TSTD1 thiosulfate sulfurtransferase like domain containing 1
Information
- Symbol
- TSTD1
- Type
- protein-coding
- Description
- thiosulfate sulfurtransferase like domain containing 1
- Entrez Gene ID
- 100131187
- Genome
- hg19
- Position
- chr1:161,007,421-161,008,754
- Genome
- hg38
- Position
- chr1:161,037,631-161,038,964
- MIM
- 616041 OMIM
- HGNC
- HGNC:35410 HGNC
- Ensembl
- ENSG00000215845 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 22 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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22 |
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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
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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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 |
---|---|
SYNONYM | KAT |
SYNONYM | TST |
MIM | 616041 OMIM |
HGNC | HGNC:35410 HGNC |
Ensembl | ENSG00000215845 Ensembl |
AllianceGenome | HGNC:35410 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000423014.3 | hg38 | chr1 | 161,037,631 | 161,038,964 | 1,334 |
ENST00000368023.7 | hg38 | chr1 | 161,037,631 | 161,038,950 | 1,320 |
ENST00000368024.5 | hg38 | chr1 | 161,037,631 | 161,038,977 | 1,347 |
ENST00000466967.1 | hg38 | chr1 | 161,037,692 | 161,038,729 | 1,038 |
ENST00000318289.14 | hg38 | chr1 | 161,037,631 | 161,038,937 | 1,307 |
ENST00000318289.14 | hg19 | chr1 | 161,007,421 | 161,008,727 | 1,307 |
ENST00000368023.7 | hg19 | chr1 | 161,007,421 | 161,008,740 | 1,320 |
ENST00000423014.3 | hg19 | chr1 | 161,007,421 | 161,008,754 | 1,334 |
ENST00000368024.5 | hg19 | chr1 | 161,007,421 | 161,008,767 | 1,347 |
ENST00000466967.1 | hg19 | chr1 | 161,007,482 | 161,008,519 | 1,038 |
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