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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: 20-1980652-T-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=20&pos=1980652&ref=T&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "20",
"pos": 1980652,
"ref": "T",
"alt": "G",
"effect": "missense_variant",
"transcript": "ENST00000217305.3",
"consequences": [
{
"aa_ref": "M",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDYN",
"gene_hgnc_id": 8820,
"hgvs_c": "c.436A>C",
"hgvs_p": "p.Met146Leu",
"transcript": "NM_024411.5",
"protein_id": "NP_077722.1",
"transcript_support_level": null,
"aa_start": 146,
"aa_end": null,
"aa_length": 254,
"cds_start": 436,
"cds_end": null,
"cds_length": 765,
"cdna_start": 663,
"cdna_end": null,
"cdna_length": 2556,
"mane_select": "ENST00000217305.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "L",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDYN",
"gene_hgnc_id": 8820,
"hgvs_c": "c.436A>C",
"hgvs_p": "p.Met146Leu",
"transcript": "ENST00000217305.3",
"protein_id": "ENSP00000217305.2",
"transcript_support_level": 1,
"aa_start": 146,
"aa_end": null,
"aa_length": 254,
"cds_start": 436,
"cds_end": null,
"cds_length": 765,
"cdna_start": 663,
"cdna_end": null,
"cdna_length": 2556,
"mane_select": "NM_024411.5",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDYN",
"gene_hgnc_id": 8820,
"hgvs_c": "c.436A>C",
"hgvs_p": "p.Met146Leu",
"transcript": "NM_001190892.1",
"protein_id": "NP_001177821.1",
"transcript_support_level": null,
"aa_start": 146,
"aa_end": null,
"aa_length": 254,
"cds_start": 436,
"cds_end": null,
"cds_length": 765,
"cdna_start": 678,
"cdna_end": null,
"cdna_length": 2574,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDYN",
"gene_hgnc_id": 8820,
"hgvs_c": "c.436A>C",
"hgvs_p": "p.Met146Leu",
"transcript": "NM_001190898.3",
"protein_id": "NP_001177827.1",
"transcript_support_level": null,
"aa_start": 146,
"aa_end": null,
"aa_length": 254,
"cds_start": 436,
"cds_end": null,
"cds_length": 765,
"cdna_start": 660,
"cdna_end": null,
"cdna_length": 2553,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDYN",
"gene_hgnc_id": 8820,
"hgvs_c": "c.436A>C",
"hgvs_p": "p.Met146Leu",
"transcript": "NM_001190899.2",
"protein_id": "NP_001177828.1",
"transcript_support_level": null,
"aa_start": 146,
"aa_end": null,
"aa_length": 254,
"cds_start": 436,
"cds_end": null,
"cds_length": 765,
"cdna_start": 830,
"cdna_end": null,
"cdna_length": 2726,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDYN",
"gene_hgnc_id": 8820,
"hgvs_c": "c.436A>C",
"hgvs_p": "p.Met146Leu",
"transcript": "NM_001190900.1",
"protein_id": "NP_001177829.1",
"transcript_support_level": null,
"aa_start": 146,
"aa_end": null,
"aa_length": 254,
"cds_start": 436,
"cds_end": null,
"cds_length": 765,
"cdna_start": 577,
"cdna_end": null,
"cdna_length": 2473,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDYN",
"gene_hgnc_id": 8820,
"hgvs_c": "c.436A>C",
"hgvs_p": "p.Met146Leu",
"transcript": "ENST00000539905.5",
"protein_id": "ENSP00000440185.1",
"transcript_support_level": 4,
"aa_start": 146,
"aa_end": null,
"aa_length": 254,
"cds_start": 436,
"cds_end": null,
"cds_length": 765,
"cdna_start": 830,
"cdna_end": null,
"cdna_length": 2725,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDYN",
"gene_hgnc_id": 8820,
"hgvs_c": "c.436A>C",
"hgvs_p": "p.Met146Leu",
"transcript": "ENST00000540134.5",
"protein_id": "ENSP00000442259.1",
"transcript_support_level": 4,
"aa_start": 146,
"aa_end": null,
"aa_length": 254,
"cds_start": 436,
"cds_end": null,
"cds_length": 765,
"cdna_start": 577,
"cdna_end": null,
"cdna_length": 2472,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDYN",
"gene_hgnc_id": 8820,
"hgvs_c": "c.436A>C",
"hgvs_p": "p.Met146Leu",
"transcript": "ENST00000651328.1",
"protein_id": "ENSP00000499191.1",
"transcript_support_level": null,
"aa_start": 146,
"aa_end": null,
"aa_length": 148,
"cds_start": 436,
"cds_end": null,
"cds_length": 448,
"cdna_start": 570,
"cdna_end": null,
"cdna_length": 582,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDYN",
"gene_hgnc_id": 8820,
"hgvs_c": "c.436A>C",
"hgvs_p": "p.Met146Leu",
"transcript": "XM_011529244.2",
"protein_id": "XP_011527546.1",
"transcript_support_level": null,
"aa_start": 146,
"aa_end": null,
"aa_length": 254,
"cds_start": 436,
"cds_end": null,
"cds_length": 765,
"cdna_start": 571,
"cdna_end": null,
"cdna_length": 2467,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDYN",
"gene_hgnc_id": 8820,
"hgvs_c": "c.436A>C",
"hgvs_p": "p.Met146Leu",
"transcript": "XM_011529245.1",
"protein_id": "XP_011527547.1",
"transcript_support_level": null,
"aa_start": 146,
"aa_end": null,
"aa_length": 254,
"cds_start": 436,
"cds_end": null,
"cds_length": 765,
"cdna_start": 761,
"cdna_end": null,
"cdna_length": 2657,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDYN",
"gene_hgnc_id": 8820,
"hgvs_c": "c.436A>C",
"hgvs_p": "p.Met146Leu",
"transcript": "XM_011529246.3",
"protein_id": "XP_011527548.1",
"transcript_support_level": null,
"aa_start": 146,
"aa_end": null,
"aa_length": 254,
"cds_start": 436,
"cds_end": null,
"cds_length": 765,
"cdna_start": 578,
"cdna_end": null,
"cdna_length": 2474,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDYN",
"gene_hgnc_id": 8820,
"hgvs_c": "c.436A>C",
"hgvs_p": "p.Met146Leu",
"transcript": "XM_011529247.1",
"protein_id": "XP_011527549.1",
"transcript_support_level": null,
"aa_start": 146,
"aa_end": null,
"aa_length": 254,
"cds_start": 436,
"cds_end": null,
"cds_length": 765,
"cdna_start": 557,
"cdna_end": null,
"cdna_length": 2453,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDYN",
"gene_hgnc_id": 8820,
"hgvs_c": "c.436A>C",
"hgvs_p": "p.Met146Leu",
"transcript": "XM_011529248.2",
"protein_id": "XP_011527550.1",
"transcript_support_level": null,
"aa_start": 146,
"aa_end": null,
"aa_length": 254,
"cds_start": 436,
"cds_end": null,
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"cdna_start": 893,
"cdna_end": null,
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"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDYN",
"gene_hgnc_id": 8820,
"hgvs_c": "c.436A>C",
"hgvs_p": "p.Met146Leu",
"transcript": "XM_011529249.3",
"protein_id": "XP_011527551.1",
"transcript_support_level": null,
"aa_start": 146,
"aa_end": null,
"aa_length": 254,
"cds_start": 436,
"cds_end": null,
"cds_length": 765,
"cdna_start": 1299,
"cdna_end": null,
"cdna_length": 3195,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDYN",
"gene_hgnc_id": 8820,
"hgvs_c": "c.436A>C",
"hgvs_p": "p.Met146Leu",
"transcript": "XM_011529250.3",
"protein_id": "XP_011527552.1",
"transcript_support_level": null,
"aa_start": 146,
"aa_end": null,
"aa_length": 254,
"cds_start": 436,
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"cdna_start": 500,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDYN",
"gene_hgnc_id": 8820,
"hgvs_c": "c.436A>C",
"hgvs_p": "p.Met146Leu",
"transcript": "XM_017027878.1",
"protein_id": "XP_016883367.1",
"transcript_support_level": null,
"aa_start": 146,
"aa_end": null,
"aa_length": 254,
"cds_start": 436,
"cds_end": null,
"cds_length": 765,
"cdna_start": 560,
"cdna_end": null,
"cdna_length": 2456,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "PDYN-AS1",
"gene_hgnc_id": 53462,
"hgvs_c": "n.1216+14309T>G",
"hgvs_p": null,
"transcript": "ENST00000446562.1",
"protein_id": null,
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
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"cdna_length": 1802,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "PDYN-AS1",
"gene_hgnc_id": 53462,
"hgvs_c": "n.475+14309T>G",
"hgvs_p": null,
"transcript": "ENST00000651021.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
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"aa_length": null,
"cds_start": -4,
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"cdna_start": null,
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"feature": null
},
{
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"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "PDYN-AS1",
"gene_hgnc_id": 53462,
"hgvs_c": "n.1252+14309T>G",
"hgvs_p": null,
"transcript": "NR_134520.1",
"protein_id": null,
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"aa_start": null,
"aa_end": null,
"aa_length": null,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDYN",
"gene_hgnc_id": 8820,
"hgvs_c": "c.*22A>C",
"hgvs_p": null,
"transcript": "ENST00000650824.1",
"protein_id": "ENSP00000499095.1",
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"cds_start": -4,
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"cdna_start": null,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDYN",
"gene_hgnc_id": 8820,
"hgvs_c": "c.*80A>C",
"hgvs_p": null,
"transcript": "ENST00000651882.1",
"protein_id": "ENSP00000498752.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 117,
"cds_start": -4,
"cds_end": null,
"cds_length": 356,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 807,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDYN",
"gene_hgnc_id": 8820,
"hgvs_c": "c.*89A>C",
"hgvs_p": null,
"transcript": "ENST00000650937.1",
"protein_id": "ENSP00000498947.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 114,
"cds_start": -4,
"cds_end": null,
"cds_length": 347,
"cdna_start": null,
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"cdna_length": 589,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
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"gene_symbol": "PDYN",
"gene_hgnc_id": 8820,
"hgvs_c": "c.*163A>C",
"hgvs_p": null,
"transcript": "ENST00000651684.1",
"protein_id": "ENSP00000498453.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 90,
"cds_start": -4,
"cds_end": null,
"cds_length": 273,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 464,
"mane_select": null,
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"biotype": null,
"feature": null
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDYN",
"gene_hgnc_id": 8820,
"hgvs_c": "c.*168A>C",
"hgvs_p": null,
"transcript": "ENST00000650874.1",
"protein_id": "ENSP00000498438.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 88,
"cds_start": -4,
"cds_end": null,
"cds_length": 268,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 465,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDYN",
"gene_hgnc_id": 8820,
"hgvs_c": "c.*231A>C",
"hgvs_p": null,
"transcript": "ENST00000652436.1",
"protein_id": "ENSP00000499024.1",
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"aa_start": null,
"aa_end": null,
"aa_length": 67,
"cds_start": -4,
"cds_end": null,
"cds_length": 205,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 530,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "PDYN",
"gene_hgnc_id": 8820,
"dbsnp": "rs77155664",
"frequency_reference_population": 0.0067304773,
"hom_count_reference_population": 64,
"allele_count_reference_population": 10864,
"gnomad_exomes_af": 0.00690075,
"gnomad_genomes_af": 0.00509588,
"gnomad_exomes_ac": 10088,
"gnomad_genomes_ac": 776,
"gnomad_exomes_homalt": 61,
"gnomad_genomes_homalt": 3,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.00405922532081604,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.122,
"revel_prediction": "Benign",
"alphamissense_score": 0.0764,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.58,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -2.411,
"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": -16,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6_Very_Strong,BS2",
"acmg_by_gene": [
{
"score": -16,
"benign_score": 16,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong",
"BS2"
],
"verdict": "Benign",
"transcript": "ENST00000217305.3",
"gene_symbol": "PDYN",
"hgnc_id": 8820,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.436A>C",
"hgvs_p": "p.Met146Leu"
},
{
"score": -16,
"benign_score": 16,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong",
"BS2"
],
"verdict": "Benign",
"transcript": "ENST00000446562.1",
"gene_symbol": "PDYN-AS1",
"hgnc_id": 53462,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.1216+14309T>G",
"hgvs_p": null
}
],
"clinvar_disease": "Spinocerebellar ataxia type 23,not provided,not specified",
"clinvar_classification": "Benign/Likely benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "LB:5 B:3",
"phenotype_combined": "not provided|Spinocerebellar ataxia type 23|not specified",
"pathogenicity_classification_combined": "Benign/Likely benign",
"custom_annotations": null
}
],
"message": null
}