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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: 19-10459733-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=19&pos=10459733&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "19",
"pos": 10459733,
"ref": "G",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_001111307.2",
"consequences": [
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4A",
"gene_hgnc_id": 8780,
"hgvs_c": "c.1339G>C",
"hgvs_p": "p.Val447Leu",
"transcript": "NM_001111307.2",
"protein_id": "NP_001104777.1",
"transcript_support_level": null,
"aa_start": 447,
"aa_end": null,
"aa_length": 886,
"cds_start": 1339,
"cds_end": null,
"cds_length": 2661,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000380702.7",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001111307.2"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4A",
"gene_hgnc_id": 8780,
"hgvs_c": "c.1339G>C",
"hgvs_p": "p.Val447Leu",
"transcript": "ENST00000380702.7",
"protein_id": "ENSP00000370078.3",
"transcript_support_level": 1,
"aa_start": 447,
"aa_end": null,
"aa_length": 886,
"cds_start": 1339,
"cds_end": null,
"cds_length": 2661,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001111307.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000380702.7"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4A",
"gene_hgnc_id": 8780,
"hgvs_c": "c.1273G>C",
"hgvs_p": "p.Val425Leu",
"transcript": "ENST00000592685.5",
"protein_id": "ENSP00000468507.1",
"transcript_support_level": 1,
"aa_start": 425,
"aa_end": null,
"aa_length": 864,
"cds_start": 1273,
"cds_end": null,
"cds_length": 2595,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000592685.5"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4A",
"gene_hgnc_id": 8780,
"hgvs_c": "c.1261G>C",
"hgvs_p": "p.Val421Leu",
"transcript": "ENST00000293683.9",
"protein_id": "ENSP00000293683.4",
"transcript_support_level": 1,
"aa_start": 421,
"aa_end": null,
"aa_length": 860,
"cds_start": 1261,
"cds_end": null,
"cds_length": 2583,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000293683.9"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4A",
"gene_hgnc_id": 8780,
"hgvs_c": "c.1156G>C",
"hgvs_p": "p.Val386Leu",
"transcript": "ENST00000440014.6",
"protein_id": "ENSP00000394754.1",
"transcript_support_level": 1,
"aa_start": 386,
"aa_end": null,
"aa_length": 825,
"cds_start": 1156,
"cds_end": null,
"cds_length": 2478,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000440014.6"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4A",
"gene_hgnc_id": 8780,
"hgvs_c": "c.622G>C",
"hgvs_p": "p.Val208Leu",
"transcript": "ENST00000344979.7",
"protein_id": "ENSP00000341007.2",
"transcript_support_level": 1,
"aa_start": 208,
"aa_end": null,
"aa_length": 647,
"cds_start": 622,
"cds_end": null,
"cds_length": 1944,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000344979.7"
},
{
"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": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4A",
"gene_hgnc_id": 8780,
"hgvs_c": "n.669G>C",
"hgvs_p": null,
"transcript": "ENST00000590407.1",
"protein_id": null,
"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": "retained_intron",
"feature": "ENST00000590407.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4A",
"gene_hgnc_id": 8780,
"hgvs_c": "c.1306G>C",
"hgvs_p": "p.Val436Leu",
"transcript": "ENST00000937031.1",
"protein_id": "ENSP00000607090.1",
"transcript_support_level": null,
"aa_start": 436,
"aa_end": null,
"aa_length": 875,
"cds_start": 1306,
"cds_end": null,
"cds_length": 2628,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000937031.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4A",
"gene_hgnc_id": 8780,
"hgvs_c": "c.1273G>C",
"hgvs_p": "p.Val425Leu",
"transcript": "NM_001243121.2",
"protein_id": "NP_001230050.1",
"transcript_support_level": null,
"aa_start": 425,
"aa_end": null,
"aa_length": 864,
"cds_start": 1273,
"cds_end": null,
"cds_length": 2595,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001243121.2"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4A",
"gene_hgnc_id": 8780,
"hgvs_c": "c.1261G>C",
"hgvs_p": "p.Val421Leu",
"transcript": "NM_001111308.1",
"protein_id": "NP_001104778.1",
"transcript_support_level": null,
"aa_start": 421,
"aa_end": null,
"aa_length": 860,
"cds_start": 1261,
"cds_end": null,
"cds_length": 2583,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001111308.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4A",
"gene_hgnc_id": 8780,
"hgvs_c": "c.1207G>C",
"hgvs_p": "p.Val403Leu",
"transcript": "ENST00000937030.1",
"protein_id": "ENSP00000607089.1",
"transcript_support_level": null,
"aa_start": 403,
"aa_end": null,
"aa_length": 842,
"cds_start": 1207,
"cds_end": null,
"cds_length": 2529,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000937030.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4A",
"gene_hgnc_id": 8780,
"hgvs_c": "c.1156G>C",
"hgvs_p": "p.Val386Leu",
"transcript": "NM_001111309.1",
"protein_id": "NP_001104779.1",
"transcript_support_level": null,
"aa_start": 386,
"aa_end": null,
"aa_length": 825,
"cds_start": 1156,
"cds_end": null,
"cds_length": 2478,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001111309.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4A",
"gene_hgnc_id": 8780,
"hgvs_c": "c.1147G>C",
"hgvs_p": "p.Val383Leu",
"transcript": "ENST00000875632.1",
"protein_id": "ENSP00000545691.1",
"transcript_support_level": null,
"aa_start": 383,
"aa_end": null,
"aa_length": 822,
"cds_start": 1147,
"cds_end": null,
"cds_length": 2469,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000875632.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4A",
"gene_hgnc_id": 8780,
"hgvs_c": "c.622G>C",
"hgvs_p": "p.Val208Leu",
"transcript": "NM_006202.3",
"protein_id": "NP_006193.1",
"transcript_support_level": null,
"aa_start": 208,
"aa_end": null,
"aa_length": 647,
"cds_start": 622,
"cds_end": null,
"cds_length": 1944,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_006202.3"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4A",
"gene_hgnc_id": 8780,
"hgvs_c": "c.1336G>C",
"hgvs_p": "p.Val446Leu",
"transcript": "XM_017026865.3",
"protein_id": "XP_016882354.1",
"transcript_support_level": null,
"aa_start": 446,
"aa_end": null,
"aa_length": 885,
"cds_start": 1336,
"cds_end": null,
"cds_length": 2658,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017026865.3"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4A",
"gene_hgnc_id": 8780,
"hgvs_c": "c.1270G>C",
"hgvs_p": "p.Val424Leu",
"transcript": "XM_047438910.1",
"protein_id": "XP_047294866.1",
"transcript_support_level": null,
"aa_start": 424,
"aa_end": null,
"aa_length": 863,
"cds_start": 1270,
"cds_end": null,
"cds_length": 2592,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047438910.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4A",
"gene_hgnc_id": 8780,
"hgvs_c": "c.1258G>C",
"hgvs_p": "p.Val420Leu",
"transcript": "XM_047438911.1",
"protein_id": "XP_047294867.1",
"transcript_support_level": null,
"aa_start": 420,
"aa_end": null,
"aa_length": 859,
"cds_start": 1258,
"cds_end": null,
"cds_length": 2580,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047438911.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4A",
"gene_hgnc_id": 8780,
"hgvs_c": "c.1153G>C",
"hgvs_p": "p.Val385Leu",
"transcript": "XM_047438912.1",
"protein_id": "XP_047294868.1",
"transcript_support_level": null,
"aa_start": 385,
"aa_end": null,
"aa_length": 824,
"cds_start": 1153,
"cds_end": null,
"cds_length": 2475,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047438912.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4A",
"gene_hgnc_id": 8780,
"hgvs_c": "c.1339G>C",
"hgvs_p": "p.Val447Leu",
"transcript": "XM_011528055.4",
"protein_id": "XP_011526357.1",
"transcript_support_level": null,
"aa_start": 447,
"aa_end": null,
"aa_length": 657,
"cds_start": 1339,
"cds_end": null,
"cds_length": 1974,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011528055.4"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4A",
"gene_hgnc_id": 8780,
"hgvs_c": "c.1261G>C",
"hgvs_p": "p.Val421Leu",
"transcript": "XM_047438913.1",
"protein_id": "XP_047294869.1",
"transcript_support_level": null,
"aa_start": 421,
"aa_end": null,
"aa_length": 631,
"cds_start": 1261,
"cds_end": null,
"cds_length": 1896,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047438913.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4A",
"gene_hgnc_id": 8780,
"hgvs_c": "c.1156G>C",
"hgvs_p": "p.Val386Leu",
"transcript": "XM_047438914.1",
"protein_id": "XP_047294870.1",
"transcript_support_level": null,
"aa_start": 386,
"aa_end": null,
"aa_length": 596,
"cds_start": 1156,
"cds_end": null,
"cds_length": 1791,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047438914.1"
},
{
"aa_ref": "V",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4A",
"gene_hgnc_id": 8780,
"hgvs_c": "c.427G>C",
"hgvs_p": "p.Val143Leu",
"transcript": "XM_047438915.1",
"protein_id": "XP_047294871.1",
"transcript_support_level": null,
"aa_start": 143,
"aa_end": null,
"aa_length": 582,
"cds_start": 427,
"cds_end": null,
"cds_length": 1749,
"cdna_start": null,
"cdna_end": null,
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{
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{
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{
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],
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"biotype": "retained_intron",
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],
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"dbsnp": "rs142235107",
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"hom_count_reference_population": 0,
"allele_count_reference_population": 1,
"gnomad_exomes_af": 6.84489e-7,
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"gnomad_exomes_ac": 1,
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"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.6837493181228638,
"computational_prediction_selected": "Uncertain_significance",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.376,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.6158,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.02,
"bayesdelnoaf_prediction": "Uncertain_significance",
"phylop100way_score": 6.677,
"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_001111307.2",
"gene_symbol": "PDE4A",
"hgnc_id": 8780,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.1339G>C",
"hgvs_p": "p.Val447Leu"
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],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}