"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": 20,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "n.*592T>A",
"hgvs_p": null,
"transcript": "ENST00000690876.1",
"protein_id": "ENSP00000508955.1",
"transcript_support_level": null,
"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": 5987,
"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": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "n.*873T>A",
"hgvs_p": null,
"transcript": "ENST00000692620.1",
"protein_id": "ENSP00000509311.1",
"transcript_support_level": null,
"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": 4772,
"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": 20,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "n.*592T>A",
"hgvs_p": null,
"transcript": "ENST00000690876.1",
"protein_id": "ENSP00000508955.1",
"transcript_support_level": null,
"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": 5987,
"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": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"hgvs_c": "n.*873T>A",
"hgvs_p": null,
"transcript": "ENST00000692620.1",
"protein_id": "ENSP00000509311.1",
"transcript_support_level": null,
"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": 4772,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "SOS1",
"gene_hgnc_id": 11187,
"dbsnp": "rs376722127",
"frequency_reference_population": 0.00036437277,
"hom_count_reference_population": 0,
"allele_count_reference_population": 588,
"gnomad_exomes_af": 0.000385217,
"gnomad_genomes_af": 0.000164238,
"gnomad_exomes_ac": 563,
"gnomad_genomes_ac": 25,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.25004833936691284,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.333,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.0969,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.17,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 6.563,
"phylop100way_prediction": "Uncertain_significance",
"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": 0,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "",
"acmg_by_gene": [
{
"score": 0,
"benign_score": 0,
"pathogenic_score": 0,
"criteria": [],
"verdict": "Uncertain_significance",
"transcript": "ENST00000402219.8",
"gene_symbol": "SOS1",
"hgnc_id": 11187,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.3286T>A",
"hgvs_p": "p.Ser1096Thr"
}
],
"clinvar_disease": " 1, gingival,Cardiovascular phenotype,Fibromatosis,Noonan syndrome,Noonan syndrome 4,RASopathy,not provided,not specified",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "reviewed by expert panel",
"clinvar_submissions_summary": "US:4 LB:4 B:1",
"phenotype_combined": "RASopathy|not specified|Noonan syndrome|Noonan syndrome 4|Fibromatosis, gingival, 1|not provided|Cardiovascular phenotype|Noonan syndrome 4;Fibromatosis, gingival, 1",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}