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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: 22-39313303-A-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=22&pos=39313303&ref=A&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "22",
"pos": 39313303,
"ref": "A",
"alt": "G",
"effect": "missense_variant",
"transcript": "NM_000967.4",
"consequences": [
{
"aa_ref": "L",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL3",
"gene_hgnc_id": 10332,
"hgvs_c": "c.1055T>C",
"hgvs_p": "p.Leu352Pro",
"transcript": "NM_000967.4",
"protein_id": "NP_000958.1",
"transcript_support_level": null,
"aa_start": 352,
"aa_end": null,
"aa_length": 403,
"cds_start": 1055,
"cds_end": null,
"cds_length": 1212,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000216146.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_000967.4"
},
{
"aa_ref": "L",
"aa_alt": "P",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL3",
"gene_hgnc_id": 10332,
"hgvs_c": "c.1055T>C",
"hgvs_p": "p.Leu352Pro",
"transcript": "ENST00000216146.9",
"protein_id": "ENSP00000346001.3",
"transcript_support_level": 1,
"aa_start": 352,
"aa_end": null,
"aa_length": 403,
"cds_start": 1055,
"cds_end": null,
"cds_length": 1212,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_000967.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000216146.9"
},
{
"aa_ref": "L",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL3",
"gene_hgnc_id": 10332,
"hgvs_c": "c.899T>C",
"hgvs_p": "p.Leu300Pro",
"transcript": "ENST00000401609.5",
"protein_id": "ENSP00000386101.1",
"transcript_support_level": 1,
"aa_start": 300,
"aa_end": null,
"aa_length": 351,
"cds_start": 899,
"cds_end": null,
"cds_length": 1056,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000401609.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL3",
"gene_hgnc_id": 10332,
"hgvs_c": "n.1895T>C",
"hgvs_p": null,
"transcript": "ENST00000465618.5",
"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": "ENST00000465618.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"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": "RPL3",
"gene_hgnc_id": 10332,
"hgvs_c": "n.1186T>C",
"hgvs_p": null,
"transcript": "ENST00000467105.1",
"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": "ENST00000467105.1"
},
{
"aa_ref": "L",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL3",
"gene_hgnc_id": 10332,
"hgvs_c": "c.1133T>C",
"hgvs_p": "p.Leu378Pro",
"transcript": "ENST00000926233.1",
"protein_id": "ENSP00000596292.1",
"transcript_support_level": null,
"aa_start": 378,
"aa_end": null,
"aa_length": 429,
"cds_start": 1133,
"cds_end": null,
"cds_length": 1290,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000926233.1"
},
{
"aa_ref": "L",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL3",
"gene_hgnc_id": 10332,
"hgvs_c": "c.1076T>C",
"hgvs_p": "p.Leu359Pro",
"transcript": "ENST00000926234.1",
"protein_id": "ENSP00000596293.1",
"transcript_support_level": null,
"aa_start": 359,
"aa_end": null,
"aa_length": 410,
"cds_start": 1076,
"cds_end": null,
"cds_length": 1233,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000926234.1"
},
{
"aa_ref": "L",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL3",
"gene_hgnc_id": 10332,
"hgvs_c": "c.1064T>C",
"hgvs_p": "p.Leu355Pro",
"transcript": "ENST00000871470.1",
"protein_id": "ENSP00000541529.1",
"transcript_support_level": null,
"aa_start": 355,
"aa_end": null,
"aa_length": 406,
"cds_start": 1064,
"cds_end": null,
"cds_length": 1221,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000871470.1"
},
{
"aa_ref": "L",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL3",
"gene_hgnc_id": 10332,
"hgvs_c": "c.1046T>C",
"hgvs_p": "p.Leu349Pro",
"transcript": "ENST00000871474.1",
"protein_id": "ENSP00000541533.1",
"transcript_support_level": null,
"aa_start": 349,
"aa_end": null,
"aa_length": 400,
"cds_start": 1046,
"cds_end": null,
"cds_length": 1203,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000871474.1"
},
{
"aa_ref": "L",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL3",
"gene_hgnc_id": 10332,
"hgvs_c": "c.1055T>C",
"hgvs_p": "p.Leu352Pro",
"transcript": "ENST00000871477.1",
"protein_id": "ENSP00000541536.1",
"transcript_support_level": null,
"aa_start": 352,
"aa_end": null,
"aa_length": 399,
"cds_start": 1055,
"cds_end": null,
"cds_length": 1200,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000871477.1"
},
{
"aa_ref": "L",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL3",
"gene_hgnc_id": 10332,
"hgvs_c": "c.1037T>C",
"hgvs_p": "p.Leu346Pro",
"transcript": "ENST00000926227.1",
"protein_id": "ENSP00000596286.1",
"transcript_support_level": null,
"aa_start": 346,
"aa_end": null,
"aa_length": 397,
"cds_start": 1037,
"cds_end": null,
"cds_length": 1194,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000926227.1"
},
{
"aa_ref": "L",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL3",
"gene_hgnc_id": 10332,
"hgvs_c": "c.1031T>C",
"hgvs_p": "p.Leu344Pro",
"transcript": "ENST00000871471.1",
"protein_id": "ENSP00000541530.1",
"transcript_support_level": null,
"aa_start": 344,
"aa_end": null,
"aa_length": 395,
"cds_start": 1031,
"cds_end": null,
"cds_length": 1188,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000871471.1"
},
{
"aa_ref": "L",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL3",
"gene_hgnc_id": 10332,
"hgvs_c": "c.1028T>C",
"hgvs_p": "p.Leu343Pro",
"transcript": "ENST00000871469.1",
"protein_id": "ENSP00000541528.1",
"transcript_support_level": null,
"aa_start": 343,
"aa_end": null,
"aa_length": 394,
"cds_start": 1028,
"cds_end": null,
"cds_length": 1185,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000871469.1"
},
{
"aa_ref": "L",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL3",
"gene_hgnc_id": 10332,
"hgvs_c": "c.1013T>C",
"hgvs_p": "p.Leu338Pro",
"transcript": "ENST00000926230.1",
"protein_id": "ENSP00000596289.1",
"transcript_support_level": null,
"aa_start": 338,
"aa_end": null,
"aa_length": 389,
"cds_start": 1013,
"cds_end": null,
"cds_length": 1170,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000926230.1"
},
{
"aa_ref": "L",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL3",
"gene_hgnc_id": 10332,
"hgvs_c": "c.1010T>C",
"hgvs_p": "p.Leu337Pro",
"transcript": "ENST00000871473.1",
"protein_id": "ENSP00000541532.1",
"transcript_support_level": null,
"aa_start": 337,
"aa_end": null,
"aa_length": 388,
"cds_start": 1010,
"cds_end": null,
"cds_length": 1167,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000871473.1"
},
{
"aa_ref": "L",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL3",
"gene_hgnc_id": 10332,
"hgvs_c": "c.959T>C",
"hgvs_p": "p.Leu320Pro",
"transcript": "ENST00000871468.1",
"protein_id": "ENSP00000541527.1",
"transcript_support_level": null,
"aa_start": 320,
"aa_end": null,
"aa_length": 371,
"cds_start": 959,
"cds_end": null,
"cds_length": 1116,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000871468.1"
},
{
"aa_ref": "L",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL3",
"gene_hgnc_id": 10332,
"hgvs_c": "c.953T>C",
"hgvs_p": "p.Leu318Pro",
"transcript": "ENST00000871472.1",
"protein_id": "ENSP00000541531.1",
"transcript_support_level": null,
"aa_start": 318,
"aa_end": null,
"aa_length": 369,
"cds_start": 953,
"cds_end": null,
"cds_length": 1110,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000871472.1"
},
{
"aa_ref": "L",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL3",
"gene_hgnc_id": 10332,
"hgvs_c": "c.917T>C",
"hgvs_p": "p.Leu306Pro",
"transcript": "ENST00000926229.1",
"protein_id": "ENSP00000596288.1",
"transcript_support_level": null,
"aa_start": 306,
"aa_end": null,
"aa_length": 357,
"cds_start": 917,
"cds_end": null,
"cds_length": 1074,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000926229.1"
},
{
"aa_ref": "L",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL3",
"gene_hgnc_id": 10332,
"hgvs_c": "c.908T>C",
"hgvs_p": "p.Leu303Pro",
"transcript": "NM_001033853.2",
"protein_id": "NP_001029025.1",
"transcript_support_level": null,
"aa_start": 303,
"aa_end": null,
"aa_length": 354,
"cds_start": 908,
"cds_end": null,
"cds_length": 1065,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001033853.2"
},
{
"aa_ref": "L",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL3",
"gene_hgnc_id": 10332,
"hgvs_c": "c.896T>C",
"hgvs_p": "p.Leu299Pro",
"transcript": "ENST00000871475.1",
"protein_id": "ENSP00000541534.1",
"transcript_support_level": null,
"aa_start": 299,
"aa_end": null,
"aa_length": 350,
"cds_start": 896,
"cds_end": null,
"cds_length": 1053,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000871475.1"
},
{
"aa_ref": "L",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL3",
"gene_hgnc_id": 10332,
"hgvs_c": "c.803T>C",
"hgvs_p": "p.Leu268Pro",
"transcript": "ENST00000926235.1",
"protein_id": "ENSP00000596294.1",
"transcript_support_level": null,
"aa_start": 268,
"aa_end": null,
"aa_length": 319,
"cds_start": 803,
"cds_end": null,
"cds_length": 960,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000926235.1"
},
{
"aa_ref": "L",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "RPL3",
"gene_hgnc_id": 10332,
"hgvs_c": "c.605T>C",
"hgvs_p": "p.Leu202Pro",
"transcript": "ENST00000926236.1",
"protein_id": "ENSP00000596295.1",
"transcript_support_level": null,
"aa_start": 202,
"aa_end": null,
"aa_length": 253,
"cds_start": 605,
"cds_end": null,
"cds_length": 762,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000926236.1"
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{
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"canonical": false,
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"consequences": [
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"intron_variant"
],
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},
{
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"intron_variant"
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"transcript": "ENST00000871476.1",
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"biotype": "protein_coding",
"feature": "ENST00000871476.1"
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
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"intron_variant"
],
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"transcript": "ENST00000926232.1",
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"biotype": "protein_coding",
"feature": "ENST00000926232.1"
},
{
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"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
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"gene_symbol": "RPL3",
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"transcript": "ENST00000926228.1",
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"biotype": "protein_coding",
"feature": "ENST00000926228.1"
},
{
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"protein_coding": true,
"strand": false,
"consequences": [
"splice_region_variant",
"intron_variant"
],
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"transcript": "ENST00000926231.1",
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"biotype": "protein_coding",
"feature": "ENST00000926231.1"
},
{
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"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
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"gene_symbol": "RPL3",
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"transcript": "ENST00000464182.5",
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"biotype": "retained_intron",
"feature": "ENST00000464182.5"
},
{
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"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
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"exon_count": 2,
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"gene_symbol": "RPL3",
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"hgvs_c": "n.104T>C",
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"transcript": "ENST00000473638.5",
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"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": "ENST00000473638.5"
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],
"gene_symbol": "RPL3",
"gene_hgnc_id": 10332,
"dbsnp": "rs758783912",
"frequency_reference_population": null,
"hom_count_reference_population": 0,
"allele_count_reference_population": 0,
"gnomad_exomes_af": 0.00000205246,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 3,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.8161430358886719,
"computational_prediction_selected": "Pathogenic",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.706,
"revel_prediction": "Pathogenic",
"alphamissense_score": 0.99,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.21,
"bayesdelnoaf_prediction": "Pathogenic",
"phylop100way_score": 9.32,
"phylop100way_prediction": "Pathogenic",
"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": 3,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,PP3",
"acmg_by_gene": [
{
"score": 3,
"benign_score": 0,
"pathogenic_score": 3,
"criteria": [
"PM2",
"PP3"
],
"verdict": "Uncertain_significance",
"transcript": "NM_000967.4",
"gene_symbol": "RPL3",
"hgnc_id": 10332,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.1055T>C",
"hgvs_p": "p.Leu352Pro"
}
],
"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
}