THYN1 thymocyte nuclear protein 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 30 |
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
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 |
---|---|
SYNONYM | HSPC144 |
SYNONYM | MDS012 |
SYNONYM | MY105 |
SYNONYM | THY28 |
SYNONYM | THY28KD |
MIM | 613739 OMIM |
HGNC | HGNC:29560 HGNC |
Ensembl | ENSG00000151500 Ensembl |
AllianceGenome | HGNC:29560 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000392595.6 | hg38 | chr11 | 134,248,279 | 134,253,248 | 4,970 |
ENST00000392594.7 | hg38 | chr11 | 134,248,279 | 134,253,370 | 5,092 |
ENST00000341541.8 | hg38 | chr11 | 134,248,282 | 134,253,352 | 5,071 |
ENST00000352327.5 | hg38 | chr11 | 134,248,288 | 134,253,350 | 5,063 |
ENST00000392595.6 | hg19 | chr11 | 134,118,173 | 134,123,142 | 4,970 |
ENST00000392594.7 | hg19 | chr11 | 134,118,173 | 134,123,264 | 5,092 |
ENST00000341541.8 | hg19 | chr11 | 134,118,176 | 134,123,246 | 5,071 |
ENST00000352327.5 | hg19 | chr11 | 134,118,182 | 134,123,244 | 5,063 |
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