TMEM98 transmembrane protein 98
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 6 |
Benign | 0 | 6 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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2 |
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28 |
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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
[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 | TADA1 |
MIM | 615949 OMIM |
HGNC | HGNC:24529 HGNC |
Ensembl | ENSG00000006042 Ensembl |
AllianceGenome | HGNC:24529 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000578289.5 | hg38 | chr17 | 32,928,204 | 32,945,106 | 16,903 |
ENST00000579849.6 | hg38 | chr17 | 32,928,153 | 32,944,315 | 16,163 |
ENST00000394642.7 | hg38 | chr17 | 32,927,910 | 32,941,613 | 13,704 |
ENST00000394642.7 | hg19 | chr17 | 31,254,928 | 31,268,631 | 13,704 |
ENST00000579849.6 | hg19 | chr17 | 31,255,171 | 31,271,333 | 16,163 |
ENST00000578289.5 | hg19 | chr17 | 31,255,222 | 31,272,124 | 16,903 |
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