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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: 7-36855687-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=36855687&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "7",
"pos": 36855687,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_014800.11",
"consequences": [
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO1",
"gene_hgnc_id": 16286,
"hgvs_c": "c.2048G>A",
"hgvs_p": "p.Arg683Gln",
"transcript": "NM_014800.11",
"protein_id": "NP_055615.8",
"transcript_support_level": null,
"aa_start": 683,
"aa_end": null,
"aa_length": 727,
"cds_start": 2048,
"cds_end": null,
"cds_length": 2184,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000310758.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_014800.11"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO1",
"gene_hgnc_id": 16286,
"hgvs_c": "c.2048G>A",
"hgvs_p": "p.Arg683Gln",
"transcript": "ENST00000310758.9",
"protein_id": "ENSP00000312185.4",
"transcript_support_level": 1,
"aa_start": 683,
"aa_end": null,
"aa_length": 727,
"cds_start": 2048,
"cds_end": null,
"cds_length": 2184,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_014800.11",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000310758.9"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO1",
"gene_hgnc_id": 16286,
"hgvs_c": "c.2048G>A",
"hgvs_p": "p.Arg683Gln",
"transcript": "ENST00000448602.5",
"protein_id": "ENSP00000394458.1",
"transcript_support_level": 1,
"aa_start": 683,
"aa_end": null,
"aa_length": 727,
"cds_start": 2048,
"cds_end": null,
"cds_length": 2184,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000448602.5"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO1",
"gene_hgnc_id": 16286,
"hgvs_c": "c.608G>A",
"hgvs_p": "p.Arg203Gln",
"transcript": "ENST00000396040.6",
"protein_id": "ENSP00000379355.2",
"transcript_support_level": 1,
"aa_start": 203,
"aa_end": null,
"aa_length": 247,
"cds_start": 608,
"cds_end": null,
"cds_length": 744,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000396040.6"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO1",
"gene_hgnc_id": 16286,
"hgvs_c": "c.608G>A",
"hgvs_p": "p.Arg203Gln",
"transcript": "ENST00000396045.7",
"protein_id": "ENSP00000379360.3",
"transcript_support_level": 1,
"aa_start": 203,
"aa_end": null,
"aa_length": 247,
"cds_start": 608,
"cds_end": null,
"cds_length": 744,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000396045.7"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO1",
"gene_hgnc_id": 16286,
"hgvs_c": "c.2048G>A",
"hgvs_p": "p.Arg683Gln",
"transcript": "NM_001206480.2",
"protein_id": "NP_001193409.1",
"transcript_support_level": null,
"aa_start": 683,
"aa_end": null,
"aa_length": 727,
"cds_start": 2048,
"cds_end": null,
"cds_length": 2184,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001206480.2"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO1",
"gene_hgnc_id": 16286,
"hgvs_c": "c.2048G>A",
"hgvs_p": "p.Arg683Gln",
"transcript": "NM_001206482.2",
"protein_id": "NP_001193411.1",
"transcript_support_level": null,
"aa_start": 683,
"aa_end": null,
"aa_length": 727,
"cds_start": 2048,
"cds_end": null,
"cds_length": 2184,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001206482.2"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO1",
"gene_hgnc_id": 16286,
"hgvs_c": "c.2048G>A",
"hgvs_p": "p.Arg683Gln",
"transcript": "ENST00000442504.5",
"protein_id": "ENSP00000406952.1",
"transcript_support_level": 2,
"aa_start": 683,
"aa_end": null,
"aa_length": 727,
"cds_start": 2048,
"cds_end": null,
"cds_length": 2184,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000442504.5"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO1",
"gene_hgnc_id": 16286,
"hgvs_c": "c.2048G>A",
"hgvs_p": "p.Arg683Gln",
"transcript": "ENST00000898965.1",
"protein_id": "ENSP00000569024.1",
"transcript_support_level": null,
"aa_start": 683,
"aa_end": null,
"aa_length": 727,
"cds_start": 2048,
"cds_end": null,
"cds_length": 2184,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000898965.1"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO1",
"gene_hgnc_id": 16286,
"hgvs_c": "c.2048G>A",
"hgvs_p": "p.Arg683Gln",
"transcript": "ENST00000898966.1",
"protein_id": "ENSP00000569025.1",
"transcript_support_level": null,
"aa_start": 683,
"aa_end": null,
"aa_length": 727,
"cds_start": 2048,
"cds_end": null,
"cds_length": 2184,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000898966.1"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO1",
"gene_hgnc_id": 16286,
"hgvs_c": "c.2048G>A",
"hgvs_p": "p.Arg683Gln",
"transcript": "ENST00000898967.1",
"protein_id": "ENSP00000569026.1",
"transcript_support_level": null,
"aa_start": 683,
"aa_end": null,
"aa_length": 727,
"cds_start": 2048,
"cds_end": null,
"cds_length": 2184,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000898967.1"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO1",
"gene_hgnc_id": 16286,
"hgvs_c": "c.2048G>A",
"hgvs_p": "p.Arg683Gln",
"transcript": "ENST00000898968.1",
"protein_id": "ENSP00000569027.1",
"transcript_support_level": null,
"aa_start": 683,
"aa_end": null,
"aa_length": 727,
"cds_start": 2048,
"cds_end": null,
"cds_length": 2184,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000898968.1"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO1",
"gene_hgnc_id": 16286,
"hgvs_c": "c.2048G>A",
"hgvs_p": "p.Arg683Gln",
"transcript": "ENST00000898969.1",
"protein_id": "ENSP00000569028.1",
"transcript_support_level": null,
"aa_start": 683,
"aa_end": null,
"aa_length": 727,
"cds_start": 2048,
"cds_end": null,
"cds_length": 2184,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000898969.1"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO1",
"gene_hgnc_id": 16286,
"hgvs_c": "c.2048G>A",
"hgvs_p": "p.Arg683Gln",
"transcript": "ENST00000898970.1",
"protein_id": "ENSP00000569029.1",
"transcript_support_level": null,
"aa_start": 683,
"aa_end": null,
"aa_length": 727,
"cds_start": 2048,
"cds_end": null,
"cds_length": 2184,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000898970.1"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO1",
"gene_hgnc_id": 16286,
"hgvs_c": "c.2048G>A",
"hgvs_p": "p.Arg683Gln",
"transcript": "ENST00000963263.1",
"protein_id": "ENSP00000633322.1",
"transcript_support_level": null,
"aa_start": 683,
"aa_end": null,
"aa_length": 727,
"cds_start": 2048,
"cds_end": null,
"cds_length": 2184,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000963263.1"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO1",
"gene_hgnc_id": 16286,
"hgvs_c": "c.1940G>A",
"hgvs_p": "p.Arg647Gln",
"transcript": "ENST00000898964.1",
"protein_id": "ENSP00000569023.1",
"transcript_support_level": null,
"aa_start": 647,
"aa_end": null,
"aa_length": 691,
"cds_start": 1940,
"cds_end": null,
"cds_length": 2076,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000898964.1"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO1",
"gene_hgnc_id": 16286,
"hgvs_c": "c.608G>A",
"hgvs_p": "p.Arg203Gln",
"transcript": "NM_001039459.3",
"protein_id": "NP_001034548.1",
"transcript_support_level": null,
"aa_start": 203,
"aa_end": null,
"aa_length": 247,
"cds_start": 608,
"cds_end": null,
"cds_length": 744,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001039459.3"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO1",
"gene_hgnc_id": 16286,
"hgvs_c": "c.608G>A",
"hgvs_p": "p.Arg203Gln",
"transcript": "NM_130442.4",
"protein_id": "NP_569709.1",
"transcript_support_level": null,
"aa_start": 203,
"aa_end": null,
"aa_length": 247,
"cds_start": 608,
"cds_end": null,
"cds_length": 744,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_130442.4"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO1",
"gene_hgnc_id": 16286,
"hgvs_c": "c.2048G>A",
"hgvs_p": "p.Arg683Gln",
"transcript": "XM_005249919.4",
"protein_id": "XP_005249976.1",
"transcript_support_level": null,
"aa_start": 683,
"aa_end": null,
"aa_length": 727,
"cds_start": 2048,
"cds_end": null,
"cds_length": 2184,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_005249919.4"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO1",
"gene_hgnc_id": 16286,
"hgvs_c": "c.2048G>A",
"hgvs_p": "p.Arg683Gln",
"transcript": "XM_006715805.2",
"protein_id": "XP_006715868.1",
"transcript_support_level": null,
"aa_start": 683,
"aa_end": null,
"aa_length": 727,
"cds_start": 2048,
"cds_end": null,
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"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_006715805.2"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO1",
"gene_hgnc_id": 16286,
"hgvs_c": "c.2048G>A",
"hgvs_p": "p.Arg683Gln",
"transcript": "XM_011515654.3",
"protein_id": "XP_011513956.1",
"transcript_support_level": null,
"aa_start": 683,
"aa_end": null,
"aa_length": 727,
"cds_start": 2048,
"cds_end": null,
"cds_length": 2184,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011515654.3"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELMO1",
"gene_hgnc_id": 16286,
"hgvs_c": "c.2048G>A",
"hgvs_p": "p.Arg683Gln",
"transcript": "XM_017012839.2",
"protein_id": "XP_016868328.1",
"transcript_support_level": null,
"aa_start": 683,
"aa_end": null,
"aa_length": 727,
"cds_start": 2048,
"cds_end": null,
"cds_length": 2184,
"cdna_start": null,
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"cdna_length": null,
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{
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},
{
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"feature": "XM_047421086.1"
},
{
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],
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},
{
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],
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},
{
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"non_coding_transcript_exon_variant"
],
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"feature": "ENST00000487843.1"
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{
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],
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"biotype": "retained_intron",
"feature": "ENST00000497024.1"
},
{
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"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
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"gene_symbol": "ELMO1",
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"hgvs_c": "n.709G>A",
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"transcript": "NR_038120.2",
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"biotype": "pseudogene",
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],
"gene_symbol": "ELMO1",
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"dbsnp": "rs201616410",
"frequency_reference_population": 0.0001660508,
"hom_count_reference_population": 0,
"allele_count_reference_population": 268,
"gnomad_exomes_af": 0.00017102,
"gnomad_genomes_af": 0.000118307,
"gnomad_exomes_ac": 250,
"gnomad_genomes_ac": 18,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.03628450632095337,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.106,
"revel_prediction": "Benign",
"alphamissense_score": 0.0953,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.48,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 1.623,
"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": "Likely_benign",
"acmg_criteria": "BP4_Strong",
"acmg_by_gene": [
{
"score": -4,
"benign_score": 4,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong"
],
"verdict": "Likely_benign",
"transcript": "NM_014800.11",
"gene_symbol": "ELMO1",
"hgnc_id": 16286,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.2048G>A",
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}
],
"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
}