TAS2R38 taste 2 receptor member 38
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 12 | 0 |
Likely benign | 0 | 4 |
drug response | 0 | 4 |
Uncertain significance | 0 | 42 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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46 |
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4 |
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 |
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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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Filtering | : |
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 | PTC |
SYNONYM | T2R38 |
SYNONYM | T2R61 |
SYNONYM | THIOT |
MIM | 607751 OMIM |
HGNC | HGNC:9584 HGNC |
Ensembl | ENSG00000257138 Ensembl |
AllianceGenome | HGNC:9584 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000547270.1 | hg38 | chr7 | 141,972,631 | 141,973,773 | 1,143 |
ENST00000547270.1 | hg19 | chr7 | 141,672,431 | 141,673,573 | 1,143 |
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