TST thiosulfate sulfurtransferase
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 8 | 0 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 48 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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52 |
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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 | : | |
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 | RDS |
MIM | 180370 OMIM |
HGNC | HGNC:12388 HGNC |
Ensembl | ENSG00000128311 Ensembl |
AllianceGenome | HGNC:12388 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000403892.7 | hg38 | chr22 | 37,010,859 | 37,019,467 | 8,609 |
ENST00000249042.8 | hg38 | chr22 | 37,010,865 | 37,019,447 | 8,583 |
ENST00000622841.1 | hg38 | chr22 | 37,010,859 | 37,020,183 | 9,325 |
ENST00000403892.7 | hg19 | chr22 | 37,406,900 | 37,415,508 | 8,609 |
ENST00000622841.1 | hg19 | chr22 | 37,406,900 | 37,416,224 | 9,325 |
ENST00000249042.8 | hg19 | chr22 | 37,406,906 | 37,415,488 | 8,583 |
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