TXNDC2 thioredoxin domain containing 2
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 36 |
Uncertain significance | 0 | 56 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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96 |
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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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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 | SPTRX |
SYNONYM | SPTRX1 |
MIM | 617790 OMIM |
HGNC | HGNC:16470 HGNC |
Ensembl | ENSG00000168454 Ensembl |
AllianceGenome | HGNC:16470 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000306084.6 | hg38 | chr18 | 9,885,976 | 9,888,153 | 2,178 |
ENST00000357775.6 | hg38 | chr18 | 9,885,973 | 9,889,275 | 3,303 |
ENST00000536353.2 | hg38 | chr18 | 9,885,766 | 9,888,380 | 2,615 |
ENST00000536353.2 | hg19 | chr18 | 9,885,763 | 9,888,377 | 2,615 |
ENST00000357775.6 | hg19 | chr18 | 9,885,970 | 9,889,272 | 3,303 |
ENST00000306084.6 | hg19 | chr18 | 9,885,973 | 9,888,150 | 2,178 |
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