TMEM59L transmembrane protein 59 like
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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28 |
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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 | BSMAP |
SYNONYM | C19orf4 |
MIM | 617096 OMIM |
HGNC | HGNC:13237 HGNC |
Ensembl | ENSG00000105696 Ensembl |
AllianceGenome | HGNC:13237 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000262817.8 | hg38 | chr19 | 18,612,870 | 18,621,039 | 8,170 |
ENST00000600490.5 | hg38 | chr19 | 18,607,430 | 18,621,039 | 13,610 |
ENST00000600490.5 | hg19 | chr19 | 18,718,240 | 18,731,849 | 13,610 |
ENST00000262817.8 | hg19 | chr19 | 18,723,680 | 18,731,849 | 8,170 |
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