HTR2A 5-hydroxytryptamine receptor 2A
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 18 |
Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
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0 |
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0 |
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2 |
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42 |
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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
[No Data.]
Locus Zoom
Variants
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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 |
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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 |
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MGeND data only
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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 | 5-HT2A |
SYNONYM | HTR2 |
MIM | 182135 OMIM |
HGNC | HGNC:5293 HGNC |
Ensembl | ENSG00000102468 Ensembl |
AllianceGenome | HGNC:5293 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000542664.4 | hg38 | chr13 | 46,831,546 | 46,897,053 | 65,508 |
ENST00000543956.5 | hg38 | chr13 | 46,831,555 | 46,897,076 | 65,522 |
ENST00000542664.4 | hg19 | chr13 | 47,405,681 | 47,471,188 | 65,508 |
ENST00000543956.5 | hg19 | chr13 | 47,405,690 | 47,471,211 | 65,522 |
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