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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: 19-1073566-C-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=19&pos=1073566&ref=C&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "19",
"pos": 1073566,
"ref": "C",
"alt": "G",
"effect": "missense_variant",
"transcript": "NM_001258328.4",
"consequences": [
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ARHGAP45",
"gene_hgnc_id": 17102,
"hgvs_c": "c.626C>G",
"hgvs_p": "p.Thr209Arg",
"transcript": "NM_012292.5",
"protein_id": "NP_036424.2",
"transcript_support_level": null,
"aa_start": 209,
"aa_end": null,
"aa_length": 1136,
"cds_start": 626,
"cds_end": null,
"cds_length": 3411,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000313093.7",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_012292.5"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ARHGAP45",
"gene_hgnc_id": 17102,
"hgvs_c": "c.626C>G",
"hgvs_p": "p.Thr209Arg",
"transcript": "ENST00000313093.7",
"protein_id": "ENSP00000316772.2",
"transcript_support_level": 1,
"aa_start": 209,
"aa_end": null,
"aa_length": 1136,
"cds_start": 626,
"cds_end": null,
"cds_length": 3411,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_012292.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000313093.7"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ARHGAP45",
"gene_hgnc_id": 17102,
"hgvs_c": "c.638C>G",
"hgvs_p": "p.Thr213Arg",
"transcript": "ENST00000586866.5",
"protein_id": "ENSP00000468615.1",
"transcript_support_level": 1,
"aa_start": 213,
"aa_end": null,
"aa_length": 1140,
"cds_start": 638,
"cds_end": null,
"cds_length": 3423,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000586866.5"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ARHGAP45",
"gene_hgnc_id": 17102,
"hgvs_c": "c.626C>G",
"hgvs_p": "p.Thr209Arg",
"transcript": "ENST00000885660.1",
"protein_id": "ENSP00000555719.1",
"transcript_support_level": null,
"aa_start": 209,
"aa_end": null,
"aa_length": 1164,
"cds_start": 626,
"cds_end": null,
"cds_length": 3495,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000885660.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ARHGAP45",
"gene_hgnc_id": 17102,
"hgvs_c": "c.707C>G",
"hgvs_p": "p.Thr236Arg",
"transcript": "ENST00000590214.5",
"protein_id": "ENSP00000466401.1",
"transcript_support_level": 5,
"aa_start": 236,
"aa_end": null,
"aa_length": 1163,
"cds_start": 707,
"cds_end": null,
"cds_length": 3492,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000590214.5"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ARHGAP45",
"gene_hgnc_id": 17102,
"hgvs_c": "c.626C>G",
"hgvs_p": "p.Thr209Arg",
"transcript": "ENST00000964187.1",
"protein_id": "ENSP00000634246.1",
"transcript_support_level": null,
"aa_start": 209,
"aa_end": null,
"aa_length": 1159,
"cds_start": 626,
"cds_end": null,
"cds_length": 3480,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000964187.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ARHGAP45",
"gene_hgnc_id": 17102,
"hgvs_c": "c.674C>G",
"hgvs_p": "p.Thr225Arg",
"transcript": "NM_001258328.4",
"protein_id": "NP_001245257.1",
"transcript_support_level": null,
"aa_start": 225,
"aa_end": null,
"aa_length": 1152,
"cds_start": 674,
"cds_end": null,
"cds_length": 3459,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001258328.4"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ARHGAP45",
"gene_hgnc_id": 17102,
"hgvs_c": "c.674C>G",
"hgvs_p": "p.Thr225Arg",
"transcript": "ENST00000539243.6",
"protein_id": "ENSP00000439601.1",
"transcript_support_level": 2,
"aa_start": 225,
"aa_end": null,
"aa_length": 1152,
"cds_start": 674,
"cds_end": null,
"cds_length": 3459,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000539243.6"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ARHGAP45",
"gene_hgnc_id": 17102,
"hgvs_c": "c.638C>G",
"hgvs_p": "p.Thr213Arg",
"transcript": "NM_001321232.2",
"protein_id": "NP_001308161.1",
"transcript_support_level": null,
"aa_start": 213,
"aa_end": null,
"aa_length": 1140,
"cds_start": 638,
"cds_end": null,
"cds_length": 3423,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001321232.2"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ARHGAP45",
"gene_hgnc_id": 17102,
"hgvs_c": "c.629C>G",
"hgvs_p": "p.Thr210Arg",
"transcript": "ENST00000885658.1",
"protein_id": "ENSP00000555717.1",
"transcript_support_level": null,
"aa_start": 210,
"aa_end": null,
"aa_length": 1137,
"cds_start": 629,
"cds_end": null,
"cds_length": 3414,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000885658.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ARHGAP45",
"gene_hgnc_id": 17102,
"hgvs_c": "c.611C>G",
"hgvs_p": "p.Thr204Arg",
"transcript": "ENST00000885662.1",
"protein_id": "ENSP00000555721.1",
"transcript_support_level": null,
"aa_start": 204,
"aa_end": null,
"aa_length": 1131,
"cds_start": 611,
"cds_end": null,
"cds_length": 3396,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000885662.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ARHGAP45",
"gene_hgnc_id": 17102,
"hgvs_c": "c.626C>G",
"hgvs_p": "p.Thr209Arg",
"transcript": "ENST00000885661.1",
"protein_id": "ENSP00000555720.1",
"transcript_support_level": null,
"aa_start": 209,
"aa_end": null,
"aa_length": 1121,
"cds_start": 626,
"cds_end": null,
"cds_length": 3366,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000885661.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ARHGAP45",
"gene_hgnc_id": 17102,
"hgvs_c": "c.626C>G",
"hgvs_p": "p.Thr209Arg",
"transcript": "ENST00000885659.1",
"protein_id": "ENSP00000555718.1",
"transcript_support_level": null,
"aa_start": 209,
"aa_end": null,
"aa_length": 1108,
"cds_start": 626,
"cds_end": null,
"cds_length": 3327,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000885659.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ARHGAP45",
"gene_hgnc_id": 17102,
"hgvs_c": "c.275C>G",
"hgvs_p": "p.Thr92Arg",
"transcript": "NM_001282335.3",
"protein_id": "NP_001269264.1",
"transcript_support_level": null,
"aa_start": 92,
"aa_end": null,
"aa_length": 1019,
"cds_start": 275,
"cds_end": null,
"cds_length": 3060,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001282335.3"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ARHGAP45",
"gene_hgnc_id": 17102,
"hgvs_c": "c.275C>G",
"hgvs_p": "p.Thr92Arg",
"transcript": "ENST00000543365.5",
"protein_id": "ENSP00000438979.1",
"transcript_support_level": 2,
"aa_start": 92,
"aa_end": null,
"aa_length": 1019,
"cds_start": 275,
"cds_end": null,
"cds_length": 3060,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000543365.5"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ARHGAP45",
"gene_hgnc_id": 17102,
"hgvs_c": "c.674C>G",
"hgvs_p": "p.Thr225Arg",
"transcript": "XM_047438545.1",
"protein_id": "XP_047294501.1",
"transcript_support_level": null,
"aa_start": 225,
"aa_end": null,
"aa_length": 1180,
"cds_start": 674,
"cds_end": null,
"cds_length": 3543,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047438545.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ARHGAP45",
"gene_hgnc_id": 17102,
"hgvs_c": "c.638C>G",
"hgvs_p": "p.Thr213Arg",
"transcript": "XM_011527858.1",
"protein_id": "XP_011526160.1",
"transcript_support_level": null,
"aa_start": 213,
"aa_end": null,
"aa_length": 1168,
"cds_start": 638,
"cds_end": null,
"cds_length": 3507,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011527858.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ARHGAP45",
"gene_hgnc_id": 17102,
"hgvs_c": "c.626C>G",
"hgvs_p": "p.Thr209Arg",
"transcript": "XM_047438546.1",
"protein_id": "XP_047294502.1",
"transcript_support_level": null,
"aa_start": 209,
"aa_end": null,
"aa_length": 1164,
"cds_start": 626,
"cds_end": null,
"cds_length": 3495,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047438546.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ARHGAP45",
"gene_hgnc_id": 17102,
"hgvs_c": "c.638C>G",
"hgvs_p": "p.Thr213Arg",
"transcript": "XM_047438547.1",
"protein_id": "XP_047294503.1",
"transcript_support_level": null,
"aa_start": 213,
"aa_end": null,
"aa_length": 1140,
"cds_start": 638,
"cds_end": null,
"cds_length": 3423,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047438547.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ARHGAP45",
"gene_hgnc_id": 17102,
"hgvs_c": "c.626C>G",
"hgvs_p": "p.Thr209Arg",
"transcript": "XM_047438548.1",
"protein_id": "XP_047294504.1",
"transcript_support_level": null,
"aa_start": 209,
"aa_end": null,
"aa_length": 1136,
"cds_start": 626,
"cds_end": null,
"cds_length": 3411,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047438548.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ARHGAP45",
"gene_hgnc_id": 17102,
"hgvs_c": "n.*112C>G",
"hgvs_p": null,
"transcript": "ENST00000587602.5",
"protein_id": "ENSP00000466365.1",
"transcript_support_level": 2,
"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": "ENST00000587602.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ARHGAP45",
"gene_hgnc_id": 17102,
"hgvs_c": "n.*112C>G",
"hgvs_p": null,
"transcript": "ENST00000587602.5",
"protein_id": "ENSP00000466365.1",
"transcript_support_level": 2,
"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,
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{
"aa_ref": null,
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"canonical": false,
"protein_coding": false,
"strand": true,
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"intron_variant"
],
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{
"aa_ref": null,
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"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"upstream_gene_variant"
],
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"exon_count": 5,
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"gene_symbol": "ARHGAP45",
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"transcript": "ENST00000586033.1",
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"biotype": "retained_intron",
"feature": "ENST00000586033.1"
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{
"aa_ref": null,
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"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
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"exon_count": 3,
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"gene_symbol": "ARHGAP45",
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"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
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"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000592335.2"
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],
"gene_symbol": "ARHGAP45",
"gene_hgnc_id": 17102,
"dbsnp": "rs145027652",
"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": 0.8499212861061096,
"computational_prediction_selected": "Pathogenic",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.305,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.2018,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.1,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 3.641,
"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": 4,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,PP3_Moderate",
"acmg_by_gene": [
{
"score": 4,
"benign_score": 0,
"pathogenic_score": 4,
"criteria": [
"PM2",
"PP3_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "NM_001258328.4",
"gene_symbol": "ARHGAP45",
"hgnc_id": 17102,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.674C>G",
"hgvs_p": "p.Thr225Arg"
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}