HTR3D 5-hydroxytryptamine receptor 3D
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely pathogenic | 1 | 0 |
Likely benign | 0 | 18 |
Uncertain significance | 0 | 66 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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84 |
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0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | 5HT3D |
MIM | 610122 OMIM |
HGNC | HGNC:24004 HGNC |
Ensembl | ENSG00000186090 Ensembl |
AllianceGenome | HGNC:24004 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000334128.6 | hg38 | chr3 | 184,031,544 | 184,039,369 | 7,826 |
ENST00000453435.1 | hg38 | chr3 | 184,035,104 | 184,039,200 | 4,097 |
ENST00000382489.3 | hg38 | chr3 | 184,032,831 | 184,039,284 | 6,454 |
ENST00000428798.7 | hg38 | chr3 | 184,031,742 | 184,039,369 | 7,628 |
ENST00000334128.6 | hg19 | chr3 | 183,749,332 | 183,757,157 | 7,826 |
ENST00000428798.7 | hg19 | chr3 | 183,749,530 | 183,757,157 | 7,628 |
ENST00000382489.3 | hg19 | chr3 | 183,750,619 | 183,757,072 | 6,454 |
ENST00000453435.1 | hg19 | chr3 | 183,752,892 | 183,756,988 | 4,097 |
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