TLX2 T cell leukemia homeobox 2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 28 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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34 |
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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
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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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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 |
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Target data | : |
MGeND data only
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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 | HOX11L1 |
SYNONYM | NCX |
MIM | 604240 OMIM |
HGNC | HGNC:5057 HGNC |
Ensembl | ENSG00000115297 Ensembl |
AllianceGenome | HGNC:5057 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000621092.1 | hg38 | chr2 | 74,513,559 | 74,516,761 | 3,203 |
ENST00000233638.8 | hg38 | chr2 | 74,514,450 | 74,517,148 | 2,699 |
ENST00000621092.1 | hg19 | chr2 | 74,740,686 | 74,743,888 | 3,203 |
ENST00000233638.8 | hg19 | chr2 | 74,741,577 | 74,744,275 | 2,699 |
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