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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: 9-130622807-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=9&pos=130622807&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "9",
"pos": 130622807,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_003934.2",
"consequences": [
{
"aa_ref": "P",
"aa_alt": "S",
"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": "FUBP3",
"gene_hgnc_id": 4005,
"hgvs_c": "c.871C>T",
"hgvs_p": "p.Pro291Ser",
"transcript": "NM_003934.2",
"protein_id": "NP_003925.1",
"transcript_support_level": null,
"aa_start": 291,
"aa_end": null,
"aa_length": 572,
"cds_start": 871,
"cds_end": null,
"cds_length": 1719,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000319725.10",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_003934.2"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": true,
"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": "FUBP3",
"gene_hgnc_id": 4005,
"hgvs_c": "c.871C>T",
"hgvs_p": "p.Pro291Ser",
"transcript": "ENST00000319725.10",
"protein_id": "ENSP00000318177.9",
"transcript_support_level": 1,
"aa_start": 291,
"aa_end": null,
"aa_length": 572,
"cds_start": 871,
"cds_end": null,
"cds_length": 1719,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_003934.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000319725.10"
},
{
"aa_ref": "P",
"aa_alt": "S",
"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": "FUBP3",
"gene_hgnc_id": 4005,
"hgvs_c": "c.964C>T",
"hgvs_p": "p.Pro322Ser",
"transcript": "ENST00000964145.1",
"protein_id": "ENSP00000634204.1",
"transcript_support_level": null,
"aa_start": 322,
"aa_end": null,
"aa_length": 603,
"cds_start": 964,
"cds_end": null,
"cds_length": 1812,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000964145.1"
},
{
"aa_ref": "P",
"aa_alt": "S",
"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": "FUBP3",
"gene_hgnc_id": 4005,
"hgvs_c": "c.913C>T",
"hgvs_p": "p.Pro305Ser",
"transcript": "ENST00000936135.1",
"protein_id": "ENSP00000606194.1",
"transcript_support_level": null,
"aa_start": 305,
"aa_end": null,
"aa_length": 586,
"cds_start": 913,
"cds_end": null,
"cds_length": 1761,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000936135.1"
},
{
"aa_ref": "P",
"aa_alt": "S",
"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": "FUBP3",
"gene_hgnc_id": 4005,
"hgvs_c": "c.871C>T",
"hgvs_p": "p.Pro291Ser",
"transcript": "ENST00000936137.1",
"protein_id": "ENSP00000606196.1",
"transcript_support_level": null,
"aa_start": 291,
"aa_end": null,
"aa_length": 581,
"cds_start": 871,
"cds_end": null,
"cds_length": 1746,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000936137.1"
},
{
"aa_ref": "P",
"aa_alt": "S",
"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": "FUBP3",
"gene_hgnc_id": 4005,
"hgvs_c": "c.868C>T",
"hgvs_p": "p.Pro290Ser",
"transcript": "ENST00000863495.1",
"protein_id": "ENSP00000533554.1",
"transcript_support_level": null,
"aa_start": 290,
"aa_end": null,
"aa_length": 571,
"cds_start": 868,
"cds_end": null,
"cds_length": 1716,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000863495.1"
},
{
"aa_ref": "P",
"aa_alt": "S",
"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": "FUBP3",
"gene_hgnc_id": 4005,
"hgvs_c": "c.871C>T",
"hgvs_p": "p.Pro291Ser",
"transcript": "ENST00000936136.1",
"protein_id": "ENSP00000606195.1",
"transcript_support_level": null,
"aa_start": 291,
"aa_end": null,
"aa_length": 561,
"cds_start": 871,
"cds_end": null,
"cds_length": 1686,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000936136.1"
},
{
"aa_ref": "P",
"aa_alt": "S",
"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": "FUBP3",
"gene_hgnc_id": 4005,
"hgvs_c": "c.814C>T",
"hgvs_p": "p.Pro272Ser",
"transcript": "ENST00000964142.1",
"protein_id": "ENSP00000634201.1",
"transcript_support_level": null,
"aa_start": 272,
"aa_end": null,
"aa_length": 553,
"cds_start": 814,
"cds_end": null,
"cds_length": 1662,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000964142.1"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FUBP3",
"gene_hgnc_id": 4005,
"hgvs_c": "c.811C>T",
"hgvs_p": "p.Pro271Ser",
"transcript": "ENST00000863499.1",
"protein_id": "ENSP00000533558.1",
"transcript_support_level": null,
"aa_start": 271,
"aa_end": null,
"aa_length": 552,
"cds_start": 811,
"cds_end": null,
"cds_length": 1659,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000863499.1"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FUBP3",
"gene_hgnc_id": 4005,
"hgvs_c": "c.871C>T",
"hgvs_p": "p.Pro291Ser",
"transcript": "ENST00000863494.1",
"protein_id": "ENSP00000533553.1",
"transcript_support_level": null,
"aa_start": 291,
"aa_end": null,
"aa_length": 548,
"cds_start": 871,
"cds_end": null,
"cds_length": 1647,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000863494.1"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FUBP3",
"gene_hgnc_id": 4005,
"hgvs_c": "c.868C>T",
"hgvs_p": "p.Pro290Ser",
"transcript": "ENST00000863497.1",
"protein_id": "ENSP00000533556.1",
"transcript_support_level": null,
"aa_start": 290,
"aa_end": null,
"aa_length": 547,
"cds_start": 868,
"cds_end": null,
"cds_length": 1644,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000863497.1"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FUBP3",
"gene_hgnc_id": 4005,
"hgvs_c": "c.871C>T",
"hgvs_p": "p.Pro291Ser",
"transcript": "ENST00000964144.1",
"protein_id": "ENSP00000634203.1",
"transcript_support_level": null,
"aa_start": 291,
"aa_end": null,
"aa_length": 547,
"cds_start": 871,
"cds_end": null,
"cds_length": 1644,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000964144.1"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FUBP3",
"gene_hgnc_id": 4005,
"hgvs_c": "c.871C>T",
"hgvs_p": "p.Pro291Ser",
"transcript": "ENST00000863496.1",
"protein_id": "ENSP00000533555.1",
"transcript_support_level": null,
"aa_start": 291,
"aa_end": null,
"aa_length": 545,
"cds_start": 871,
"cds_end": null,
"cds_length": 1638,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000863496.1"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FUBP3",
"gene_hgnc_id": 4005,
"hgvs_c": "c.814C>T",
"hgvs_p": "p.Pro272Ser",
"transcript": "ENST00000964143.1",
"protein_id": "ENSP00000634202.1",
"transcript_support_level": null,
"aa_start": 272,
"aa_end": null,
"aa_length": 529,
"cds_start": 814,
"cds_end": null,
"cds_length": 1590,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000964143.1"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FUBP3",
"gene_hgnc_id": 4005,
"hgvs_c": "c.871C>T",
"hgvs_p": "p.Pro291Ser",
"transcript": "ENST00000936134.1",
"protein_id": "ENSP00000606193.1",
"transcript_support_level": null,
"aa_start": 291,
"aa_end": null,
"aa_length": 521,
"cds_start": 871,
"cds_end": null,
"cds_length": 1566,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000936134.1"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FUBP3",
"gene_hgnc_id": 4005,
"hgvs_c": "c.871C>T",
"hgvs_p": "p.Pro291Ser",
"transcript": "ENST00000863498.1",
"protein_id": "ENSP00000533557.1",
"transcript_support_level": null,
"aa_start": 291,
"aa_end": null,
"aa_length": 417,
"cds_start": 871,
"cds_end": null,
"cds_length": 1254,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000863498.1"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FUBP3",
"gene_hgnc_id": 4005,
"hgvs_c": "c.289C>T",
"hgvs_p": "p.Pro97Ser",
"transcript": "ENST00000964146.1",
"protein_id": "ENSP00000634205.1",
"transcript_support_level": null,
"aa_start": 97,
"aa_end": null,
"aa_length": 378,
"cds_start": 289,
"cds_end": null,
"cds_length": 1137,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000964146.1"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FUBP3",
"gene_hgnc_id": 4005,
"hgvs_c": "c.871C>T",
"hgvs_p": "p.Pro291Ser",
"transcript": "XM_005272232.3",
"protein_id": "XP_005272289.1",
"transcript_support_level": null,
"aa_start": 291,
"aa_end": null,
"aa_length": 548,
"cds_start": 871,
"cds_end": null,
"cds_length": 1647,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_005272232.3"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FUBP3",
"gene_hgnc_id": 4005,
"hgvs_c": "c.871C>T",
"hgvs_p": "p.Pro291Ser",
"transcript": "XM_011519172.4",
"protein_id": "XP_011517474.1",
"transcript_support_level": null,
"aa_start": 291,
"aa_end": null,
"aa_length": 514,
"cds_start": 871,
"cds_end": null,
"cds_length": 1545,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011519172.4"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FUBP3",
"gene_hgnc_id": 4005,
"hgvs_c": "n.145C>T",
"hgvs_p": null,
"transcript": "ENST00000487406.2",
"protein_id": null,
"transcript_support_level": 5,
"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": "pseudogene",
"feature": "ENST00000487406.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FUBP3",
"gene_hgnc_id": 4005,
"hgvs_c": "n.*2687C>T",
"hgvs_p": null,
"transcript": "ENST00000650723.1",
"protein_id": "ENSP00000499109.1",
"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": "ENST00000650723.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FUBP3",
"gene_hgnc_id": 4005,
"hgvs_c": "n.*756C>T",
"hgvs_p": null,
"transcript": "ENST00000699747.1",
"protein_id": "ENSP00000514557.1",
"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": "ENST00000699747.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FUBP3",
"gene_hgnc_id": 4005,
"hgvs_c": "n.975C>T",
"hgvs_p": null,
"transcript": "XR_007061369.1",
"protein_id": null,
"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": "pseudogene",
"feature": "XR_007061369.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FUBP3",
"gene_hgnc_id": 4005,
"hgvs_c": "n.*2687C>T",
"hgvs_p": null,
"transcript": "ENST00000650723.1",
"protein_id": "ENSP00000499109.1",
"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": "ENST00000650723.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FUBP3",
"gene_hgnc_id": 4005,
"hgvs_c": "n.*756C>T",
"hgvs_p": null,
"transcript": "ENST00000699747.1",
"protein_id": "ENSP00000514557.1",
"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": "ENST00000699747.1"
}
],
"gene_symbol": "FUBP3",
"gene_hgnc_id": 4005,
"dbsnp": "rs1434334245",
"frequency_reference_population": 0.0000066350835,
"hom_count_reference_population": 0,
"allele_count_reference_population": 1,
"gnomad_exomes_af": 0,
"gnomad_genomes_af": 0.00000663508,
"gnomad_exomes_ac": 0,
"gnomad_genomes_ac": 1,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.4468511641025543,
"computational_prediction_selected": "Uncertain_significance",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.227,
"revel_prediction": "Benign",
"alphamissense_score": 0.1929,
"alphamissense_prediction": "Benign",
"bayesdelnoaf_score": -0.4,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 5.931,
"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": 2,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2",
"acmg_by_gene": [
{
"score": 2,
"benign_score": 0,
"pathogenic_score": 2,
"criteria": [
"PM2"
],
"verdict": "Uncertain_significance",
"transcript": "NM_003934.2",
"gene_symbol": "FUBP3",
"hgnc_id": 4005,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.871C>T",
"hgvs_p": "p.Pro291Ser"
}
],
"clinvar_disease": "not specified",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "not specified",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}