TREX2 three prime repair exonuclease 2
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 12 |
Likely benign | 0 | 42 |
Conflicting classifications of pathogenicity | 0 | 2 |
not provided | 6 | 0 |
Uncertain significance | 0 | 84 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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2 |
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130 |
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6 |
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 |
---|---|
MIM | 300370 OMIM |
HGNC | HGNC:12270 HGNC |
Ensembl | ENSG00000183479 Ensembl |
AllianceGenome | HGNC:12270 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000338525.7 | hg38 | chrX | 153,444,473 | 153,470,587 | 26,115 |
ENST00000370231.3 | hg38 | chrX | 153,444,473 | 153,446,056 | 1,584 |
ENST00000370232.4 | hg38 | chrX | 153,444,473 | 153,470,587 | 26,115 |
ENST00000370212.5 | hg38 | chrX | 153,444,720 | 153,447,863 | 3,144 |
ENST00000393862.7 | hg38 | chrX | 153,444,473 | 153,447,863 | 3,391 |
ENST00000330912.7 | hg38 | chrX | 153,444,473 | 153,470,587 | 26,115 |
ENST00000334497.7 | hg38 | chrX | 153,444,473 | 153,470,587 | 26,115 |
ENST00000393862.2 | hg19 | chrX | 152,710,178 | 152,713,321 | 3,144 |
ENST00000330912.2 | hg19 | chrX | 152,710,178 | 152,736,045 | 25,868 |
ENST00000338525.2 | hg19 | chrX | 152,710,178 | 152,736,045 | 25,868 |
ENST00000334497.2 | hg19 | chrX | 152,710,178 | 152,736,045 | 25,868 |
ENST00000370232.1 | hg19 | chrX | 152,710,178 | 152,736,045 | 25,868 |
ENST00000370231.2 | hg19 | chrX | 152,710,178 | 152,711,945 | 1,768 |
ENST00000402951.1 | hg19 | chrX | 152,710,178 | 152,713,321 | 3,144 |
ENST00000414588.1 | hg19 | chrX | 152,710,178 | 152,713,321 | 3,144 |
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