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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: 6-29659566-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=6&pos=29659566&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "6",
"pos": 29659566,
"ref": "C",
"alt": "T",
"effect": "synonymous_variant",
"transcript": "NM_001363610.2",
"consequences": [
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOG",
"gene_hgnc_id": 7197,
"hgvs_c": "c.336C>T",
"hgvs_p": "p.Leu112Leu",
"transcript": "NM_206809.4",
"protein_id": "NP_996532.2",
"transcript_support_level": null,
"aa_start": 112,
"aa_end": null,
"aa_length": 247,
"cds_start": 336,
"cds_end": null,
"cds_length": 744,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000376917.8",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_206809.4"
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOG",
"gene_hgnc_id": 7197,
"hgvs_c": "c.336C>T",
"hgvs_p": "p.Leu112Leu",
"transcript": "ENST00000376917.8",
"protein_id": "ENSP00000366115.3",
"transcript_support_level": 1,
"aa_start": 112,
"aa_end": null,
"aa_length": 247,
"cds_start": 336,
"cds_end": null,
"cds_length": 744,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_206809.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000376917.8"
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOG",
"gene_hgnc_id": 7197,
"hgvs_c": "c.336C>T",
"hgvs_p": "p.Leu112Leu",
"transcript": "ENST00000376894.8",
"protein_id": "ENSP00000366091.4",
"transcript_support_level": 1,
"aa_start": 112,
"aa_end": null,
"aa_length": 295,
"cds_start": 336,
"cds_end": null,
"cds_length": 888,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000376894.8"
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOG",
"gene_hgnc_id": 7197,
"hgvs_c": "c.336C>T",
"hgvs_p": "p.Leu112Leu",
"transcript": "ENST00000376898.7",
"protein_id": "ENSP00000366095.3",
"transcript_support_level": 1,
"aa_start": 112,
"aa_end": null,
"aa_length": 252,
"cds_start": 336,
"cds_end": null,
"cds_length": 759,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000376898.7"
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOG",
"gene_hgnc_id": 7197,
"hgvs_c": "c.336C>T",
"hgvs_p": "p.Leu112Leu",
"transcript": "ENST00000494692.5",
"protein_id": "ENSP00000417405.1",
"transcript_support_level": 1,
"aa_start": 112,
"aa_end": null,
"aa_length": 229,
"cds_start": 336,
"cds_end": null,
"cds_length": 690,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000494692.5"
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOG",
"gene_hgnc_id": 7197,
"hgvs_c": "c.336C>T",
"hgvs_p": "p.Leu112Leu",
"transcript": "ENST00000396701.6",
"protein_id": "ENSP00000379929.2",
"transcript_support_level": 1,
"aa_start": 112,
"aa_end": null,
"aa_length": 213,
"cds_start": 336,
"cds_end": null,
"cds_length": 642,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000396701.6"
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOG",
"gene_hgnc_id": 7197,
"hgvs_c": "c.336C>T",
"hgvs_p": "p.Leu112Leu",
"transcript": "ENST00000376891.8",
"protein_id": "ENSP00000366088.4",
"transcript_support_level": 1,
"aa_start": 112,
"aa_end": null,
"aa_length": 206,
"cds_start": 336,
"cds_end": null,
"cds_length": 621,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000376891.8"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "MOG",
"gene_hgnc_id": 7197,
"hgvs_c": "c.88+2269C>T",
"hgvs_p": null,
"transcript": "ENST00000376888.6",
"protein_id": "ENSP00000366085.2",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 131,
"cds_start": null,
"cds_end": null,
"cds_length": 396,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000376888.6"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "MOG",
"gene_hgnc_id": 7197,
"hgvs_c": "c.88+2269C>T",
"hgvs_p": null,
"transcript": "ENST00000490427.5",
"protein_id": "ENSP00000420350.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 108,
"cds_start": null,
"cds_end": null,
"cds_length": 327,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000490427.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "MOG",
"gene_hgnc_id": 7197,
"hgvs_c": "c.88+2269C>T",
"hgvs_p": null,
"transcript": "ENST00000483013.5",
"protein_id": "ENSP00000418090.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 92,
"cds_start": null,
"cds_end": null,
"cds_length": 279,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000483013.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOG",
"gene_hgnc_id": 7197,
"hgvs_c": "n.246C>T",
"hgvs_p": null,
"transcript": "ENST00000376889.3",
"protein_id": "ENSP00000366086.3",
"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": "nonsense_mediated_decay",
"feature": "ENST00000376889.3"
},
{
"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": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOG",
"gene_hgnc_id": 7197,
"hgvs_c": "n.330C>T",
"hgvs_p": null,
"transcript": "ENST00000469603.1",
"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": "pseudogene",
"feature": "ENST00000469603.1"
},
{
"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": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOG",
"gene_hgnc_id": 7197,
"hgvs_c": "n.330C>T",
"hgvs_p": null,
"transcript": "ENST00000476244.5",
"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": "pseudogene",
"feature": "ENST00000476244.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOG",
"gene_hgnc_id": 7197,
"hgvs_c": "n.246C>T",
"hgvs_p": null,
"transcript": "ENST00000485211.5",
"protein_id": "ENSP00000418872.1",
"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": "nonsense_mediated_decay",
"feature": "ENST00000485211.5"
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOG",
"gene_hgnc_id": 7197,
"hgvs_c": "c.336C>T",
"hgvs_p": "p.Leu112Leu",
"transcript": "NM_001363610.2",
"protein_id": "NP_001350539.1",
"transcript_support_level": null,
"aa_start": 112,
"aa_end": null,
"aa_length": 295,
"cds_start": 336,
"cds_end": null,
"cds_length": 888,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001363610.2"
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOG",
"gene_hgnc_id": 7197,
"hgvs_c": "c.336C>T",
"hgvs_p": "p.Leu112Leu",
"transcript": "ENST00000963921.1",
"protein_id": "ENSP00000633980.1",
"transcript_support_level": null,
"aa_start": 112,
"aa_end": null,
"aa_length": 259,
"cds_start": 336,
"cds_end": null,
"cds_length": 780,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000963921.1"
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOG",
"gene_hgnc_id": 7197,
"hgvs_c": "c.336C>T",
"hgvs_p": "p.Leu112Leu",
"transcript": "NM_002433.5",
"protein_id": "NP_002424.3",
"transcript_support_level": null,
"aa_start": 112,
"aa_end": null,
"aa_length": 252,
"cds_start": 336,
"cds_end": null,
"cds_length": 759,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_002433.5"
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOG",
"gene_hgnc_id": 7197,
"hgvs_c": "c.336C>T",
"hgvs_p": "p.Leu112Leu",
"transcript": "ENST00000963920.1",
"protein_id": "ENSP00000633979.1",
"transcript_support_level": null,
"aa_start": 112,
"aa_end": null,
"aa_length": 247,
"cds_start": 336,
"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": "ENST00000963920.1"
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOG",
"gene_hgnc_id": 7197,
"hgvs_c": "c.336C>T",
"hgvs_p": "p.Leu112Leu",
"transcript": "NM_206811.4",
"protein_id": "NP_996534.2",
"transcript_support_level": null,
"aa_start": 112,
"aa_end": null,
"aa_length": 229,
"cds_start": 336,
"cds_end": null,
"cds_length": 690,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_206811.4"
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOG",
"gene_hgnc_id": 7197,
"hgvs_c": "c.336C>T",
"hgvs_p": "p.Leu112Leu",
"transcript": "NM_001008228.3",
"protein_id": "NP_001008229.1",
"transcript_support_level": null,
"aa_start": 112,
"aa_end": null,
"aa_length": 224,
"cds_start": 336,
"cds_end": null,
"cds_length": 675,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001008228.3"
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOG",
"gene_hgnc_id": 7197,
"hgvs_c": "c.336C>T",
"hgvs_p": "p.Leu112Leu",
"transcript": "ENST00000396704.7",
"protein_id": "ENSP00000379932.3",
"transcript_support_level": 5,
"aa_start": 112,
"aa_end": null,
"aa_length": 224,
"cds_start": 336,
"cds_end": null,
"cds_length": 675,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000396704.7"
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MOG",
"gene_hgnc_id": 7197,
"hgvs_c": "c.336C>T",
"hgvs_p": "p.Leu112Leu",
"transcript": "NM_206810.4",
"protein_id": "NP_996533.2",
"transcript_support_level": null,
"aa_start": 112,
"aa_end": null,
"aa_length": 213,
"cds_start": 336,
"cds_end": null,
"cds_length": 642,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_206810.4"
},
{
"aa_ref": "L",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
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{
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},
{
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},
{
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"feature": "NM_001008229.3"
},
{
"aa_ref": null,
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],
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},
{
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],
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"feature": "NM_001170418.2"
},
{
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],
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{
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],
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{
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"consequences": [
"3_prime_UTR_variant"
],
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"biotype": "nonsense_mediated_decay",
"feature": "ENST00000376903.4"
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],
"gene_symbol": "MOG",
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"dbsnp": "rs150910417",
"frequency_reference_population": 0.0009057117,
"hom_count_reference_population": 1,
"allele_count_reference_population": 1461,
"gnomad_exomes_af": 0.000928953,
"gnomad_genomes_af": 0.000682809,
"gnomad_exomes_ac": 1357,
"gnomad_genomes_ac": 104,
"gnomad_exomes_homalt": 1,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.5199999809265137,
"computational_prediction_selected": "Benign",
"computational_source_selected": "BayesDel_noAF",
"splice_score_selected": 0.009999999776482582,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.52,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.417,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0.01,
"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": -7,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6_Moderate,BP7",
"acmg_by_gene": [
{
"score": -7,
"benign_score": 7,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Moderate",
"BP7"
],
"verdict": "Benign",
"transcript": "NM_001363610.2",
"gene_symbol": "MOG",
"hgnc_id": 7197,
"effects": [
"synonymous_variant"
],
"inheritance_mode": "Unknown",
"hgvs_c": "c.336C>T",
"hgvs_p": "p.Leu112Leu"
}
],
"clinvar_disease": "not provided",
"clinvar_classification": "Likely benign",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "LB:1",
"phenotype_combined": "not provided",
"pathogenicity_classification_combined": "Likely benign",
"custom_annotations": null
}
],
"message": null
}