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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: 2-96253862-C-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=96253862&ref=C&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 96253862,
"ref": "C",
"alt": "G",
"effect": "synonymous_variant",
"transcript": "NM_017849.4",
"consequences": [
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TMEM127",
"gene_hgnc_id": 26038,
"hgvs_c": "c.663G>C",
"hgvs_p": "p.Pro221Pro",
"transcript": "NM_017849.4",
"protein_id": "NP_060319.1",
"transcript_support_level": null,
"aa_start": 221,
"aa_end": null,
"aa_length": 238,
"cds_start": 663,
"cds_end": null,
"cds_length": 717,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000258439.8",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_017849.4"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TMEM127",
"gene_hgnc_id": 26038,
"hgvs_c": "c.663G>C",
"hgvs_p": "p.Pro221Pro",
"transcript": "ENST00000258439.8",
"protein_id": "ENSP00000258439.3",
"transcript_support_level": 1,
"aa_start": 221,
"aa_end": null,
"aa_length": 238,
"cds_start": 663,
"cds_end": null,
"cds_length": 717,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_017849.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000258439.8"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TMEM127",
"gene_hgnc_id": 26038,
"hgvs_c": "c.663G>C",
"hgvs_p": "p.Pro221Pro",
"transcript": "ENST00000432959.2",
"protein_id": "ENSP00000416660.1",
"transcript_support_level": 1,
"aa_start": 221,
"aa_end": null,
"aa_length": 238,
"cds_start": 663,
"cds_end": null,
"cds_length": 717,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000432959.2"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TMEM127",
"gene_hgnc_id": 26038,
"hgvs_c": "c.663G>C",
"hgvs_p": "p.Pro221Pro",
"transcript": "NM_001193304.3",
"protein_id": "NP_001180233.1",
"transcript_support_level": null,
"aa_start": 221,
"aa_end": null,
"aa_length": 238,
"cds_start": 663,
"cds_end": null,
"cds_length": 717,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001193304.3"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TMEM127",
"gene_hgnc_id": 26038,
"hgvs_c": "c.663G>C",
"hgvs_p": "p.Pro221Pro",
"transcript": "ENST00000910913.1",
"protein_id": "ENSP00000580972.1",
"transcript_support_level": null,
"aa_start": 221,
"aa_end": null,
"aa_length": 238,
"cds_start": 663,
"cds_end": null,
"cds_length": 717,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000910913.1"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TMEM127",
"gene_hgnc_id": 26038,
"hgvs_c": "c.663G>C",
"hgvs_p": "p.Pro221Pro",
"transcript": "ENST00000910914.1",
"protein_id": "ENSP00000580973.1",
"transcript_support_level": null,
"aa_start": 221,
"aa_end": null,
"aa_length": 238,
"cds_start": 663,
"cds_end": null,
"cds_length": 717,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000910914.1"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TMEM127",
"gene_hgnc_id": 26038,
"hgvs_c": "c.663G>C",
"hgvs_p": "p.Pro221Pro",
"transcript": "ENST00000910915.1",
"protein_id": "ENSP00000580974.1",
"transcript_support_level": null,
"aa_start": 221,
"aa_end": null,
"aa_length": 238,
"cds_start": 663,
"cds_end": null,
"cds_length": 717,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000910915.1"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TMEM127",
"gene_hgnc_id": 26038,
"hgvs_c": "c.663G>C",
"hgvs_p": "p.Pro221Pro",
"transcript": "ENST00000939309.1",
"protein_id": "ENSP00000609368.1",
"transcript_support_level": null,
"aa_start": 221,
"aa_end": null,
"aa_length": 238,
"cds_start": 663,
"cds_end": null,
"cds_length": 717,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000939309.1"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TMEM127",
"gene_hgnc_id": 26038,
"hgvs_c": "c.663G>C",
"hgvs_p": "p.Pro221Pro",
"transcript": "ENST00000963839.1",
"protein_id": "ENSP00000633898.1",
"transcript_support_level": null,
"aa_start": 221,
"aa_end": null,
"aa_length": 238,
"cds_start": 663,
"cds_end": null,
"cds_length": 717,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000963839.1"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TMEM127",
"gene_hgnc_id": 26038,
"hgvs_c": "c.639G>C",
"hgvs_p": "p.Pro213Pro",
"transcript": "ENST00000939308.1",
"protein_id": "ENSP00000609367.1",
"transcript_support_level": null,
"aa_start": 213,
"aa_end": null,
"aa_length": 230,
"cds_start": 639,
"cds_end": null,
"cds_length": 693,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000939308.1"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TMEM127",
"gene_hgnc_id": 26038,
"hgvs_c": "c.639G>C",
"hgvs_p": "p.Pro213Pro",
"transcript": "ENST00000963838.1",
"protein_id": "ENSP00000633897.1",
"transcript_support_level": null,
"aa_start": 213,
"aa_end": null,
"aa_length": 230,
"cds_start": 639,
"cds_end": null,
"cds_length": 693,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000963838.1"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TMEM127",
"gene_hgnc_id": 26038,
"hgvs_c": "c.411G>C",
"hgvs_p": "p.Pro137Pro",
"transcript": "NM_001407282.1",
"protein_id": "NP_001394211.1",
"transcript_support_level": null,
"aa_start": 137,
"aa_end": null,
"aa_length": 154,
"cds_start": 411,
"cds_end": null,
"cds_length": 465,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001407282.1"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TMEM127",
"gene_hgnc_id": 26038,
"hgvs_c": "c.411G>C",
"hgvs_p": "p.Pro137Pro",
"transcript": "NM_001407283.1",
"protein_id": "NP_001394212.1",
"transcript_support_level": null,
"aa_start": 137,
"aa_end": null,
"aa_length": 154,
"cds_start": 411,
"cds_end": null,
"cds_length": 465,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001407283.1"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TMEM127",
"gene_hgnc_id": 26038,
"hgvs_c": "c.411G>C",
"hgvs_p": "p.Pro137Pro",
"transcript": "ENST00000435268.2",
"protein_id": "ENSP00000411810.1",
"transcript_support_level": 3,
"aa_start": 137,
"aa_end": null,
"aa_length": 154,
"cds_start": 411,
"cds_end": null,
"cds_length": 465,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000435268.2"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TMEM127",
"gene_hgnc_id": 26038,
"hgvs_c": "c.411G>C",
"hgvs_p": "p.Pro137Pro",
"transcript": "ENST00000713752.1",
"protein_id": "ENSP00000519053.1",
"transcript_support_level": null,
"aa_start": 137,
"aa_end": null,
"aa_length": 154,
"cds_start": 411,
"cds_end": null,
"cds_length": 465,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000713752.1"
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TMEM127",
"gene_hgnc_id": 26038,
"hgvs_c": "c.411G>C",
"hgvs_p": "p.Pro137Pro",
"transcript": "ENST00000713753.1",
"protein_id": "ENSP00000519054.1",
"transcript_support_level": null,
"aa_start": 137,
"aa_end": null,
"aa_length": 154,
"cds_start": 411,
"cds_end": null,
"cds_length": 465,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000713753.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TMEM127",
"gene_hgnc_id": 26038,
"hgvs_c": "n.*343G>C",
"hgvs_p": null,
"transcript": "ENST00000713754.1",
"protein_id": "ENSP00000519055.1",
"transcript_support_level": null,
"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": "ENST00000713754.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TMEM127",
"gene_hgnc_id": 26038,
"hgvs_c": "n.*407G>C",
"hgvs_p": null,
"transcript": "ENST00000713755.1",
"protein_id": "ENSP00000519056.1",
"transcript_support_level": null,
"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": "ENST00000713755.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TMEM127",
"gene_hgnc_id": 26038,
"hgvs_c": "n.*431G>C",
"hgvs_p": null,
"transcript": "ENST00000713756.1",
"protein_id": "ENSP00000519057.1",
"transcript_support_level": null,
"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": "ENST00000713756.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TMEM127",
"gene_hgnc_id": 26038,
"hgvs_c": "n.*343G>C",
"hgvs_p": null,
"transcript": "ENST00000713754.1",
"protein_id": "ENSP00000519055.1",
"transcript_support_level": null,
"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": "ENST00000713754.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TMEM127",
"gene_hgnc_id": 26038,
"hgvs_c": "n.*407G>C",
"hgvs_p": null,
"transcript": "ENST00000713755.1",
"protein_id": "ENSP00000519056.1",
"transcript_support_level": null,
"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": "ENST00000713755.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TMEM127",
"gene_hgnc_id": 26038,
"hgvs_c": "n.*431G>C",
"hgvs_p": null,
"transcript": "ENST00000713756.1",
"protein_id": "ENSP00000519057.1",
"transcript_support_level": null,
"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": "ENST00000713756.1"
}
],
"gene_symbol": "TMEM127",
"gene_hgnc_id": 26038,
"dbsnp": "rs377760956",
"frequency_reference_population": null,
"hom_count_reference_population": 0,
"allele_count_reference_population": 0,
"gnomad_exomes_af": null,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": null,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": null,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.7900000214576721,
"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": -0.79,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -3.475,
"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": -3,
"acmg_classification": "Likely_benign",
"acmg_criteria": "PM2,BP4_Strong,BP7",
"acmg_by_gene": [
{
"score": -3,
"benign_score": 5,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Strong",
"BP7"
],
"verdict": "Likely_benign",
"transcript": "NM_017849.4",
"gene_symbol": "TMEM127",
"hgnc_id": 26038,
"effects": [
"synonymous_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.663G>C",
"hgvs_p": "p.Pro221Pro"
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}