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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: 21-32603205-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=21&pos=32603205&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "21",
"pos": 32603205,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_001350338.2",
"consequences": [
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP298",
"gene_hgnc_id": 1301,
"hgvs_c": "c.622G>A",
"hgvs_p": "p.Val208Met",
"transcript": "NM_021254.4",
"protein_id": "NP_067077.1",
"transcript_support_level": null,
"aa_start": 208,
"aa_end": null,
"aa_length": 290,
"cds_start": 622,
"cds_end": null,
"cds_length": 873,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000290155.8",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_021254.4"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP298",
"gene_hgnc_id": 1301,
"hgvs_c": "c.622G>A",
"hgvs_p": "p.Val208Met",
"transcript": "ENST00000290155.8",
"protein_id": "ENSP00000290155.3",
"transcript_support_level": 1,
"aa_start": 208,
"aa_end": null,
"aa_length": 290,
"cds_start": 622,
"cds_end": null,
"cds_length": 873,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_021254.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000290155.8"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP298-TCP10L",
"gene_hgnc_id": 54636,
"hgvs_c": "c.622G>A",
"hgvs_p": "p.Val208Met",
"transcript": "ENST00000673807.1",
"protein_id": "ENSP00000501088.1",
"transcript_support_level": null,
"aa_start": 208,
"aa_end": null,
"aa_length": 389,
"cds_start": 622,
"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": "ENST00000673807.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP298",
"gene_hgnc_id": 1301,
"hgvs_c": "c.622G>A",
"hgvs_p": "p.Val208Met",
"transcript": "ENST00000382549.8",
"protein_id": "ENSP00000371989.4",
"transcript_support_level": 1,
"aa_start": 208,
"aa_end": null,
"aa_length": 245,
"cds_start": 622,
"cds_end": null,
"cds_length": 738,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000382549.8"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP298-TCP10L",
"gene_hgnc_id": 54636,
"hgvs_c": "c.622G>A",
"hgvs_p": "p.Val208Met",
"transcript": "NM_001350338.2",
"protein_id": "NP_001337267.1",
"transcript_support_level": null,
"aa_start": 208,
"aa_end": null,
"aa_length": 389,
"cds_start": 622,
"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": "NM_001350338.2"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP298-TCP10L",
"gene_hgnc_id": 54636,
"hgvs_c": "c.622G>A",
"hgvs_p": "p.Val208Met",
"transcript": "ENST00000673985.1",
"protein_id": "ENSP00000500984.1",
"transcript_support_level": null,
"aa_start": 208,
"aa_end": null,
"aa_length": 373,
"cds_start": 622,
"cds_end": null,
"cds_length": 1122,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000673985.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP298",
"gene_hgnc_id": 1301,
"hgvs_c": "c.718G>A",
"hgvs_p": "p.Val240Met",
"transcript": "ENST00000877680.1",
"protein_id": "ENSP00000547739.1",
"transcript_support_level": null,
"aa_start": 240,
"aa_end": null,
"aa_length": 322,
"cds_start": 718,
"cds_end": null,
"cds_length": 969,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000877680.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP298",
"gene_hgnc_id": 1301,
"hgvs_c": "c.715G>A",
"hgvs_p": "p.Val239Met",
"transcript": "ENST00000926992.1",
"protein_id": "ENSP00000597051.1",
"transcript_support_level": null,
"aa_start": 239,
"aa_end": null,
"aa_length": 321,
"cds_start": 715,
"cds_end": null,
"cds_length": 966,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000926992.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP298",
"gene_hgnc_id": 1301,
"hgvs_c": "c.709G>A",
"hgvs_p": "p.Val237Met",
"transcript": "ENST00000877679.1",
"protein_id": "ENSP00000547738.1",
"transcript_support_level": null,
"aa_start": 237,
"aa_end": null,
"aa_length": 319,
"cds_start": 709,
"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": "ENST00000877679.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP298-TCP10L",
"gene_hgnc_id": 54636,
"hgvs_c": "c.622G>A",
"hgvs_p": "p.Val208Met",
"transcript": "ENST00000673945.1",
"protein_id": "ENSP00000501020.1",
"transcript_support_level": null,
"aa_start": 208,
"aa_end": null,
"aa_length": 317,
"cds_start": 622,
"cds_end": null,
"cds_length": 954,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000673945.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP298",
"gene_hgnc_id": 1301,
"hgvs_c": "c.673G>A",
"hgvs_p": "p.Val225Met",
"transcript": "ENST00000926995.1",
"protein_id": "ENSP00000597054.1",
"transcript_support_level": null,
"aa_start": 225,
"aa_end": null,
"aa_length": 307,
"cds_start": 673,
"cds_end": null,
"cds_length": 924,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000926995.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP298",
"gene_hgnc_id": 1301,
"hgvs_c": "c.658G>A",
"hgvs_p": "p.Val220Met",
"transcript": "ENST00000926993.1",
"protein_id": "ENSP00000597052.1",
"transcript_support_level": null,
"aa_start": 220,
"aa_end": null,
"aa_length": 302,
"cds_start": 658,
"cds_end": null,
"cds_length": 909,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000926993.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP298-TCP10L",
"gene_hgnc_id": 54636,
"hgvs_c": "c.523G>A",
"hgvs_p": "p.Val175Met",
"transcript": "ENST00000431216.5",
"protein_id": "ENSP00000391771.1",
"transcript_support_level": 5,
"aa_start": 175,
"aa_end": null,
"aa_length": 295,
"cds_start": 523,
"cds_end": null,
"cds_length": 889,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000431216.5"
},
{
"aa_ref": "V",
"aa_alt": "M",
"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": "CFAP298",
"gene_hgnc_id": 1301,
"hgvs_c": "c.718G>A",
"hgvs_p": "p.Val240Met",
"transcript": "ENST00000926989.1",
"protein_id": "ENSP00000597048.1",
"transcript_support_level": null,
"aa_start": 240,
"aa_end": null,
"aa_length": 290,
"cds_start": 718,
"cds_end": null,
"cds_length": 873,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000926989.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP298",
"gene_hgnc_id": 1301,
"hgvs_c": "c.622G>A",
"hgvs_p": "p.Val208Met",
"transcript": "ENST00000926990.1",
"protein_id": "ENSP00000597049.1",
"transcript_support_level": null,
"aa_start": 208,
"aa_end": null,
"aa_length": 287,
"cds_start": 622,
"cds_end": null,
"cds_length": 864,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000926990.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP298",
"gene_hgnc_id": 1301,
"hgvs_c": "c.622G>A",
"hgvs_p": "p.Val208Met",
"transcript": "NM_001350337.2",
"protein_id": "NP_001337266.1",
"transcript_support_level": null,
"aa_start": 208,
"aa_end": null,
"aa_length": 269,
"cds_start": 622,
"cds_end": null,
"cds_length": 810,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001350337.2"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP298",
"gene_hgnc_id": 1301,
"hgvs_c": "c.622G>A",
"hgvs_p": "p.Val208Met",
"transcript": "NM_001350336.2",
"protein_id": "NP_001337265.1",
"transcript_support_level": null,
"aa_start": 208,
"aa_end": null,
"aa_length": 258,
"cds_start": 622,
"cds_end": null,
"cds_length": 777,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001350336.2"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP298",
"gene_hgnc_id": 1301,
"hgvs_c": "c.622G>A",
"hgvs_p": "p.Val208Met",
"transcript": "ENST00000440966.5",
"protein_id": "ENSP00000411467.1",
"transcript_support_level": 3,
"aa_start": 208,
"aa_end": null,
"aa_length": 258,
"cds_start": 622,
"cds_end": null,
"cds_length": 777,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000440966.5"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP298-TCP10L",
"gene_hgnc_id": 54636,
"hgvs_c": "c.334G>A",
"hgvs_p": "p.Val112Met",
"transcript": "ENST00000553001.2",
"protein_id": "ENSP00000446874.2",
"transcript_support_level": 5,
"aa_start": 112,
"aa_end": null,
"aa_length": 252,
"cds_start": 334,
"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": "ENST00000553001.2"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP298",
"gene_hgnc_id": 1301,
"hgvs_c": "c.622G>A",
"hgvs_p": "p.Val208Met",
"transcript": "NM_001350335.2",
"protein_id": "NP_001337264.1",
"transcript_support_level": null,
"aa_start": 208,
"aa_end": null,
"aa_length": 245,
"cds_start": 622,
"cds_end": null,
"cds_length": 738,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001350335.2"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP298",
"gene_hgnc_id": 1301,
"hgvs_c": "c.454G>A",
"hgvs_p": "p.Val152Met",
"transcript": "ENST00000877678.1",
"protein_id": "ENSP00000547737.1",
"transcript_support_level": null,
"aa_start": 152,
"aa_end": null,
"aa_length": 234,
"cds_start": 454,
"cds_end": null,
"cds_length": 705,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000877678.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP298",
"gene_hgnc_id": 1301,
"hgvs_c": "c.454G>A",
"hgvs_p": "p.Val152Met",
"transcript": "ENST00000926994.1",
"protein_id": "ENSP00000597053.1",
"transcript_support_level": null,
"aa_start": 152,
"aa_end": null,
"aa_length": 202,
"cds_start": 454,
"cds_end": null,
"cds_length": 609,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
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"biotype": "nonsense_mediated_decay",
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},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
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],
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"exon_count": 12,
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"transcript": "ENST00000674122.1",
"protein_id": "ENSP00000501276.1",
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"feature": "ENST00000674122.1"
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 5,
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"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP298-TCP10L",
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"hgvs_c": "n.622G>A",
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"transcript": "ENST00000674123.1",
"protein_id": "ENSP00000501038.1",
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"aa_start": null,
"aa_end": null,
"aa_length": null,
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"cdna_start": null,
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"biotype": "nonsense_mediated_decay",
"feature": "ENST00000674123.1"
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 5,
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"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP298-TCP10L",
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"hgvs_c": "n.756G>A",
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"transcript": "NR_146638.2",
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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": "pseudogene",
"feature": "NR_146638.2"
},
{
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"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
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"exon_count": 12,
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"gene_symbol": "CFAP298-TCP10L",
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"biotype": "pseudogene",
"feature": "NR_146639.2"
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 4,
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"exon_count": 6,
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"gene_symbol": "CFAP298",
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"hgvs_c": "n.*137G>A",
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"transcript": "ENST00000300260.7",
"protein_id": "ENSP00000300260.7",
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"biotype": "nonsense_mediated_decay",
"feature": "ENST00000300260.7"
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
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"exon_count": 5,
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"gene_symbol": "CFAP298",
"gene_hgnc_id": 1301,
"hgvs_c": "c.*20G>A",
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"transcript": "ENST00000458138.1",
"protein_id": "ENSP00000393104.1",
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"cdna_start": null,
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"cdna_length": null,
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"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000458138.1"
}
],
"gene_symbol": "CFAP298-TCP10L",
"gene_hgnc_id": 54636,
"dbsnp": "rs61735781",
"frequency_reference_population": 0.005904429,
"hom_count_reference_population": 55,
"allele_count_reference_population": 9531,
"gnomad_exomes_af": 0.0060656,
"gnomad_genomes_af": 0.00435804,
"gnomad_exomes_ac": 8867,
"gnomad_genomes_ac": 664,
"gnomad_exomes_homalt": 53,
"gnomad_genomes_homalt": 2,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.009092539548873901,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.009999999776482582,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.162,
"revel_prediction": "Benign",
"alphamissense_score": 0.5653,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.15,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 2.568,
"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": -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": "NM_001350338.2",
"gene_symbol": "CFAP298-TCP10L",
"hgnc_id": 54636,
"effects": [
"missense_variant"
],
"inheritance_mode": "",
"hgvs_c": "c.622G>A",
"hgvs_p": "p.Val208Met"
},
{
"score": -20,
"benign_score": 20,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong",
"BS1",
"BS2"
],
"verdict": "Benign",
"transcript": "NM_021254.4",
"gene_symbol": "CFAP298",
"hgnc_id": 1301,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD,AR",
"hgvs_c": "c.622G>A",
"hgvs_p": "p.Val208Met"
}
],
"clinvar_disease": "not provided",
"clinvar_classification": "Benign/Likely benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "LB:3 B:1",
"phenotype_combined": "not provided",
"pathogenicity_classification_combined": "Benign/Likely benign",
"custom_annotations": null
}
],
"message": null
}