TXNDC17 thioredoxin domain containing 17
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Uncertain significance | 0 | 10 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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14 |
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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 |
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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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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 | TRP14 |
SYNONYM | TXNL5 |
MIM | 616967 OMIM |
HGNC | HGNC:28218 HGNC |
Ensembl | ENSG00000129235 Ensembl |
AllianceGenome | HGNC:28218 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000570330.5 | hg38 | chr17 | 6,641,016 | 6,643,114 | 2,099 |
ENST00000574838.1 | hg38 | chr17 | 6,641,043 | 6,643,429 | 2,387 |
ENST00000250101.10 | hg38 | chr17 | 6,641,060 | 6,644,541 | 3,482 |
ENST00000570330.5 | hg19 | chr17 | 6,544,336 | 6,546,434 | 2,099 |
ENST00000574838.1 | hg19 | chr17 | 6,544,363 | 6,546,749 | 2,387 |
ENST00000250101.10 | hg19 | chr17 | 6,544,380 | 6,547,861 | 3,482 |
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