TAGLN2 transgelin 2
Clinical Significance
MGeND | ClinVar | |
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Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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20 |
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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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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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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 | HA1756 |
MIM | 604634 OMIM |
HGNC | HGNC:11554 HGNC |
Ensembl | ENSG00000158710 Ensembl |
AllianceGenome | HGNC:11554 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000368096.5 | hg38 | chr1 | 159,918,107 | 159,923,717 | 5,611 |
ENST00000368097.9 | hg38 | chr1 | 159,918,111 | 159,925,507 | 7,397 |
ENST00000320307.8 | hg38 | chr1 | 159,918,777 | 159,924,551 | 5,775 |
ENST00000368096.5 | hg19 | chr1 | 159,887,897 | 159,893,507 | 5,611 |
ENST00000368097.9 | hg19 | chr1 | 159,887,901 | 159,895,297 | 7,397 |
ENST00000320307.8 | hg19 | chr1 | 159,888,567 | 159,894,341 | 5,775 |
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