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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: 17-82249433-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=82249433&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "17",
"pos": 82249433,
"ref": "G",
"alt": "A",
"effect": "missense_variant,splice_region_variant",
"transcript": "NM_001363749.2",
"consequences": [
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CSNK1D",
"gene_hgnc_id": 2452,
"hgvs_c": "c.1055C>T",
"hgvs_p": "p.Thr352Met",
"transcript": "NM_001893.6",
"protein_id": "NP_001884.2",
"transcript_support_level": null,
"aa_start": 352,
"aa_end": null,
"aa_length": 415,
"cds_start": 1055,
"cds_end": null,
"cds_length": 1248,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000314028.11",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001893.6"
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CSNK1D",
"gene_hgnc_id": 2452,
"hgvs_c": "c.1055C>T",
"hgvs_p": "p.Thr352Met",
"transcript": "ENST00000314028.11",
"protein_id": "ENSP00000324464.6",
"transcript_support_level": 1,
"aa_start": 352,
"aa_end": null,
"aa_length": 415,
"cds_start": 1055,
"cds_end": null,
"cds_length": 1248,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001893.6",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000314028.11"
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CSNK1D",
"gene_hgnc_id": 2452,
"hgvs_c": "c.1055C>T",
"hgvs_p": "p.Thr352Met",
"transcript": "ENST00000392334.7",
"protein_id": "ENSP00000376146.2",
"transcript_support_level": 1,
"aa_start": 352,
"aa_end": null,
"aa_length": 409,
"cds_start": 1055,
"cds_end": null,
"cds_length": 1230,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000392334.7"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"splice_region_variant",
"non_coding_transcript_exon_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CSNK1D",
"gene_hgnc_id": 2452,
"hgvs_c": "n.*627C>T",
"hgvs_p": null,
"transcript": "ENST00000580784.5",
"protein_id": "ENSP00000463906.1",
"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": "ENST00000580784.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CSNK1D",
"gene_hgnc_id": 2452,
"hgvs_c": "n.*627C>T",
"hgvs_p": null,
"transcript": "ENST00000580784.5",
"protein_id": "ENSP00000463906.1",
"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": "ENST00000580784.5"
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CSNK1D",
"gene_hgnc_id": 2452,
"hgvs_c": "c.1055C>T",
"hgvs_p": "p.Thr352Met",
"transcript": "ENST00000865418.1",
"protein_id": "ENSP00000535477.1",
"transcript_support_level": null,
"aa_start": 352,
"aa_end": null,
"aa_length": 436,
"cds_start": 1055,
"cds_end": null,
"cds_length": 1311,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000865418.1"
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CSNK1D",
"gene_hgnc_id": 2452,
"hgvs_c": "c.1055C>T",
"hgvs_p": "p.Thr352Met",
"transcript": "NM_001363749.2",
"protein_id": "NP_001350678.1",
"transcript_support_level": null,
"aa_start": 352,
"aa_end": null,
"aa_length": 427,
"cds_start": 1055,
"cds_end": null,
"cds_length": 1284,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001363749.2"
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CSNK1D",
"gene_hgnc_id": 2452,
"hgvs_c": "c.1055C>T",
"hgvs_p": "p.Thr352Met",
"transcript": "ENST00000398519.9",
"protein_id": "ENSP00000381531.5",
"transcript_support_level": 5,
"aa_start": 352,
"aa_end": null,
"aa_length": 427,
"cds_start": 1055,
"cds_end": null,
"cds_length": 1284,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000398519.9"
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CSNK1D",
"gene_hgnc_id": 2452,
"hgvs_c": "c.1055C>T",
"hgvs_p": "p.Thr352Met",
"transcript": "NM_139062.4",
"protein_id": "NP_620693.1",
"transcript_support_level": null,
"aa_start": 352,
"aa_end": null,
"aa_length": 409,
"cds_start": 1055,
"cds_end": null,
"cds_length": 1230,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_139062.4"
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CSNK1D",
"gene_hgnc_id": 2452,
"hgvs_c": "c.1037C>T",
"hgvs_p": "p.Thr346Met",
"transcript": "ENST00000865420.1",
"protein_id": "ENSP00000535479.1",
"transcript_support_level": null,
"aa_start": 346,
"aa_end": null,
"aa_length": 409,
"cds_start": 1037,
"cds_end": null,
"cds_length": 1230,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000865420.1"
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CSNK1D",
"gene_hgnc_id": 2452,
"hgvs_c": "c.1055C>T",
"hgvs_p": "p.Thr352Met",
"transcript": "ENST00000865419.1",
"protein_id": "ENSP00000535478.1",
"transcript_support_level": null,
"aa_start": 352,
"aa_end": null,
"aa_length": 384,
"cds_start": 1055,
"cds_end": null,
"cds_length": 1155,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000865419.1"
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CSNK1D",
"gene_hgnc_id": 2452,
"hgvs_c": "c.1055C>T",
"hgvs_p": "p.Thr352Met",
"transcript": "XM_005256336.5",
"protein_id": "XP_005256393.1",
"transcript_support_level": null,
"aa_start": 352,
"aa_end": null,
"aa_length": 450,
"cds_start": 1055,
"cds_end": null,
"cds_length": 1353,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_005256336.5"
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CSNK1D",
"gene_hgnc_id": 2452,
"hgvs_c": "c.1055C>T",
"hgvs_p": "p.Thr352Met",
"transcript": "XM_047435379.1",
"protein_id": "XP_047291335.1",
"transcript_support_level": null,
"aa_start": 352,
"aa_end": null,
"aa_length": 432,
"cds_start": 1055,
"cds_end": null,
"cds_length": 1299,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047435379.1"
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CSNK1D",
"gene_hgnc_id": 2452,
"hgvs_c": "c.1055C>T",
"hgvs_p": "p.Thr352Met",
"transcript": "XM_047435380.1",
"protein_id": "XP_047291336.1",
"transcript_support_level": null,
"aa_start": 352,
"aa_end": null,
"aa_length": 400,
"cds_start": 1055,
"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": "XM_047435380.1"
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CSNK1D",
"gene_hgnc_id": 2452,
"hgvs_c": "c.884C>T",
"hgvs_p": "p.Thr295Met",
"transcript": "XM_047435381.1",
"protein_id": "XP_047291337.1",
"transcript_support_level": null,
"aa_start": 295,
"aa_end": null,
"aa_length": 393,
"cds_start": 884,
"cds_end": null,
"cds_length": 1182,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047435381.1"
},
{
"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": 2,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "SLC16A3",
"gene_hgnc_id": 10924,
"hgvs_c": "c.725-11466G>A",
"hgvs_p": null,
"transcript": "ENST00000583025.1",
"protein_id": "ENSP00000463005.1",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": 306,
"cds_start": null,
"cds_end": null,
"cds_length": 921,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000583025.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"splice_region_variant",
"non_coding_transcript_exon_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CSNK1D",
"gene_hgnc_id": 2452,
"hgvs_c": "n.*369C>T",
"hgvs_p": null,
"transcript": "ENST00000269361.11",
"protein_id": "ENSP00000269361.7",
"transcript_support_level": 5,
"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": "ENST00000269361.11"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"splice_region_variant",
"non_coding_transcript_exon_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CSNK1D",
"gene_hgnc_id": 2452,
"hgvs_c": "n.*445C>T",
"hgvs_p": null,
"transcript": "ENST00000403276.7",
"protein_id": "ENSP00000385769.3",
"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": "ENST00000403276.7"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CSNK1D",
"gene_hgnc_id": 2452,
"hgvs_c": "n.64C>T",
"hgvs_p": null,
"transcript": "ENST00000578501.5",
"protein_id": null,
"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": "retained_intron",
"feature": "ENST00000578501.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"splice_region_variant",
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CSNK1D",
"gene_hgnc_id": 2452,
"hgvs_c": "n.308C>T",
"hgvs_p": null,
"transcript": "ENST00000580565.1",
"protein_id": null,
"transcript_support_level": 4,
"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": "ENST00000580565.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CSNK1D",
"gene_hgnc_id": 2452,
"hgvs_c": "n.413C>T",
"hgvs_p": null,
"transcript": "ENST00000581108.5",
"protein_id": null,
"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": "retained_intron",
"feature": "ENST00000581108.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"splice_region_variant",
"non_coding_transcript_exon_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CSNK1D",
"gene_hgnc_id": 2452,
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{
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"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
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"non_coding_transcript_exon_variant"
],
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"gene_symbol": "CSNK1D",
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"biotype": "retained_intron",
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},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
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],
"exon_rank": 1,
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"exon_count": 1,
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"gene_symbol": "ENSG00000280407",
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"biotype": "TEC",
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},
{
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"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"splice_region_variant",
"non_coding_transcript_exon_variant"
],
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"gene_symbol": "CSNK1D",
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"biotype": "pseudogene",
"feature": "NR_110578.2"
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
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"biotype": "nonsense_mediated_decay",
"feature": "ENST00000269361.11"
},
{
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"protein_coding": false,
"strand": false,
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"3_prime_UTR_variant"
],
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"exon_count": 8,
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"gene_symbol": "CSNK1D",
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"hgvs_c": "n.*445C>T",
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"transcript": "ENST00000403276.7",
"protein_id": "ENSP00000385769.3",
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"biotype": "nonsense_mediated_decay",
"feature": "ENST00000403276.7"
},
{
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"canonical": false,
"protein_coding": false,
"strand": false,
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"3_prime_UTR_variant"
],
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"gene_symbol": "CSNK1D",
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"biotype": "nonsense_mediated_decay",
"feature": "ENST00000581241.6"
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
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"exon_count": 5,
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"gene_symbol": "CSNK1D",
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"transcript": "ENST00000578904.1",
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"biotype": "pseudogene",
"feature": "ENST00000578904.1"
},
{
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"protein_coding": false,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
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"exon_count": 7,
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"gene_symbol": "CSNK1D",
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"transcript": "ENST00000582844.5",
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"biotype": "pseudogene",
"feature": "ENST00000582844.5"
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{
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"strand": true,
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"downstream_gene_variant"
],
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"exon_count": 8,
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"gene_symbol": "CSNK1D",
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"hgvs_c": "n.*90C>T",
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"transcript": "XR_007065265.1",
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"biotype": "pseudogene",
"feature": "XR_007065265.1"
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],
"gene_symbol": "CSNK1D",
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"dbsnp": "rs768280334",
"frequency_reference_population": 0.00006646042,
"hom_count_reference_population": 0,
"allele_count_reference_population": 102,
"gnomad_exomes_af": 0.0000716053,
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"gnomad_exomes_ac": 99,
"gnomad_genomes_ac": 3,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.33379098773002625,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.6779999732971191,
"splice_prediction_selected": "Benign",
"splice_source_selected": "dbscSNV1_RF",
"revel_score": 0.194,
"revel_prediction": "Benign",
"alphamissense_score": 0.0984,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.24,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 9.304,
"phylop100way_prediction": "Pathogenic",
"spliceai_max_score": 0,
"spliceai_max_prediction": "Benign",
"dbscsnv_ada_score": 0.998657609076464,
"dbscsnv_ada_prediction": "Pathogenic",
"apogee2_score": null,
"apogee2_prediction": null,
"mitotip_score": null,
"mitotip_prediction": null,
"acmg_score": -5,
"acmg_classification": "Likely_benign",
"acmg_criteria": "BP4,BS2",
"acmg_by_gene": [
{
"score": -5,
"benign_score": 5,
"pathogenic_score": 0,
"criteria": [
"BP4",
"BS2"
],
"verdict": "Likely_benign",
"transcript": "NM_001363749.2",
"gene_symbol": "CSNK1D",
"hgnc_id": 2452,
"effects": [
"missense_variant",
"splice_region_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.1055C>T",
"hgvs_p": "p.Thr352Met"
},
{
"score": 1,
"benign_score": 1,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000583025.1",
"gene_symbol": "SLC16A3",
"hgnc_id": 10924,
"effects": [
"intron_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.725-11466G>A",
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},
{
"score": 1,
"benign_score": 1,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000624920.1",
"gene_symbol": "ENSG00000280407",
"hgnc_id": null,
"effects": [
"non_coding_transcript_exon_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.367G>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
}